{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8521485002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6403702002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8521485002,"updated_at":"2026-04-23T15:57:11-04:00","requisition_id":"219 - 2026 - 004","title":"Associate Director / Director, Data Management","company_name":"Beam Therapeutics","first_published":"2026-04-23T15:51:52-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Senior Director, Clinical Data Management, the Associate Director / Director, Clinical Data Management will serve as the dedicated data management lead for our Liver franchise. Initially supporting a single study within the program, this individual will grow with the franchise as it expands to include additional studies within the same program and, ultimately, other programs across the franchise portfolio.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role offers a unique blend of hands-on study oversight and strategic leadership, making it an ideal opportunity for a candidate who thrives at the intersection of execution and innovation, in a fast‑paced biotech environment where clarity, quality, and collaboration are critical.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a highly visible role working cross‑functionally with Clinical Development, Biostatistics, Statistical Programming, Regulatory, Quality, and external partners to ensure data integrity, inspection readiness, and timely delivery of data supporting key development and regulatory milestones.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Primary Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Program \u0026amp;amp; Study Ownership\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead sponsor side clinical data management activities across multiple concurrent studies within a defined therapeutic area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own data management execution from study start-up through database lock and archival for concurrent studies, including late stage and registrational trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure data quality, integrity, and traceability to support interim analyses, CSRs, DSURs, IB updates, and program specific regulatory interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify data risks, trends, and operational dependencies; communicate issues early with clear, solution-oriented recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;CRO \u0026amp;amp; Vendor Oversight\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary data management contact for CROs and third-party data vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee outsourced CDM activities to ensure timely, high-quality deliverables aligned with sponsor’ expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor CRO and vendor performance, escalating risks and proposing mitigation strategies in partnership with the Senior Director of Data Management.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Data Standards, Systems \u0026amp;amp; Process Contribution\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute expert input to the development and evolution of data management standards, processes, tools/systems and vendor operating models as the organization scales its clinical portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide hands-on leadership for:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;CRF design and cross functional review\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Edit check specifications and user acceptance testing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Management Plans and CRF Completion Guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;External data transfer specifications\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Apply CDASH/CDISC expertise and partner with Statistical Programming to support SDTM readiness, validation outputs, Reviewer’s Guides, and define.xml.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Inspection Readiness\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support inspection readiness activities across assigned programs, ensuring documentation and data traceability meet regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key data management participant during audits and inspections, in coordination with the Senior Director and Quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure data management deliverables remain inspection ready throughout the study lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Cross-Functional Partnership\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, Regulatory, and Quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate complex data issues clearly and effectively to stakeholders with varying technical backgrounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build trust as a pragmatic, detail-oriented partner who balances scientific rigor with efficient execution.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS or MS degree in a scientific or health-related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in clinical data management within pharmaceutical/biotech and/or CRO environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated sponsor-side ownership of Phase I, II and III studies, from start-up through closure for multiple clinical studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong hands-on experience with EDC systems (e.g., Medidata RAVE, Veeva EDC, Oracle Inform).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of CDASH/CDISC, GCP/ICH, and FDA regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience overseeing CROs and external data vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing reports using J-Review and/or other CDM reporting tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior IND, as well as NDA/BLA (filing/submission) experience, is highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be self-motivating, with strong analytical, organizational, and communication skills, with the ability to manage complexity across multiple studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to navigate evolving priorities and drive timelines forward with focus and composure in a fast-moving organization.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience and knowledge of gene/cell therapy and/or rare disease.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience supporting registrational or pre registrational programs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$185,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4071033002,"name":"Biometrics","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8501507002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6395925002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8501507002,"updated_at":"2026-05-14T16:30:51-04:00","requisition_id":"218 - 2026 - 001","title":"Associate Director / Director, Toxicology","company_name":"Beam Therapeutics","first_published":"2026-04-23T15:28:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is looking for a highly talented and motivated \u0026lt;strong\u0026gt;Associate Director / Director, Toxicology\u0026lt;/strong\u0026gt; to join our growing Non-Clinical Development team.\u0026amp;nbsp; The \u0026lt;strong\u0026gt;Associate Director / Director, Toxicology\u0026lt;/strong\u0026gt; will be responsible for the nonclinical safety assessments supporting Beam\u0026#39;s discovery and development programs. The right candidate will be responsible and accountable for the design and execution of safety studies for discovery to early/late development programs. Additionally, this role will be accountable for the authoring of documents for regulatory filings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work cross-functionally to drive nonclinical safety related activities from discovery through regulatory filings and to commercialization for various programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and oversee the execution of phase appropriate nonclinical safety strategies along with integrated project plans including milestones, timelines, resources and budgets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate interactions with CRO\u0026#39;s, in collaboration with the Nonclinical Development Operations group, to ensure delivery of study results and reports consistent with program timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic contribution as the subject matter expert for GLP, non-GLP, and safety pharmacology studies supporting development and platform programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide toxicology support for regulatory submissions and interactions with health authorities, including the authoring of nonclinical safety sections of US and international regulatory applications, and help resolve nonclinical safety queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive and be accountable for delivery of high-quality safety reports to ensure clinical plans and regulatory filing submissions in multiple markets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the toxicology representative in cross-functional meetings both internally and externally.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ph.D. with 8+ years of scientific experience OR MS with 12+ years of scientific experience. BS with 15+ years of scientific experience in pathology will also be considered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with LNPs and/or gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting IND-enabling studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to develop and deliver clear and concise presentations for both internal and external meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of all aspects of nonclinical safety and experience with regulatory filings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive knowledge of relevant FDA and EMEA regulations and processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated proven experience in working with CROs for protocol design and study execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with cross-functional and collaborative project teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate effectively within an innovative and science-driven company environment; delivery-oriented, able to inspire others, driven and hands-on with unquestionable integrity and the highest ethical standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Candidates are expected to come onsite 1-3 days per week.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$185,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4040022002,"name":"Toxicology","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8548782002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6414594002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8548782002,"updated_at":"2026-05-18T10:48:33-04:00","requisition_id":"312 - 2026 - 003","title":"Associate Director, Product Quality Assurance ","company_name":"Beam Therapeutics","first_published":"2026-05-18T10:46:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director of Product Quality for Cell and Gene Therapy Programs will act as a leader in the Quality organization and will support the quality aspects of Beam’s programs over the holistic product lifecycle. This position acts as a Quality Leader by supporting Product Quality Leads (PQLs) on program and CMC-focused deliverables and is a strategic partner with CMC functional areas across the product lifecycle.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position will have a direct impact on the product quality strategy and overall lifecycle management aspects, from an end-to-end quality perspective (development to post-commercialization). Working closely with the assigned PQLs, the role supports consistency and quality of content and product strategy across the CMC spectrum including review of CMC technical content provided for global clinical and commercial regulatory submissions as well as associated quality records. \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provides strategic Quality CMC-focused support based on Program Team timelines, milestones, and regulatory commitments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives and takes action on Phase Appropriate Quality strategy for Beam’s products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs Quality review/approval of records and documentation related to manufacturing such as process defining documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs product quality impact assessments for product complaints, manufacturing deviations, OOT/OOS results, MRB, adverse trends, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality reviewer and approver of select technical documents (e.g. complaints, temperature excursion reports, justification of specification (JoS), specifications, method validations, critical quality attribute (CQA) assessment, comparability, risk assessments, continued process verification (CPV), tech transfer, ad hoc testing / characterization protocols, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ad hoc Quality representative on Program Team and CMC Team in support of primary PQL.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures alignment with regulatory requirements, industry standards / best practices, and Beam initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical to commercial analytical control strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic and technical support across product lifecycle (manufacturing process and analytical method changes, tech transfer, characterization, comparability, validations, technology improvements, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reviews manufacturing process performance, analytical method performance, stability data, etc. for signals / trends / patterns to proactively monitor and if necessary, support mitigations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Authors annual product quality reviews.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responds to compliance \u0026amp;amp; quality related troubleshooting activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports expiry extensions in collaboration with QC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists in the implementation of quality systems and procedures/SOPs as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enables alignment of product transition from clinical to commercial phase and tech transfers between sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proposes product improvement activities related to overall quality and compliance strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality reviewer for select CMC technical content provided for global clinical and commercial regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support due diligence audits, site selection, and qualification of external partners as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports other members of the Quality Team and organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports Quality Risk Management (QRM) program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs other tasks and assignments as needed and specified by management.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelors or Advanced degree in scientific discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12+ years’ experience in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and/or quality with at least 4 years of which should have been in a CMC-focused position in Cell and Gene Therapy Quality role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detailed knowledge and understanding of GMP regulations and Food and Drug Administration (FDA) requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to influence without direct authority.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to develop into a primary PQL for Beam programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills, detail-oriented personality and ability to work and drive change across functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience interacting with regulatory health authorities at pre- and post-approval inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong team player that has a customer service approach and is solution oriented.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent listening, communication and interpersonal skills fostering team spirit.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Consistent delivery of high-quality work at all times.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Candidates are expected to come onsite to our Cambridge, MA site 1-3 days per week.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$185,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$225,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052903002,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545673002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413364002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8545673002,"updated_at":"2026-05-12T11:52:44-04:00","requisition_id":"312 - 2026 - 007","title":"Associate Director, Quality Control Technical Services","company_name":"Beam Therapeutics","first_published":"2026-05-12T11:51:04-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an Associate Director, Quality Control Technical Services to lead QC CMC strategy for our ex vivo cell therapy franchise, spanning late-stage development, initial commercial launch, and ongoing lifecycle management. This role will also play a critical leadership role in defining and executing the strategy for mRNA drug substance and critical materials platforming, supporting both current programs and future pipeline scalability.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful candidate will work cross‑functionally with Analytical Research \u0026amp;amp; Development, Bioprocess Development, Manufacturing Technical Services, Manufacturing Operations, Regulatory Affairs, and Quality Assurance to drive the transfer, qualification, validation, and lifecycle management of analytical methods for gene‑edited cell therapy products and associated critical materials (e.g., mRNA). These efforts will ensure analytical readiness to support regulatory submissions, agency approvals, and commercial supply.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role will be instrumental in defining the QC testing and technical transfer strategy for next‑generation autologous cell therapy manufacturing, including the transfer of automated and validated analytical methods to Beam’s internal manufacturing facility. A key focus will be the internalization of validated mRNA methods into the North Carolina Quality Control laboratory, strengthening in‑house testing capabilities and long‑term operational resilience.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In addition, this position will contribute directly to regulatory filings, including specifications, analytical method validation reports, and CMC documentation, and will serve as a QC technical subject matter expert across program teams to ensure compliant, robust, and phase‑appropriate analytical strategies.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Primary Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and influence QC CMC strategy in partnership with cross‑functional CMC teams for master cell banks (MCBs), plasmids, and mRNA drug substance and critical materials, supporting both ex vivo and in vivo therapy programs across development and commercialization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and execute the QC testing, method strategy, and technical execution to enable next‑generation autologous cell therapy manufacturing processes, including analytical readiness for process validation, comparability, and technology transfer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and coordinate analytical method transfer, qualification, and validation activities across internal and external QC laboratories, ensuring compliant, phase‑appropriate, and inspection‑ready execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain analytical control strategies by tracking and trending in‑process, release, and stability data, collaborating with statisticians and program teams to define and justify specifications for MCBs, plasmids, mRNA, and autologous cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and oversee stability strategies and programs for MCBs, plasmids, mRNA, and ex vivo cell therapy products, ensuring alignment with regulatory expectations and lifecycle needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead analytical method lifecycle management for late‑stage and commercial ex vivo portfolio, including method performance monitoring, remediation, comparability activities, and continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive the internalization of validated mRNA analytical methods into Beam’s North Carolina Quality Control laboratory, strengthening internal capabilities and supporting long‑term commercial supply.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review Quality System documentation, including SOPs, Change Controls, and CAPAs, to support method implementation, lifecycle changes, and inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Regulatory Affairs–CMC to author, review, and coordinate CMC sections of regulatory submissions, including specifications, method validation reports, and responses to agency queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure QC visibility and alignment on regulatory interactions, including tracking agency questions, commitments, post‑approval requirements, and method introduction or change strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key QC technical interface across CMC, Quality, Regulatory, Manufacturing, Process Development, Analytical Research \u0026amp;amp; Development, and external partners, providing clear guidance, alignment, and issue resolution to advance program milestones.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (MS, Ph.D) in Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline, with 8+ years of relevant industry experience in Quality Control, Analytical Development, or CMC within biologics, cell therapy, or gene therapy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive hands‑on experience with ex vivo autologous cell therapies, including CD34+ cell‑based products, across late‑stage development, validation, and/or commercial readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated technical expertise in cell handling and testing methodologies, including functional and potency assays, flow cytometry, NGS‑based assays, and separation sciences. Experience with analytical method automation, qualification, and validation is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven understanding of analytical method lifecycle management, including method transfer, qualification, validation, performance monitoring, remediation, and comparability, particularly for late‑stage and commercial products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of US and EU regulatory expectations (e.g., FDA/CBER, EMA, ICH, USP) applicable to cell and gene therapy CMC, with the ability to apply guidance in a phase‑appropriate and inspection‑ready manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience supporting regulatory submissions (INDs, BLAs, amendments, post‑approval changes) for cell and gene therapy products, including specifications, method validation reports, and responses to health authority questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead and influence cross‑functional program teams, partnering effectively with CMC, Manufacturing, Analytical R\u0026amp;amp;D, Quality Assurance, and Regulatory Affairs in a fast‑paced, matrixed environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and leadership skills, with a track record of clearly articulating technical strategies, aligning stakeholders, and driving decisions across functions and with external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Documented success in driving complex, program‑critical initiatives to completion on time and within budget, including managing dependencies, risks, and priorities across multiple workstreams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly developed organizational, analytical, and problem‑solving skills, with the ability to interpret complex datasets, assess risk, and translate data into actionable QC and CMC strategies.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$185,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$225,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052903002,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8378438002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6345129002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8378438002,"updated_at":"2026-04-10T13:51:45-04:00","requisition_id":"519 - 2026 - 001","title":"Corporate Counsel/Senior Corporate Counsel, Commercial Contracts","company_name":"Beam Therapeutics","first_published":"2026-01-21T10:13:47-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is seeking a highly skilled attorney to serve as the Corporate Counsel/Senior Corporate Counsel, Commercial Contracts. This role will partner with Beam’s medical affairs, commercial and manufacturing teams to provide contracting support for Beam’s transition to a commercial stage company. Ideal candidates will excel in negotiating complex agreements, managing risk, and achieving business objectives in a fast-paced, cutting-edge biotechnology company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Draft and negotiate high-stakes agreements in support of Beam’s anticipated product launches, including complex commercial contracts with gene therapy treatment centers, channel partners and manufacturers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with legal review of other pre-commercial activities, including advisory boards, patient engagement events, patient support programs, market access activities, speaker programs, and market research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide legal support to Beam’s various promotional material review committees.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing contracting support and lifecycle management, including agreement interpretation and risk analysis, for Beam’s commercial, medical affairs, manufacturing and other teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with business teams and subject matter experts on continuous review and updates of Beam contracting playbooks and standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft and negotiate a range of other key agreements in support of Beam’s broader business, including clinical trial agreements, material transfer agreements, sponsored research agreements, service provider agreements, and non-disclosure agreements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Juris Doctor (JD) from an accredited law school; admission to practice in at least one U.S. jurisdiction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of experience with complex biotechnology contracting, ideally with commercial-stage cell and gene therapy companies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple, overlapping, high-stakes agreements to completion on tight timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible, must be able to work collaboratively with team members for a diverse range of projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High degree of professional ethics and integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgement and ability to quickly analyze different sources of information.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Practical and business-minded, capable of recognizing, assessing, and responding to urgent matters with timely, pragmatic, and clear solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional and demonstrated written and verbal communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Candidates are expected to come onsite 2 days per week.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Additive Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience advising medical affairs and commercial teams on legal and regulatory legal requirements related to product launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to provide legal counsel on health care laws, such as anti-kickback, false claims and transparency statutes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Service on promotional material review committees for pre-commercial or commercial biotechnology companies.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$320,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4040007002,"name":"Legal","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545486002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413285002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8545486002,"updated_at":"2026-05-14T11:22:50-04:00","requisition_id":"420 - 2026 - 035","title":"Director, HCP Marketing","company_name":"Beam Therapeutics","first_published":"2026-05-14T11:22:50-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director, HCP Marketing will be a critical member of the Commercial team and will be responsible for leading the healthcare professional (HCP) engagement strategy to support the launch of Beam asset in Sickle Cell Disease. This role will focus on identifying, understanding and engaging key HCP segments. This individual will partner closely with the cross-functional partners such as key account managers, medical affairs, patient operations and market access, to ensure aligned, and impactful engagement with the HCP community. Through the development of targeted promotional strategies and educational initiatives, this individual will help drive informed clinical dialogue and support successful product adoption at launch.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;This is a unique opportunity for a strategic, collaborative, and results-oriented HCP marketer to build a high-impact engagement platform in a complex and underserved therapeutic area.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Responsible for the management of the agency of record, contributes to the development of brand strategy, develop and deploy unbranded and branded educational materials and engagement tools across personal and non-personal channels.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with account leads to align field strategies, deliver compelling resources, ensure consistent and aligned execution across regions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create field-facing resources, engagement tools and training (e.g., leave-behinds, visual aids, digital content, trainings, etc.) that support effective HCP conversations and reinforce key messages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the planning and execution of HCP-focused conference activities, including booth presence, branded and unbranded materials, and sponsored programs in collaboration with cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive the planning and execution of advisory boards including associated content development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee tracking of HCP marketing budget accruals, forecasts, and actuals, and ensure successful and timely completion of projects within budget.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help manage external agencies and partners to ensure timely, high-quality deliverables that meet agreed-upon objectives, key performance indicators (KPIs), timelines, and budgets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with all Medical, Legal, and Regulatory (MLR) requirements in the development and deployment of HCP-facing materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage customer and market insights, claims, and performance data to develop insight-driven marketing strategy and content, continuously optimize programs and identify opportunities for innovation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree with 10+ years of pharmaceutical or biotech experience, with at least 3 years focused on US HCP Marketing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cell \u0026amp;amp; Gene Therapies experience is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting and partnering with field teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to translate complex clinical information into clear, compelling promotional messaging for HCP audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management and organizational skills, with the ability to lead multiple high-priority initiatives simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively managing external partners, agencies and budgets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Navigate Medical, Legal, and Regulatory (MLR) review and approval processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, strategic thinking, relationship-building skills, and a results-oriented mindset.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Onsite requirements: Candidates are expected to come onsite 1-3 days per week.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4073329002,"name":"Commercial Strategy","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8435669002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6369554002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8435669002,"updated_at":"2026-04-16T16:37:04-04:00","requisition_id":"420 - 2026 - 006","title":"Director, Insights \u0026 Analytics","company_name":"Beam Therapeutics","first_published":"2026-02-24T13:27:36-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is looking for a highly motivated and experienced Insights \u0026amp;amp; Analytics leader to expand our commercial capabilities as we advance our portfolio toward potential commercialization.\u0026amp;nbsp; The Director, Insights \u0026amp;amp; Analytics will lead the development and execution of market insights, forecasting, and competitive intelligence capabilities across Beam’s portfolio. This role will serve as a strategic partner to Marketing, Market Access, Patient Operations, Medical Affairs, and Portfolio Strategy to translate key business questions into actionable insights that inform decision-making across the product lifecycle. \u0026amp;nbsp;In addition, the Director, Insights \u0026amp;amp; Analytics will directly support early pipeline assets, e.g. provide market sizing, competitive landscape analyses, drivers for therapy and brand choice.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position requires both strategic thinking and hands-on execution in a fast-moving, cross-functional environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Market Insights \u0026amp;amp; Research Leadership\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and lead market research capability across the portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Marketing, Market Access, Medical Affairs, and Portfolio Strategy to define key business questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recommend appropriate market research methodologies and lead RFP processes and vendor selection for market research projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage external research partners and ensure high-quality execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop initial discussion guides, surveys, and stimuli in collaboration with cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize research findings into clear, actionable insights and facilitate cross-functional sharing.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Forecasting \u0026amp;amp; Analytical Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead forecasting processes across the portfolio, including:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Patient flow and demand models\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Market uptake scenarios\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sensitivity analyses and risk scenarios\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain analytical tools and models to support asset-level and portfolio-level decision making.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Competitive Intelligence\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish and lead competitive intelligence processes across the portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor competitive clinical, regulatory, and commercial developments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage external CI vendors and spearhead CI strategy and coverage for conferences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Synthesize competitive insights into implications for strategy, positioning, and planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support scenario planning and strategic trade-off discussions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Early Pipeline \u0026amp;amp; Portfolio Analyses\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support early-stage assets with:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Epidemiology and market sizing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competitive landscape assessments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unmet need and treatment paradigm analyses\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Possibly facilitate early asset TPP generation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA in a relevant academic field; MBA, MD, PhD, or other graduate degree strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;15+ years business experience within the pharma/biotech/biopharma space or consulting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in cell and gene therapy is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of primary and secondary market research methodologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience leading vendor selection and managing research partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be capable of managing and prioritizing multiple activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on forecasting experience, including scenario planning, strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to synthesize complex data into clear strategic insights.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional collaboration skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable operating in ambiguity and building new processes from scratch.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and executive presentation skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Role is based in Cambridge, MA.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Onsite requirements: Candidates are expected to come onsite 1-3 days per week.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel 25% as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4073329002,"name":"Commercial Strategy","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545723002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413381002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8545723002,"updated_at":"2026-05-14T11:54:26-04:00","requisition_id":"251 - 2026 - 012","title":"Director, Medical Information","company_name":"Beam Therapeutics","first_published":"2026-05-14T11:48:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is seeking a driven and scientifically rigorous \u0026lt;strong\u0026gt;Director of Medical Information\u0026lt;/strong\u0026gt; to build and lead the Medical Information (MI) function. This is a hands-on leadership role well-suited to a motivated individual contributor and emerging leader who is passionate about establishing strong operational foundations and delivering high-quality scientific content in the rare disease space. The \u0026lt;strong\u0026gt;Director of Medical Information\u0026lt;/strong\u0026gt; will design and implement core MI capabilities — including inquiry management systems, standard response documents, and medical review workflows — positioning the organization for its first commercial launch and scaling for future clinical programs. The \u0026lt;strong\u0026gt;Director of Medical Information\u0026lt;/strong\u0026gt; will also play an active role in the company\u0026#39;s Medical Affairs AI initiatives, contributing scientific and operational expertise to the responsible deployment of AI-enabled tools for content generation and knowledge management.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish the Medical Information department from the ground up, including defining the operating model, staffing plan, technology infrastructure, and standard operating procedures (SOPs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain the MI quality framework to ensure all scientific content meets regulatory, compliance, and scientific integrity standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the internal subject matter expert on medical information best practices, regulatory expectations (FDA, EMA), and industry benchmarks for rare disease and advanced therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and oversee the medical review process for promotional and non-promotional materials, ensuring scientific accuracy and alignment with label and clinical data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner in the establishment of a Medical Review Committee (MRC) / Promotional Review Committee (PRC), collaborating closely with Regulatory Affairs, Legal, and Commercial teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain a comprehensive library of standard response documents (SRDs), custom responses, and medical FAQs covering the company\u0026#39;s cell and gene therapy pipeline across rare disease indications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review medical information letters, disease education materials, clinical summaries, and scientific dossiers for internal and external use.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all MI content reflects the most current evidence base, including clinical trial data, real-world evidence, and peer-reviewed literature.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Science Liaisons (MSLs), Clinical Development, and Commercial teams to develop scientifically rigorous training materials, slide decks, and internal reference tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the development of pipeline and disease area resources that enable cross-functional teams to communicate accurately about the science of cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to publication planning and medical education initiatives, supporting the Medical Affairs strategy for pre-launch and post-launch activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Patient Advocacy and Medical Communications to ensure content is accessible, accurate, and patient-centered.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute as a Medical Affairs subject matter expert to the company\u0026#39;s AI strategy, partnering with Data Science, IT, and Medical Affairs leadership to evaluate and implement AI-enabled solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the design and validation of AI-assisted medical information tools, including intelligent response generation, literature surveillance automation, and content quality-checking workflows.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in establishing governance frameworks for responsible AI use in medical communications, including bias assessment, hallucination mitigation, and compliance review protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor the evolving regulatory and industry landscape around AI in medical affairs (e.g., FDA guidance, ISPE, PhRMA frameworks) and translate insights into actionable policies.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced scientific degree required: PharmD, MD, PhD, or equivalent in life sciences, pharmacy, or a related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 7 years of experience in Medical Information, Medical Affairs, or Medical Communications within the pharmaceutical or biotechnology industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience contributing to or building Medical Information capabilities, including SOP development and content library management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid working knowledge of medical review processes (MRC/PRC) and promotional/non-promotional content review, with familiarity with applicable FDA and EMA regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific writing skills with experience developing SRDs, medical information responses, and clinical content for internal and external audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work effectively cross-functionally in a fast-paced, pre-commercial biotech environment with lean teams and evolving priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interest in or exposure to rare disease therapeutic areas, including the scientific and operational challenges of small patient populations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in cell and gene therapy, gene editing, or other advanced therapy medicinal products, preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to AI/ML applications in Medical Affairs or Medical Information, including prompt engineering, LLM evaluation, or AI governance, preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with medical information platforms (e.g., Veeva Vault, Salesforce Health Cloud, MedAnswers) or emerging AI-powered MI solutions, preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting pre-BLA/pre-NDA activities or commercial launch readiness for orphan-designated or first-in-class therapies, preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Onsite requirements: Must be able to work onsite as required and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4099201002,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545535002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413309002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8545535002,"updated_at":"2026-05-19T10:37:06-04:00","requisition_id":"420 - 2026 - 036","title":"Director, Patient Marketing","company_name":"Beam Therapeutics","first_published":"2026-05-19T10:35:11-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director, Patient Marketing will be a critical member of the Marketing team and will be responsible for the development and execution of patient-focused campaigns for Beam’s asset in Sickle Cell Disease. This leader will shape our digital and patient engagement strategy, driving innovative, compliant, and impactful programs that empower patients and caregivers throughout their journey.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;This is a unique opportunity for a strategic, collaborative, and results-oriented Patient marketer to build a high-impact engagement platform in a complex and underserved therapeutic area.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;The Director, Patient Marketing will collaborate closely with cross functional partners—including HCP Marketing, Patient Advocacy, Patient Services, Medical Affairs, Regulatory, Legal, Field Teams, and external partners—and will play a critical role in the execution of the brand strategy at launch and beyond.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the end-to-end patient marketing strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute multi-channel campaigns across digital, social, print, and in-person channels, ensuring alignment with overall brand objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive innovation in digital engagement, including websites, SEO/SEM, social media, email, and emerging technologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee creation of patient-facing materials and programs, collaborating with creative agencies, digital partners, and cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Spearhead patient ambassador program, collaborating with compliance and legal teams to drive high impact tactics with patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage branded product websites as well as digital interface to patient support services program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct research and analytics efforts to understand patient needs, preferences, and digital behaviors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor campaign performance, track KPIs, and optimize programs based on data-driven insights.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all initiatives are compliant with medical/legal/regulatory (MLR) standards and corporate policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion ethical, patient-first communication that supports informed decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish effective partnership and collaboration with patient advocacy teams by ensuring clearly defined roles and remit on cross functional patient tactics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Integrate advocacy perspectives into strategic planning deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Patient Services \u0026amp;amp; Patient Operations team to optimize patient communications and engagement.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree with 10+ years of pharmaceutical or biotech experience, with at least 5 years focused on US Patient Marketing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sickle Cell Disease and Cell \u0026amp;amp; Gene Therapies experience is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting and partnering with field teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with new product launches, or major indication launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven expertise in digital marketing, patient engagement strategies, and multi-channel campaign execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience with patient ambassador programs, their development, compliance/legal considerations, and ability to make strategic decisions on investment choices across tactics involving ambassadors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of patient journeys in Sickle Cell Disease or other rare diseases and the role of patient/caregiver engagement in driving outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effectively managing external partners, agencies and budgets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to navigate Medical, Legal, and Regulatory (MLR) review and approval processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, strategic thinking, relationship-building skills, and a results-oriented mindset.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional communication, collaboration, and influence skills with senior leaders and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical mindset with the ability to translate insights into actionable strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfort working in a dynamic, fast-paced environment with multiple priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated strategic thinking ability to support enterprise needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Onsite requirements: Candidates are expected to come onsite 1-3 days per week\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4073329002,"name":"Commercial Strategy","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8492835002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6392281002,"location":{"name":"Cambridge, MA / Durham, NC"},"metadata":null,"id":8492835002,"updated_at":"2026-04-10T13:52:34-04:00","requisition_id":"334 - 2026 - 003","title":"Director / Senior Director, Global Logistics, Warehousing and Trade Compliance","company_name":"Beam Therapeutics","first_published":"2026-04-02T16:17:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Senior Director, Global Logistics, Warehousing and Trade Compliance\u0026lt;/strong\u0026gt; is responsible for defining and executing the global strategy, operational leadership, and compliant storage and movement of materials supporting R\u0026amp;amp;D, Clinical, and Commercial programs across Beam. This role provides end‑to‑end leadership across global logistics operations, warehousing networks, and trade compliance, ensuring reliable supply, regulatory adherence, and scalable infrastructure to support pipeline growth and commercialization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This position reports to the Vice President, Supply Chain and serves as a key member of the Supply Chain Leadership team, partnering closely with Technical Operations, Quality, R\u0026amp;amp;D, Finance, Legal, Procurement, Clinical Patient Supply and Commercial Patient Operations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Global Logistics: \u0026lt;/strong\u0026gt;Provides operational and strategic leadership for all R\u0026amp;amp;D, Clinical, and Commercial shipments. Serves as subject matter expert for ambient, low‑temperature, and ultra‑low‑temperature cold chain systems, including shipping systems qualification and lane validation, in support of CMC development and commercialization. Supports Commercial Patient Operations for Risto-cel Patient shipments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Warehousing: \u0026lt;/strong\u0026gt;Leads internal warehouse operations and the global 3PL network supporting storage, inventory management, kitting, and production support for critical raw materials, drug substance, and drug product. Ensures inventory accuracy, material availability, and scalable warehouse capabilities aligned with clinical and commercial demand.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Trade Compliance:\u0026lt;/strong\u0026gt; Acts as the enterprise risk leader for global trade compliance, ensuring compliance with international, federal, and state import/export laws and regulations. Leads the development and governance of compliant, efficient trade processes across North America, Europe, and Asia‑Pacific regions, and serves as the primary interface with customs brokers, government agencies, and external auditors. Champions a culture of compliance while enabling business agility and uninterrupted supply. Supports Market Access team for any commercial trade or channel distribution aspects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Strategy \u0026amp;amp; Leadership:\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute global logistics, warehousing, and trade compliance strategy to support R\u0026amp;amp;D, clinical trials, and commercial operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish long‑term vision for a flexible, scalable global distribution and storage network, aligned with Beam’s growth and commercialization plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a senior leader influencing enterprise and site‑level supply chain strategies, including readiness for new product launches and expansion of cell and gene therapy programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, lead, and develop high‑performing teams, fostering a strong talent pipeline, culture of accountability, and continuous improvement mindset.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Logistics Operations\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide operational leadership for global distribution, including domestic and international shipments from internal sites and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead shipping operations supporting R\u0026amp;amp;D, clinical, and commercial programs, ensuring on‑time, in‑full delivery and patient‑centric execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own cold chain strategy and execution, including qualification, validation, monitoring, and continuous improvement of shipping lanes and systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure logistics operations comply with GMP, GDP, EHS, product security, and data integrity requirements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Warehousing \u0026amp;amp; Inventory Management:\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead internal and external warehousing operations, including inventory control, materials management, kitting, and production support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure no disruption to production schedules while proactively identifying and mitigating supply risks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive inventory optimization, accuracy, and visibility across the network using ERP and digital tools.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Trade Compliance \u0026amp;amp; Governance\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Create, lead, and chair the Trade Compliance Committee, ensuring adherence to all applicable global import/export laws, regulations, and guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain a robust global import/export compliance framework, including permits, licenses, valuation, duties, VAT, sanctions, HTS classification, country of origin, and applicable Tariffs/Free trade agreements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as primary respondent to regulatory agency inquiries; investigate issues, develop corrective strategies, and ensure timely, compliant responses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead duty savings and optimization strategies in collaboration with Finance and Supply Chain, while maintaining full regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Performance, Financial \u0026amp;amp; Operational Excellence\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish and monitor KPIs across logistics, warehousing, and trade compliance with clear, data‑driven reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage operating budgets, capital expenditures, and cost optimization initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive automation, digitalization, and process improvements to enhance efficiency, scalability, and compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion lean principles, continuous improvement, and right‑first‑time execution across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Stakeholder \u0026amp;amp; External Engagement\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain strong partnerships with Legal, Finance, Clinical, Commercial, Quality, Manufacturing, Procurement, IT, and HR.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent the company with customs authorities, regulatory agencies, industry groups, and external counsel as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in global forums to influence policy, standardization, and best practices across the supply chain network.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Business, Supply Chain, Engineering, Life Sciences, or related field; MBA or Master’s degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;18+ years of progressive experience in global logistics, warehousing, supply chain, and/or trade compliance within biotech, pharmaceutical, or other highly regulated environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven senior leadership experience managing complex global networks of internal operations and external partners (CMOs, CDMOs, 3PLs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of global trade compliance regulations, including U.S. Customs and relevant international authorities; experience with permits, licenses, duties, VAT, sanctions, and duty savings strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise in pharmaceutical cold chain logistics (ambient, refrigerated, frozen, ultra-low temperature) across R\u0026amp;amp;D, clinical, and commercial programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic and operational leadership skills, with the ability to influence cross-functional and matrixed stakeholders globally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent analytical, communication, and decision-making skills in high-complexity environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Financial acumen including budgeting, cost control, and KPI management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with ERP systems (SAP preferred) and electronic Quality Management Systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relevant certifications or formal trade compliance training are preferred (e.g., Customs, Export Compliance, APICS, HAZMAT).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel / On-site Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Up to 20% travel required to support internal sites, external partners, and global supply chain initiatives.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Onsite requirements:\u0026lt;/strong\u0026gt; Must be able to work onsite daily and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$320,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4076374002,"name":"Supply Chain","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002},{"id":4036281002,"name":"Beam - NC","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545691002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413371002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8545691002,"updated_at":"2026-05-12T12:05:59-04:00","requisition_id":"312 - 2026 - 005","title":"Director / Senior Director, Quality Control Automation \u0026 Digitalization","company_name":"Beam Therapeutics","first_published":"2026-05-12T12:02:04-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a Director / Senior Director, Quality Control Automation and Digitalization to lead the strategic transformation of Quality Control operations through advanced automation and digital platforms. This role blends strategic leadership with deep hands-on technical expertise in laboratory automation, digital solutions, and GMP operations. The position will serve as the QC Automation Lead, responsible for overseeing and coordinating end‑to‑end automated analytical workflows across multiple functions, including Analytical Development, Automation, Computational Biology, Quality Control, Quality Assurance, Information Technology, and Validation. This leader will drive cross‑functional alignment to ensure streamlined processes and timely delivery of robust, compliant analytical methods and procedures in support of GMP testing. In addition, this role is accountable for implementing comprehensive training programs to strengthen QC capabilities in automated and digital platforms, ensuring scientific rigor, data integrity, and operational excellence. The Senior Director/Director will foster a culture of innovation and continuous improvement, positioning QC to support current and future portfolio and regulatory needs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Primary Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the QC Automation Lead, providing deep technical expertise and strong compliance acumen to design, deploy, and sustain automation and digital solutions supporting GMP analytical methods and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner strategically with cross‑functional stakeholders—including Analytical Development, Automation, Computational Biology, Quality Control, Quality Assurance, Information Technology, and Validation—to define and implement integrated, end‑to‑end automation workflows.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the full lifecycle of automated solutions, including instrumentation and software onboarding, qualification, and validation; robust script development and testing; and technical transfer, qualification, and validation of automated analytical methods. This includes complex modalities such as cell‑based functional assays, flow cytometry, ddPCR, ELISA, and NGS.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive alignment on deliverables and exit criteria across Research, Development, and Commercial phases, including pre-qualification package signoffs, SME training completion, and qualification package approvals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct and facilitate investigation and resolution of complex technical challenges related to automated systems, ensuring scientific rigor, data integrity, and compliance with GMP expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and implement comprehensive training programs to build QC capability and confidence in automated and digital platforms, ensuring strong scientific and technical understanding across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mentor and develop team members in the design, authoring, execution, and lifecycle management of automated analytical protocols within GMP environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain technical standards, best practices, and governance for automation scripting, validation documentation, system lifecycle management, and troubleshooting methodologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recruit, develop, and retain top talent with expertise in laboratory automation, liquid handling platforms, relevant programming languages, and cell and gene therapy analytical techniques.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a highly collaborative environment that effectively bridges scientific expertise, automation engineering, and regulatory compliance, enabling innovation while maintaining inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (PhD preferred) with 15+ years of relevant experience in Quality Control, laboratory automation, and pharmaceutical or biotechnology operations, including 8+ years in progressively responsible leadership roles with demonstrated advancement to Director‑level scope.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive hands‑on automation experience, including 8+ years working with liquid handling platforms (e.g., Hamilton, Tecan), with demonstrated expertise in script development, validation, troubleshooting, and lifecycle management within GMP environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven expertise integrating automated workflows with LIMS and other enterprise digital systems to support compliant data management and end‑to‑end process automation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep technical understanding of molecular biology, cellular, and immunoassay techniques, including transfection/transduction workflows, ddPCR/qPCR, flow cytometry, ELISA, and next‑generation sequencing (NGS).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong track record leading cross‑functional automation initiatives in regulated biopharmaceutical settings, including oversight of instrument and software IQ/OQ/PQ, analytical method qualification and validation, and method lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success in building, leading, and developing high‑performing technical teams, with a proven ability to mentor, coach, and retain top talent.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional communication and influence skills, with the ability to engage senior leadership and align diverse stakeholder groups around complex technical and operational initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic mindset with the ability to translate business and portfolio needs into scalable automation strategies, roadmaps, and executable plans.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$320,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052903002,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8549991002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6415009002,"location":{"name":"Cambridge, MA / Durham, NC"},"metadata":null,"id":8549991002,"updated_at":"2026-05-20T11:58:54-04:00","requisition_id":"334 - 2026 - 004","title":"Director, Supply Chain Planning","company_name":"Beam Therapeutics","first_published":"2026-05-14T11:35:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Global Supply Chain Planning \u0026amp;amp; Network Strategy leader will be responsible for the supply and raw material planning function, supply network design and optimization strategy, inventory ownership and ensuring a strong supply and raw materials plan handoff to internal and external partners. He/she will be accountable to ensure uninterrupted supply of clinical and future commercial products via Beam’s Clinical S\u0026amp;amp;OP process. This role will report to the VP of Supply Chain and partner with leadership in TechOps, ClinOps, Finance, CMC and Program Teams to lead short-term integrated production and raw materials planning and long-range strategic supply chain planning of Beam’s product portfolio. This role will partner with Patient Supply to secure clinical supply needs and with Commercial, CMC, Engineering and PD for commercial supply chain design and capabilities of late-stage clinical development programs. This role will be accountable for designing and implementing core capabilities that drive proactive modeling and decision analysis of supply network and product strategy including governance, S\u0026amp;amp;OP business processes and technology to support this work. The role will be responsible for developing and executing a global inventory management program to ensure raw and critical material availability at Beam NC \u0026amp;amp; CDMO mfg sites. The role will be integral to enhancing site planning and scheduling capabilities at Beam’s mfg site in Durham, NC and partnering with SAP business lead on further advancing technology capabilities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will have a demonstrated track record of leading in a dynamic environment.\u0026amp;nbsp; They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross functional relationships.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement supply chain analytics, planning, and resilience processes and policy across the global supply chain for all stages of the product lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and manage global end to end supply planning and network design as Beam transitions from clinical to commercial stage company over next few years.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures appropriate inventory, including design/policy for Raw and Critical Materials (pDNA, mRNA, gRNA, mAb, lipids), Drug Substance, Bulk Drug Product, and Finished Drug Product.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and manage S\u0026amp;amp;OP process. Collaborate cross-functionally with ClinOps and Program teams to ensure accurate demand forecasts and scenarios/analytics. Responsible for supply network analysis to support tactical and strategic decision making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with Finance, Program Teams, CMC and PD to ensure robust modeling of product and network scenarios to support decision-making in governance forums.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform risk-based review of supply chain in order to determine appropriate inventory levels. Communicate demand uncertainties or risks and develop options for optimizing supply network capacity and capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver a response plan for disruptive challenges.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that plan and capabilities of each CDMO and suppliers are adapted to minimize the risk of disruption and deliver an effective response to ensure resilience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure optimal economics, and adequate supply chain security in partnership with Finance for Budget, LRP and capital planning processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee team to develop supply chain strategies, bringing integrated solutions to the production network. Hire, develop and mentor staff as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct activities of all functions involved in planning, warehousing, logistics to ensure control of materials from the receipt of raw materials to the delivery of the finished product including inventory controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and publish metrics to reflect the effectiveness and efficiency of department activities including supply chain KPIs on inventory, responsiveness and costs. Implement KPIs that drives accountability and improvement in both operational and financial metrics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with NC Mfg to implement standardized site planning and scheduling processes and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in the design \u0026amp;amp; implementation of SAP Phase 3 and IT roadmap in preparation for commercial launch.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA degree in Business, Science, Engineering or related field with 15+ years of experience in global supply chain from pharma, biotech or cell \u0026amp;amp; gene therapy companies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior drug development, manufacturing, clinical operations experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Master\u0026#39;s degree or MBA preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Final title/scope of role will be commensurate with experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior management skills with leadership experience building and sustaining global teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Passion for patients, collaborative and effective leader.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced knowledge of contracts, negotiation, vendor management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of practical implications of Sarbanes-Oxley controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of continuous improvement methodologies and tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and facilitation skills, with high degree of customer focus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Focuses on immediate and urgent business needs while driving long term strategic plans and capability \u0026amp;amp; organizational development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides strategy, vision and direction regarding issues that may have company-wide impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Requires in-depth knowledge of the functional area, business strategies, and the company’s goals. Possesses industry-leading knowledge of sourcing direct materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise and track record in manufacturing and supply chain execution and oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert in standing up a formal S\u0026amp;amp;OP process. Extensive experience in supply chain planning, SAP ERP system, capacity modeling, supply network strategy and optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise and proven track record in supply chain risk management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses in-depth knowledge of industry and system best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid knowledge of regulatory requirements, regulatory guidances, including pharmaceutical GMPs and ICH guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current on Biopharma supply chain, manufacturing technologies, supplier network, CMO network, performance and capacity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses understanding and application of principles, concepts, practices, and standards for DS and DP manufacturing in the biopharma industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, negotiation, and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical skills and ability to clearly communicate at tactical and strategic level with team and Sr Management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a dynamic and challenging environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Some travel may be required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work onsite, not a remote role.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$210,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$260,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4076374002,"name":"Supply Chain","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002},{"id":4036281002,"name":"Beam - NC","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8416333002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6361679002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8416333002,"updated_at":"2026-04-29T11:06:58-04:00","requisition_id":"217 - 2026 - 005","title":"Manager/Senior Manager Regulatory Affairs – Advertising, Labeling, and Promotion","company_name":"Beam Therapeutics","first_published":"2026-02-10T12:13:07-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Manager/Senior Manager, Regulatory — Advertising, Labeling, and Promotion (ALP) is responsible for leading U.S. promotional regulatory strategy and supporting ex-U.S. needs across our gene editing portfolio. This role reports to the Director of Regulatory Labeling and serves as a key member of the Promotional Review Committee (PRC/MLR). The position ensures compliant, compelling, and scientifically accurate communications consistent with core labeling and regulatory requirements.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as Regulatory lead for PRC/MLR review of promotional, disease awareness, scientific exchange, HCP, and patient-directed materials for certain products, under the supervision of the Director of Regulatory Labelling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the lifecycle of core and regional labeling documents including updates, reviews, approvals, and submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure claims are truthful, non-misleading, balanced, and aligned with approved labeling and scientific evidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and submit FDA Form 2253 filings; maintain records and track OPDP correspondence in conjunction with regulatory operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure alignment with promotional materials with CCDS, USPI/PI, IFU, and patient labeling.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor FDA OPDP/CBER guidance\u0026#39;s, enforcement trends, and evolving U.S. regulations; educate internal teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development of SOPs, governance documents, training programs, and inspection readiness activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advise cross-functional partners on scientific substantiation, evidence gaps, and claims strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review digital and social media content for compliance with fair balance, risk proximity, and evolving digital standards.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in a scientific discipline required; advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years (Manager) 10+ years (Senior Manager) experience in Regulatory Advertising \u0026amp;amp; Promotion.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of FDA promotional regulations (FD\u0026amp;amp;C Act, 21 CFR 202.1, OPDP/OC, CBER/CDER).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on PRC/MLR experience and 2253 submission experience required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, cross-functional collaboration, and regulatory judgment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$130,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$190,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4040024002,"name":"Regulatory ","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545621002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413342002,"location":{"name":"Durham, NC"},"metadata":null,"id":8545621002,"updated_at":"2026-06-05T13:16:27-04:00","requisition_id":"332 - 2026 - 006","title":"Manufacturing Associate II / Senior Manufacturing Associate I  ","company_name":"Beam Therapeutics","first_published":"2026-05-12T17:39:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is looking for highly energetic \u0026lt;span class=\u0026quot;collapsed-field-text\u0026quot;\u0026gt;Manufacturing Associate II / Senior Manufacturing Associate I\u0026lt;/span\u0026gt;\u0026amp;nbsp;to support scaling of cGMP manufacturing at our RTP site. Reporting to the Supervisor of Manufacturing, the successful candidate will provide manufacturing, operational \u0026amp;amp; technical experience around Cell Therapy. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support multiple areas of GMP production, and lead most operations as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain strong relationships at the site and cross-functionally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages and maintains training qualifications for assigned operations, operates as lead trainer on most operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identifies and revises manufacturing documents (Equipment SOPs) as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drafts change controls as required and manages small projects for area.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs limited CQV required tasks when needed for any new plant expansions or upgrades.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operate in up to an ISO 5/Grade B environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/MS in Life Sciences or Engineering a plus with minimum of 4-6 years of relevant experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in SAP, Veeva, and Cell Therapy operations strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding written and verbal written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Results oriented with the ability to demonstrate resiliency, ownership, and drive.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team oriented with excellent collaboration skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Must be able to work onsite daily and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed.\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$80,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$115,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4040012002,"name":"Technical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4036281002,"name":"Beam - NC","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8467816002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6382455002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8467816002,"updated_at":"2026-05-12T17:53:58-04:00","requisition_id":"517 - 2026 - 003","title":"Security and Network Operations Analyst","company_name":"Beam Therapeutics","first_published":"2026-03-18T10:23:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is looking for a highly motivated and detail-oriented Security and Network Operations Analyst to join our growing IT Team. This is a junior level position designed for candidates with 2-6 years of hands-on experience who are eager to learn and grow under the guidance of senior team members. The successful candidate will perform security assessments of Beam’s third-party partners, respond to security questionnaires from treatment centers and other external entities, support enterprise network infrastructure, cloud-managed networking, next-generation firewalls/SASE platforms, and managed detection \u0026amp;amp; response services. This position requires a minimum of two days per week on-site presence in our Cambridge, MA locations with an expectation that additional on-site days may be required to support the team and to provide response to incidents.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform internal and external security assessments\u0026amp;nbsp;working with vendors, internal teams, and treatment centers\u0026amp;nbsp;to support\u0026amp;nbsp;treatment\u0026amp;nbsp;center onboarding and\u0026amp;nbsp;Beam’s commercialization\u0026amp;nbsp;readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Beam’s procurement team to embed security reviews in the vendor onboarding process\u0026amp;nbsp;and establish a mechanism for periodic review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the regular review of\u0026amp;nbsp;internal\u0026amp;nbsp;security controls, ensuring compliance with established security standards such as NIST CSF 2.0\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the implementation and management of cloud-based solutions within Microsoft Azure\u0026amp;nbsp;and Amazon Web Services.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor network performance and security events, identifying and escalating issues to senior architects for resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initial triage of events and issues related to email security services and products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform routine network maintenance tasks such as firmware updates, patch management,\u0026amp;nbsp;and\u0026amp;nbsp;hardware troubleshooting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage SAML certificate rotation in MS Azure\u0026amp;nbsp;for deployed applications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage 3\u0026lt;sup\u0026gt;rd\u0026lt;/sup\u0026gt;\u0026amp;nbsp;party digital certificates (Digicert, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in incident response activities, analyzing security alerts and assisting in the containment and remediation of threats.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain documentation for network configurations, security policies, and troubleshooting\u0026amp;nbsp;guides.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Wi-Fi network deployments, including site surveys, configuration, and performance monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the configuration, deployment, and monitoring of network devices and services, including switches, routers, firewalls, and wireless access points.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with senior architects on projects involving network upgrades, new technology rollouts, and security enhancements.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help enforce security best practices across the organization, including vulnerability management and compliance with regulatory requirements.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in computer science\u0026amp;nbsp;or Certifications\u0026amp;nbsp;in\u0026amp;nbsp;information technology or cyber security, with\u0026amp;nbsp;2-6\u0026amp;nbsp;years of work experience.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience performing\u0026amp;nbsp;information security\u0026amp;nbsp;risk assessments.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Basic knowledge of networking concepts and protocols (TCP/IP, VLANs, VPNs).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of authentication models\u0026amp;nbsp;and identity providers (Azure, OKTA).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of fundamental information security principles and practices.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving skills and attention to detail.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work effectively in a team environment and communicate technical information clearly.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn and adapt to new technologies and procedures.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of the Cell and Gene Therapy industry or Biotechnology is a plus.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Candidates are expected to come onsite 1-3 days per week with an expectation that additional on-site days may be required to support the team and to provide response to incidents.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$80,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$115,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052072002,"name":"Information Technology","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8522675002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6404060002,"location":{"name":"Durham, NC"},"metadata":null,"id":8522675002,"updated_at":"2026-04-24T12:34:44-04:00","requisition_id":"331 - 2026 - 004","title":"Senior Manager, Quality Control Raw Materials","company_name":"Beam Therapeutics","first_published":"2026-04-24T09:51:21-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The QC Manager, Raw Materials will be responsible for developing, leading, and managing the Raw Materials QC program at the Beam Therapeutics Manufacturing facility in Durham, NC. This role will develop and maintain documentation regarding testing requirements and strategies, serve as a subject matter expert (SME) for raw materials issues, providing technical expertise aligned with current GMPs and current industry practices. This person will have knowledge and experience with USP methods, and the ability to apply as required, and as well as maintaining compliance to USP, ICH and FDA guidance documents. Interface with Manufacturing, Supply Chain, and Quality Assurance leadership and participate and/or lead interdepartmental teams to address quality-related issues.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role requires on-site presence and engagement. The position will report to the Quality Control Senior Director.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Primary Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and manage the raw materials QC program at the Beam Therapeutics Manufacturing facility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain all documentation with regards to testing requirements and strategies, including material specifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a SME for raw materials issues, providing technical expertise aligned with current GMPs and current industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage contract laboratories as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and author risk assessments for raw material programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support supplier change notifications and material enrollment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify need for development of new assays with compendial and GxP requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accountable for managing the raw materials testing program to ensure quality, product specifications and adherence to all current GMPs, USP, ICH and FDA guidance documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate QC systems and recommend and/or implement system improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author technical protocols and reports for Raw Materials testing qualification, validation, or verification.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author test methods and SOPs for the Raw Materials testing program.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create, review, and approve out-of-specification (OOS) and out-of-trend (OOT) investigations, deviations, CAPAs, and Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages release of raw materials used in manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight of material master data as it relates to inspection plans and material life cycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain records and databases in accordance with procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hire and manage staff as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee management of in-house raw material test equipment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s or advanced degree in biology, biochemistry or closely related scientific discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 7-10 years of CGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert knowledge of pharmaceutical/biotech Raw Materials testing is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 3 years of management experience is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Basic knowledge of qualifications and validations; current industry practices; and strong experience with guidance interpretation and application.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of cGMPs, ICH, USP, FDA requirements is required, including equipment and method validation/verification.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with risk assessment tools is desired\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent critical thinking and technical writing skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal and communication skills to lead, facilitate and follow.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Computer skills required to use Microsoft Word, Project, Visio, and Excel programs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$155,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$190,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052903002,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4036281002,"name":"Beam - NC","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8349934002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6334516002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8349934002,"updated_at":"2026-02-25T10:59:36-05:00","requisition_id":"219 - 2026 - 001","title":"Senior Manager, Statistical Programming","company_name":"Beam Therapeutics","first_published":"2025-12-22T10:26:54-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is looking for a highly talented and motivated Senior Manager, Statistical Programming, to join our growing Statistical Programming team in the Biometrics department. The senior manager will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure successful execution for Beam’s clinical programs. In this role, you will work with the lead of statistical programming to develop statistical programming strategies and timelines. You will manage CROs, oversee programming activities and provide timely support to the cross-functional teams on statistical programming matters according to the project strategies and requests.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Participates in statistical programming activities on clinical studies and oversees CROs to generate analysis data sets and tables, listings and figures needed for clinical study reports and regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reviews and validates SDTM, ADaM analysis datasets and TFLs created by CROs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works collaboratively and communicates effectively with Biostatistics, Data Management, clinical operations, clinical development, Regulatory and other functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages creating CDSIC SDTM and ADaM datasets, analysis metadata results and Define.xml for Electronic Submission from the clinical database or external data sources.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages the activities of data summary, statistical analysis, patient profile, safety and efficacy tables, listings and figures using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS and R.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates and manages the workflow of generating study specific and ad-hoc clinical data listings, summary tables and figures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partners with Statisticians and other members of the clinical study team, performs ad hoc analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reviews SAP, DMP, CRF, annotated CRF, table shells and other relevant documents by CROs and provides expert feedback from functional perspective.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops SAS programming infrastructure and programming processes improve data deliverables and ad hoc analyses quality and efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Builds and mentors a team of programmers as needed to support Beam clinical trials and development pipelines.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MS or higher degree in Statistics, Mathematics, or related scientific Discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 10 years Pharmaceutical/Biotech programming experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced SAS programming skills and strong Statistical background along with experience with SAS Base, SAS/Macros, SAS/Graph and SAS/Stat.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience and in-depth knowledge in CDISC including STDM, ADaM and controlled terminologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;NDA or BLA submission experience is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills and ability to prioritize tasks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing CROs and other data vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of ICH guidelines, Good Clinical Practices, FDA / EMA / other regulatory authority guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with R-Shiny is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;#LI-Hybrid\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$155,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$190,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4071033002,"name":"Biometrics","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8466467002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6381943002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8466467002,"updated_at":"2026-04-29T15:41:28-04:00","requisition_id":"334 - 2026 - 002","title":"Senior Manager, Supply Planning","company_name":"Beam Therapeutics","first_published":"2026-03-17T14:25:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is seeking a highly motivated individual to join our Supply Chain team. The Supply Planning \u0026amp;amp; Network leader will be responsible managing the global supply network performance by conducting risk-based inventory reviews and developing strategic options to address demand uncertainties and enhance network capabilities. He/she will be accountable to ensure uninterrupted supply of clinical and future commercial products via Beam’s S\u0026amp;amp;OP process. This role will report to the Sr. Director of Global Supply Chain Planning and partner with TechOps, Clinical Ops, Commercial Patient Ops, Quality, Finance, and CMC teams to lead short-term integrated production planning and long-range strategic supply chain planning of Beam’s product portfolio. The role will be responsible for leading a global inventory management program to ensure critical material availability at Beam NC \u0026amp;amp; CDMO mfg sites. The role will be integral to enhancing site planning and scheduling capabilities at Beam’s mfg site in Durham, NC and partnering with SAP business lead on further advancing technology capabilities. The ideal candidate will have a demonstrated track record of leading in a dynamic environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross functional relationships.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Production \u0026amp;amp; Capacity Planning: Develop and maintain a rolling 12–24-month master production schedule (MPS) aligned with demand forecasts and manufacturing constraints.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;External Network Collaboration: Lead planning and partner with key stakeholders to ensure supply continuity across the Contract Manufacturing Organizations (CMOs) and 3PLs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sales \u0026amp;amp; Operations Planning (S\u0026amp;amp;OP): Drive the monthly S\u0026amp;amp;OP cycle, including rough-cut capacity planning and scenario analysis. Partner cross-functionally to refine demand forecasts and execute supply network analysis to support both tactical and strategic goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Inventory Optimization: Ensures appropriate inventory levels to minimize excess while preventing stockouts, specifically managing shelf-life/expiry for temperature-sensitive products like Critical Materials (pDNA, mRNA, gRNA, mAb, lipids), Drug Substance, and Bulk/Finished Drug Product.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical/Launch Readiness: Orchestrate supply for clinical trials or support new product introductions (NPI) and commercial launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Risk Management: Proactively identify supply disruptions and develop mitigation strategies or business continuity plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process Improvement: Drive Global Supply Chain excellence through project management, process enhancement, and the deployment of digital tools that streamline business execution and strategic decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Metrics: Leverage data-driven KPIs to track performance, ensuring accountability and optimizing the balance between operational efficiency and financial health.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Systems: Optimize supply and inventory planning accuracy through utilization of SAP, driving improved stock maintenance and network visibility. Spearhead the design and execution of SAP enhancements, including Integrated Business Planning (IBP) and Jurisdictional Control (JC), to streamline end-to-end supply chain functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA degree in Business, Science, Engineering or related field with 8-10+ years of experience in global supply chain from pharma, biotech or cell \u0026amp;amp; gene therapy companies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Master\u0026#39;s degree or MBA preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior drug development, manufacturing, and clinical operations experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Final title/scope of role will be commensurate with experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Passion for patients, collaborative and effective leader.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of practical implications of Sarbanes-Oxley controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of continuous improvement methodologies and tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and facilitation skills, with high degree of customer focus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise and track record in manufacturing and supply chain execution and oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in supply chain planning, SAP ERP system, capacity modeling, supply network strategy and optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise and have a proven track record in supply chain risk management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid knowledge of regulatory requirements, regulatory guidance, including pharmaceutical GMPs and ICH guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current on Biopharma supply chain, manufacturing technologies, supplier network, CMO network, performance and capacity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possesses understanding and application of principles, concepts, practices, and standards for DS and DP manufacturing in the biopharma industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, negotiation, and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical skills and ability to clearly communicate at tactical and strategic level with team and Sr Management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a dynamic and challenging environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Some travel may be required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work onsite, not a remote role.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$155,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$190,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4076374002,"name":"Supply Chain","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8350466002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6334722002,"location":{"name":"Houston/Dallas"},"metadata":null,"id":8350466002,"updated_at":"2026-05-13T14:47:14-04:00","requisition_id":"251 - 2026 - 011","title":"Senior Medical Science  Liaison/Medical Science Liaison – South Central Region","company_name":"Beam Therapeutics","first_published":"2025-12-22T14:05:47-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are building a best‑in‑class Field Medical organization as a natural next step in the growth of our Medical Affairs organization at Beam therapeutics! This Director (or Associate Director) level MSL will own a defined US territory with primary responsibility in sickle cell disease (SCD) and shared accountability across the Beam pipeline, including Alpha‑1 antitrypsin deficiency (Alpha‑1) and glycogen storage disease 1a (GSD). You will architect territory strategy, onboard priority treatment centers, engage KOLs and HCPs, generate actionable insights, and drive pre‑commercial launch readiness in close collaboration with cross‑functional partners.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups; prioritize accounts and set measurable objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements; partner with internal teams for qualification and activation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform; foster advocacy and awareness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value \u0026amp;amp; Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally with Commercial, Market Access, and Clinical teams while preserving medical independence; coordinate account plans to ensure seamless patient access and avoid duplication.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent the company at congresses and external scientific meetings: plan and execute presence, engage in meaningful scientific exchanges, and follow up to strengthen visibility and credibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide education and resources to treatment centers on operational readiness for advanced therapies, including apheresis and cell-handling processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a trusted resource for compliance and ethical standards: ensure all interactions and materials meet company policies, regulatory requirements, and industry codes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain operational excellence: document activities and insights in CRM, monitor KPIs, and continuously improve processes, content, and tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and deliver training for internal teams and external stakeholders on rare disease management and CGT fundamentals to support launch readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a scientific ambassador for the company: articulate the value of the platform and pipeline to diverse audiences including clinicians, researchers, and advocacy groups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor evolving evidence and competitive landscape in rare disease and CGT; share updates internally to inform strategy and decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced scientific degree (PharmD, PhD, MD, or equivalent).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;~10+ years industry experience in Medical Affairs with significant Field Medical tenure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rare disease expertise required; hematology strongly preferred with emphasis on SCD.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Small biotech experience preferred; demonstrated impact in resource‑constrained settings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independent, proactive operator with strong ownership;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills; ability to translate complex science into clear, credible narratives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical strength for insight collection, synthesis, and actionable recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel up to ~60% across assigned territory.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;#LI-Remote\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$185,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$225,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4099201002,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4098424002,"name":"Beam - Field","location":null,"child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8350451002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6334717002,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":8350451002,"updated_at":"2026-04-28T14:26:34-04:00","requisition_id":"251 - 2026 - 010","title":"Senior Medical Science  Liaison/Medical Science Liaison – Southwest Region","company_name":"Beam Therapeutics","first_published":"2025-12-22T13:58:40-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are building a best‑in‑class Field Medical organization as a natural next step in the growth of our Medical Affairs organization at Beam therapeutics! This Director (or Associate Director) level MSL will own a defined US territory with primary responsibility in sickle cell disease (SCD) and shared accountability across the Beam pipeline, including Alpha‑1 antitrypsin deficiency (Alpha‑1) and glycogen storage disease 1a (GSD). You will architect territory strategy, onboard priority treatment centers, engage KOLs and HCPs, generate actionable insights, and drive pre‑commercial launch readiness in close collaboration with cross‑functional partners.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups; prioritize accounts and set measurable objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements; partner with internal teams for qualification and activation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform; foster advocacy and awareness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value \u0026amp;amp; Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally with Commercial, Market Access, and Clinical teams while preserving medical independence; coordinate account plans to ensure seamless patient access and avoid duplication.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent the company at congresses and external scientific meetings: plan and execute presence, engage in meaningful scientific exchanges, and follow up to strengthen visibility and credibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide education and resources to treatment centers on operational readiness for advanced therapies, including apheresis and cell-handling processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a trusted resource for compliance and ethical standards: ensure all interactions and materials meet company policies, regulatory requirements, and industry codes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain operational excellence: document activities and insights in CRM, monitor KPIs, and continuously improve processes, content, and tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and deliver training for internal teams and external stakeholders on rare disease management and CGT fundamentals to support launch readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a scientific ambassador for the company: articulate the value of the platform and pipeline to diverse audiences including clinicians, researchers, and advocacy groups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor evolving evidence and competitive landscape in rare disease and CGT; share updates internally to inform strategy and decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced scientific degree (PharmD, PhD, MD, or equivalent).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;~10+ years industry experience in Medical Affairs with significant Field Medical tenure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rare disease expertise required; hematology strongly preferred with emphasis on SCD.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Small biotech experience preferred; demonstrated impact in resource‑constrained settings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independent, proactive operator with strong ownership;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills; ability to translate complex science into clear, credible narratives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analytical strength for insight collection, synthesis, and actionable recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel up to ~60% across assigned territory.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;#LI-Remote\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$185,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$225,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4099201002,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4098424002,"name":"Beam - Field","location":null,"child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8522656002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6404055002,"location":{"name":"Durham. NC"},"metadata":null,"id":8522656002,"updated_at":"2026-05-28T15:58:22-04:00","requisition_id":"522 - 2026 - 001","title":"Senior Technician, Instrumentation and Calibration","company_name":"Beam Therapeutics","first_published":"2026-04-24T10:08:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Facility Technician, Instrumentation and Calibration is a multi-disciplinary role whose primary focus will be performing calibrations on Facility, Utility, lab, and Process Equipment to include management of standards and optimization of maintenance and calibration procedures. In addition to this primary responsibility, secondary responsibilities include supporting the overall maintenance of Facility and Utility Equipment by completing maintenance activities outside of calibrations; additionally, this role will support the 24x7 support strategy by being apart of the “on call” program. In addition to a varied general maintenance background, the ideal candidate should also possess the ability to work with personnel from Quality, Validation, Laboratories, IT, Finance, and Administration.\u0026amp;nbsp; This is a M-F Day Shift Position subject to after hour and weekend support.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience with performing calibrations on Utility, Lab, and Process Equipment. Examples include: pressure, flow, velocity, temperature, pH, conductivity, weight, time, gas systems, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with the management of instrument standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive change and champion continuous improvements by improving calibration procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute planned and demand maintenance activities for plant utilities (HVAC, Electrical, Chilled/Heating Hot Water, Compressed Air), gene therapy manufacturing equipment, and QC laboratory instrumentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support CapEx and Process Improvement project initiatives as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and schedule vendors for maintenance and calibration tasks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond and remediate alarms from the Building Automation and Process Control systems and site equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create individual work and review vendor work within the site CMMS system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliant operations in accordance with site cGMP, environmental, and government requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to participate in on-call rotation with members of the Facility Maintenance team.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Post-secondary degree, certification(s), or equivalent experience in a technical discipline related to MEP, construction, utilities, or trades. Supervisory experience with technicians \u0026amp;amp;/or vendors preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8-10 years’ experience in calibration and maintenance with a preference for biotech, pharma, or medical device manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of process equipment, utility systems, and lab equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Computer systems literacy, with Siemens BAS, DeltaV, and CMMS experience required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage competing priorities and timelines and adapt quickly to changing circumstances.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible and results oriented, with a focus on excellent customer service and demonstrated collaboration in a team environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Must be able to work onsite daily and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed. \u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Hourly Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$50\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$70 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4093961002,"name":"Facilities","child_ids":[],"parent_id":null}],"offices":[{"id":4036281002,"name":"Beam - NC","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545655002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413355002,"location":{"name":"Durham, NC"},"metadata":null,"id":8545655002,"updated_at":"2026-06-08T11:00:05-04:00","requisition_id":"331 - 2026 - 006","title":"Specialist II, Product Quality Assurance","company_name":"Beam Therapeutics","first_published":"2026-05-12T11:37:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Specialist II, NC Product Quality Assurance (PQA) will be responsible for supporting Quality\u0026#39;s oversight of laboratory and manufacturing operations at Beam\u0026#39;s manufacturing facility in RTP, North Carolina. The NC manufacturing facility is focused on advanced therapeutic manufacturing technologies (cell and gene therapy modalities). The facility is currently focused on clinical phase manufacturing with the intent of moving several programs to be commercial within the same facility.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The role will provide Quality oversight of routine manufacturing, testing, and related operations to ensure that systems and processes are maintained in compliance with Good Manufacturing Practices (GMP), and ultimately to Good Distribution Practices (GDP) as the programs move to the commercial phase. This role will also provide Manufacturing Shop Floor Quality presence and may require support on first or second shift as required by plant scheduling.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The responsibilities include batch record review, logbook review, asset inductions and work order approvals, approval and management of associated Deviations/CAPAs, and support of product disposition activities. The position will report into Beam NC, Director of PQA.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Specialist II, NC PQA is expected to be an on-site resource, with alternate shift schedule, for project start-up and routine clinical and commercial operations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Primary Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide Quality oversight of on-the-floor activities including manufacturing shop floor presence during operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Quality oversight of QC testing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for ensuring GMP compliance with applicable procedures and production requirements in QC, manufacturing, and facilities operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for assisting with product disposition activities of supply produced at the manufacturing facility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Real time review of batch records and labels.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approval of manufacturing discrepancies and associated CAPA’s.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicating lot disposition pending issues to management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Aid in the development and ongoing improvement of applicable quality systems for the site; identifying gaps or improvements, authoring and approval of procedures, and providing training, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve calibration and maintenance work orders and asset inductions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support approval of protocols when required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support tech transfers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support commissioning, qualification, and validation of equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Quality support towards resolution of material, product, environmental, facility and equipment manufacturing issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for supporting functional and facility goals and objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for supporting and contributing to quality metrics for the facility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for supporting and participating in regulatory inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for communication and escalation of significant issues that may impact patient safety, product quality, supply, regulatory compliance, or company impact to senior management.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelors or Advanced degree in a scientific discipline with 3-4 years’ experience in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and/or quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of aseptic processing, and/or cell and gene therapy is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Apply Quality concepts and company policies to resolve issues of moderate complexity in an effective manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills, detail-oriented personality, and ability to work collaboratively across functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of global regulations and standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong team player that has a customer service approach and is solution oriented.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and the ability to work individually as well as within a multi-disciplinary team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent listening, communication and interpersonal skills with a team focus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Consistent delivery of high-quality work.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to gown and work in a cleanroom environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Must be able to work onsite daily\u0026lt;/strong\u0026gt; and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$105,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4052903002,"name":"Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4036281002,"name":"Beam - NC","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/6305863002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":null,"location":{"name":"Cambridge, MA and Durham, NC"},"metadata":null,"id":6305863002,"updated_at":"2026-02-02T10:40:26-05:00","requisition_id":null,"title":"Submit your resume for future full time openings","company_name":"Beam Therapeutics","first_published":"2022-08-03T15:15:54-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Not seeing a role that suits you?\u0026amp;nbsp; Send us your resume and we will keep you in mind for future opportunities on the Beam Team!\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4073122002,"name":"Future Openings","child_ids":[],"parent_id":null}],"offices":[]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/6440268002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":null,"location":{"name":"Durham, NC"},"metadata":null,"id":6440268002,"updated_at":"2026-02-02T10:23:13-05:00","requisition_id":null,"title":"Submit your resume for future Manufacturing and Quality roles located in RTP, NC","company_name":"Beam Therapeutics","first_published":"2022-10-14T13:47:28-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Beam is preparing to open a state-of-the-art Manufacturing facility located on Davis Drive in RTP, NC and will be looking for Manufacturing and Quality professionals to join our team!\u0026amp;nbsp; Please submit your resume here to be considered for positions that we will be opening in Q4 2022 and throughout 2023.\u0026amp;nbsp; We are looking for fearless innovators who are passionate about helping patients and looking to join a collaborative environment where you will be able to have a direct impact on getting our facility up and running.\u0026amp;nbsp;\u0026lt;/p\u0026gt;","departments":[{"id":4075080002,"name":"Future RTP North Carolina Openings","child_ids":[],"parent_id":null}],"offices":[]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8392998002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6350824002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8392998002,"updated_at":"2026-04-29T10:41:59-04:00","requisition_id":"519 - 2026 - 002","title":"Vice President, Compliance","company_name":"Beam Therapeutics","first_published":"2026-01-27T13:41:20-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Vice President, Compliance is a strategic leader responsible for designing, implementing, and continuously improving the company’s Corporate Compliance Program to oversee promotional materials, field training, and HCP/patient programs. As an objective advisor, the Vice President, Compliance ensures the organization operates with integrity and in compliance with all applicable laws, regulations, and internal policies. Reporting to the Chief Legal Officer, the Vice President, Compliance partners with executive leadership, the legal and compliance function, the Audit Committee of the Board of Directors, and employees at all levels to foster a culture of ethical conduct and accountability.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is transitioning to a commercial stage company, and this position plays a critical role in developing a culture of compliance.\u0026amp;nbsp; Additionally, ex vivo cell therapy and in vivo gene therapy have unique commercial and operational needs that require a strategic leader to collaborate with commercial, medical, and manufacturing to build a commercial process that delivers for patients compliantly.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop, execute, and evolve a comprehensive compliance strategy and program focusing on healthcare compliance and aligning with business objectives and legal requirements that meets the unique needs of cell and gene therapy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide proactive strategic advice to the business to help drive commercial success and ensure compliance with applicable laws and company policies, including federal and state anti-kickback and false claims laws; U.S. and other country anticorruption laws; the federal Food, Drug and Cosmetic Act; and federal and state transparency laws.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as Chair of the Beam Compliance Committee and as Data Privacy Officer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide regular updates on the Compliance Program to executive leadership and the Audit Committee of the Board of Directors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review business strategy plans and business development opportunities for compliance risks and advise the business on how to mitigate those risks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain trusting relationships with key client groups, such as commercial and clinical, and serve as a trusted and strategic advisor and resource.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a compliance champion to reinforce a culture of integrity and raise awareness of compliance as a collective responsibility of all company personnel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion open communication by ensuring employees feel empowered to raise concerns without fear of retaliation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee ongoing education initiatives to enhance understanding of the Code of Business Conduct \u0026amp;amp; Ethics, Beam policies and procedures, and emerging compliance risks, and seeking opportunities for continuous learning across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuously assess the effectiveness of the compliance program through data-driven audits, risk assessments, and performance metrics. Identify gaps and support the design and tracking of corrective actions to strengthen compliance controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and conduct compliance investigations, working with internal business partners to identify appropriate corrective and preventive actions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay ahead of regulatory and industry code changes and industry and enforcement trends impacting compliance areas and proactively advise leadership on potential impacts and necessary adaptations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a trusted advisor to the Board of Directors, Chief Legal Officer, executive leadership team, and other functions, providing actionable guidance on compliance matters and risk mitigation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage with outside counsel, regulatory agencies, and industry groups to understand and benchmark the best practices and ensure the compliance regime meets or exceeds industry standards.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required, Juris Doctorate or advanced degree a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cell and gene therapy experience a must.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relevant experience (typically 7 years or more, or equivalent combination of education, training, and experience) with a deep understanding of compliance issues confronting the pharmaceutical/biotech industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated knowledge and understanding of the requirements for effective compliance programs as set forth in the OIG Compliance Program Guidance for Pharmaceutical Manufacturers and the U.S. Sentencing Guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated effectiveness operating in complex organizational and regulatory environments and experience with Code implementation (PhRMA, EFPIA, IFPMA)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated knowledge and understanding of the legal and regulatory framework affecting the pharmaceutical industry including sales and marketing, OIG and other industry guidance documents, regulations on the promotion of marketed products, clinical trial regulations, patient privacy and issues arising under the False Claims Act, anti-bribery/anti-corruption laws, and other related laws.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Business focused and solution oriented.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written, oral and presentation skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to work with all levels of management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong problem-solving and analytical skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated and able to perform role independently, with a minimum level of supervision.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to partner effectively with others in addressing complex issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong influencing skills and sound business judgment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to appropriately prioritize issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$310,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$400,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4040007002,"name":"Legal","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]},{"absolute_url":"https://job-boards.greenhouse.io/beamtherapeutics/jobs/8545751002","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":6413392002,"location":{"name":"Cambridge, MA"},"metadata":null,"id":8545751002,"updated_at":"2026-05-14T15:10:09-04:00","requisition_id":"251 - 2026 - 014","title":"Vice President, Global RWE and HEOR Strategy","company_name":"Beam Therapeutics","first_published":"2026-05-14T15:08:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Company Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beam is seeking a dynamic, visionary, and strategic \u0026lt;strong\u0026gt;Vice President,\u0026lt;/strong\u0026gt; \u0026lt;strong\u0026gt;Global RWE and HEOR Strategy\u0026lt;/strong\u0026gt; to spearhead the global HEOR strategy for our sickle cell disease program (risto-cel) and other pipeline programs as they emerge.\u0026amp;nbsp; Sitting within the Medical Affairs function, in this high-impact role, the \u0026lt;strong\u0026gt;Vice President,\u0026lt;/strong\u0026gt; \u0026lt;strong\u0026gt;Global RWE and HEOR Strategy\u0026lt;/strong\u0026gt; will develop and execute evidence-generation plans, manage stakeholder relationships, and shape external communication strategies. You will partner closely with Clinical Development, Medical Communications and Scientific Publications, Value and Evidence Strategy, Commercial, R\u0026amp;amp;D, and additional cross-functional teams. If you thrive in a collaborative, mission-driven environment and are eager to shape the future of sickle cell disease care, we want you to bring your expertise and passion to Beam.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic input to disease prioritization, target product profiles, clinical trial protocols, clinical development plans, and regulatory submissions; lead development of clinical sections for Investigator’s Brochures, briefing books, safety updates, IND/NDA materials, and responses to Health Authority questions.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, validate, and integrate patient‑centered outcomes (PROs) into protocols and analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interpret clinical trial results (including PROs and healthcare resource use) and partner with Clinical Development/Biostatistics on Statistical Analysis Plans (SAPs) and post‑hoc analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead a fit‑for‑purpose RWE strategy (EHR, claims, registries, hybrid/open datasets) including natural history/registry design and governance to inform endpoints, recruitment, and post‑authorization effectiveness/safety assessments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and operationalize external/synthetic control arm approaches (e.g., matched registry cohorts, Bayesian borrowing) for single‑arm or small‑population studies typical in cell \u0026amp;amp; gene therapy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide operational oversight of Medical Affairs evidence generation, including vendor/CRO governance, milestone/deliverable tracking, data‑quality plans, risk management, and on‑time execution across Medical Affairs–led studies; contribute to long‑term capability building (digital health, real‑world studies).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Elicit and integrate perspectives from patients, KOLs, policy leaders, and internal stakeholders (market access, marketing, patient advocacy) to ensure plans meet the needs of patients, HCPs, and payers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Market Access on internal and external payer/policy initiatives (pricing and reimbursement, unmet medical need, regional market dynamics, evidence gaps) across the portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support business decisions around ex-US strategy including, but not limited to, scoping ex-US opportunities, prioritizing country engagement, early scientific advice / parallel consultations with EMA and HTA bodies (e.g., HTACG/JSC),\u0026amp;nbsp;providing advice to development programs on endpoint selection to support\u0026amp;nbsp;product and reimbursement approvals ex-US,\u0026amp;nbsp;etc.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipate payer evidence needs and budget‑impact critiques\u0026amp;nbsp;(including preparation for ICER Reviews).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and\u0026amp;nbsp;maintain\u0026amp;nbsp;economic models (cost‑effectiveness, budget impact) tailored to one‑time CGTs, addressing uncertainty/durability and caregiver burden.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Market Access to\u0026amp;nbsp;design innovative payment models and outcomes‑based agreements with pragmatic outcomes and tracking.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the AMCP dossier and pre‑approval information exchange (PIE) strategy (6–12\u0026amp;nbsp;months pre‑launch).\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work collaboratively with internal teams, consultants, and CROs to advance development of the portfolio.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Master’s Degree or higher in Health Economics and Outcomes Research or a relevant discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Formal training in Epidemiology/Health Services Research required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;20+ years’ experience in observational research study management AND data analytics, either within industry or with an observational research consulting firm.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record in drug development, with rare disease experience and an existing network of hematologists preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead in a matrixed, cross-functional environment, combining strategic agility with strong business acumen.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Independent, proactive operator with strong ownership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cross functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, collaboration, and problem-solving skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Onsite requirements: Candidates are expected to come onsite 1-3 days per week.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;description\u0026quot;\u0026gt;\u0026lt;p\u0026gt;The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Beam Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$310,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$400,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4099201002,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4040843002,"name":"Beam - Cambridge","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":4021353002}]}],"meta":{"total":26}}