{"jobs":[{"absolute_url":"https://elevate.bio/about/jobs/6005993004?gh_jid=6005993004","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":5158746004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6005993004,"updated_at":"2026-06-12T13:40:52-04:00","requisition_id":"P100793","title":"Associate I, QC Microbiology (Contract)","company_name":"ElevateBio","first_published":"2026-05-28T14:12:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate I, QC Microbiology is responsible for performing routine activities at our Waltham facility. This role will be responsible for ensuring daily functions and responsibilities of the QC Microbiology group within the laboratory and clean rooms are completed accurately and efficiently. Activities of this position include but are not limited to, laboratory assays, environmental monitoring activities, data entry, and review.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine environmental monitoring, utility monitoring, and safety testing of Cell Therapy drug products, ensuring that all work is carried out per cGMPs and applicable policies and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform standard QC Microbiological assays.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bioburden, Endotoxin, Sterility, Growth Promotion, TOC/Conductivity, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Peer-reviewing assay results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performing routine Data Entry/Review with LIMS systems.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform routine QC Microbiology Environmental Monitoring and Utility Monitoring testing in Grade A/B/C and D cleanrooms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform routine Preventative Maintenance (PMs) for QCM Equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Quality Events including: Laboratory Investigations, Deviations, CAPA’s, Change Controls and associated Quality Actions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with 0-2 years of experience in a GMP Quality Control microbiology lab setting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate and work collaboratively cross departmentally and within a team, as well as being able to complete tasks independently for routine tasks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent Organizational skills and attention to detail is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to follow and execute SOP’s.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Skills \u0026amp;amp; Competencies: \u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of GMP, GLP, SOPs, and quality system processes a plus.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Environmental monitoring as it applies to USP/ISO/EU Regulations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in Cell and Gene Therapy manufacturing environment is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with MODA, Veeva, Kneat, SAP, and BMRAM is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Work Environment \u0026amp;amp; Physical Demands:\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Able to lift and carry 20 lbs (equipment/materials)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to be on feet for 4 hours at a time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to Aseptically Gown\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to support Off-Shift Hours for Product testing\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is\u0026lt;strong\u0026gt; $33/hour - $48/hour\u0026lt;/strong\u0026gt;. This range is a good faith estimate of the expected \u0026lt;strong\u0026gt;hourly\u0026lt;/strong\u0026gt;\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025605004,"name":"Quality Control","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6010595004?gh_jid=6010595004","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":5160841004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6010595004,"updated_at":"2026-06-02T13:17:56-04:00","requisition_id":"P100797","title":"Biomanufacturing Associate I (Contract)","company_name":"ElevateBio","first_published":"2026-06-02T13:17:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, TILs, and mRNA. The individual should be a motivated self-starter eager to contribute to supporting a manufacturing organization unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform manufacturing activities including but not limited to reviewing / authoring SOPs and batch records, as well as material ordering / management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input for the selection and set-up of equipment, process, and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Quality Assurance and MSAT to proactively resolve issues such as deviations, CAPAs, Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process development, facilities \u0026amp;amp; engineering, MSAT, quality control, and quality assurance to ensure right-first-time manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and review batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in safety, quality, delivery and cost\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with 0-2 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some of the following is preferred: cGMP manufacture and/or process development for CAR T, TCR, TIL, cell and gene therapies, and mRNA.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of primary cell culture and experience with equipment such as BSC, Microscope, LOVO, CliniMACS, Incubators, Centrifuges, CRF, and G-Rex systems is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic technique and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Rotating 12-hour day shifts (0700-1900).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available to overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, stretch for extended periods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;$33/hour - $48/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6011555004?gh_jid=6011555004","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":5161280004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6011555004,"updated_at":"2026-06-03T16:02:15-04:00","requisition_id":"P100800","title":"Biomanufacturing Associate I (Contract)","company_name":"ElevateBio","first_published":"2026-06-03T16:02:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AVV) and Lentivirus (LV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform manufacturing/operations start-up activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input on teams for the selection and set-up of equipment, process, and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process sciences, development, facilities \u0026amp;amp; engineering, tech ops, quality control, quality assurance, to ensure right-first-time technology transfer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in process, safety, quality, and cost\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with 0-2 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some of the following is preferred: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic technique and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;12-hour Rotating Shift.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available to overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, stretch for extended periods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $33 - $48. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6010447004?gh_jid=6010447004","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":5160787004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6010447004,"updated_at":"2026-06-02T13:17:27-04:00","requisition_id":"P100795","title":"Biomanufacturing Associate I (Contract)","company_name":"ElevateBio","first_published":"2026-06-02T13:17:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AVV) and Lentivirus (LV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform manufacturing/operations start-up activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input on teams for the selection and set-up of equipment, process, and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process sciences, development, facilities \u0026amp;amp; engineering, tech ops, quality control, quality assurance, to ensure right-first-time technology transfer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in process, safety, quality, and cost\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with 0-2 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some of the following is preferred: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic technique and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;7 Day 12-hour Rotating shifts (7am-7pm)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available to work overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, stretch for extended periods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;$33/hour - $48/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6030555004?gh_jid=6030555004","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":5172543004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6030555004,"updated_at":"2026-06-16T15:43:11-04:00","requisition_id":"P100813","title":"Biomanufacturing Associate II","company_name":"ElevateBio","first_published":"2026-06-16T15:43:11-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, TILs, and mRNA. The individual should be a motivated self-starter eager to contribute to supporting a manufacturing organization unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform manufacturing activities including but not limited to reviewing / authoring SOPs and batch records, as well as material ordering / management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input for the selection and set-up of equipment, process, and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Quality Assurance and MSAT to proactively resolve issues such as deviations, CAPAs, and Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process development, facilities \u0026amp;amp; engineering, MSAT, quality control, and quality assurance to ensure right-first-time manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in the service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and review batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in safety, quality, delivery and cost\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with 2-4 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some of the following is preferred: cGMP manufacture and/or process development for CAR T, TCR, TIL, cell and gene therapies, and mRNA.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of primary cell culture and experience with equipment such as BSC, Microscope, LOVO, CliniMACS, Incubators, Centrifuges, CRF, and G-Rex systems is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic techniques and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in a dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Monday – Friday 0800-1600 with the ability to flex schedule.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, stretch for extended periods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, and holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $38/hour - $52/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6021070004?gh_jid=6021070004","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":5165857004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Employee","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Regular","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6021070004,"updated_at":"2026-06-15T10:21:49-04:00","requisition_id":"P100811","title":"Biomanufacturing Associate II ","company_name":"ElevateBio","first_published":"2026-06-12T13:49:54-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, TILs, and mRNA. The individual should be a motivated self-starter eager to contribute to supporting a manufacturing organization unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform manufacturing activities including but not limited to reviewing / authoring SOPs and batch records, as well as material ordering / management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input for the selection and set-up of equipment, process, and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Quality Assurance and MSAT to proactively resolve issues such as deviations, CAPAs, Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process development, facilities \u0026amp;amp; engineering, MSAT, quality control, and quality assurance to ensure right-first-time manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and review batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in safety, quality, delivery and cost\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with 2-4 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some of the following is preferred: cGMP manufacture and/or process development for CAR T, TCR, TIL, cell and gene therapies, and mRNA.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of primary cell culture and experience with equipment such as BSC, Microscope, LOVO, CliniMACS, Incubators, Centrifuges, CRF, and G-Rex systems is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic technique and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Rotating 12-hour day shifts (0700-1900).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available to overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, stretch for extended periods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $38/hour - $52/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6010448004?gh_jid=6010448004","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":5160788004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6010448004,"updated_at":"2026-06-02T11:31:59-04:00","requisition_id":"P100796","title":"Biomanufacturing Associate II (Contract)","company_name":"ElevateBio","first_published":"2026-06-02T11:31:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AVV) and Lentivirus (LV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform and lead routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform manufacturing/operations start-up activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide training to team on set-up and use of equipment, process and material flows, as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure clean rooms are maintained in an organized and ready state.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process sciences, development, facilities \u0026amp;amp; engineering, tech ops, quality control, quality assurance, to ensure right-first-time technology transfer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closing with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in process, safety, quality, and cost\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with at least 2 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some of the following is preferred: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic technique and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Rotating 7 Day 12-hour shifts. (7am-7pm)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available to work overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, stretch for extended periods\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;$38/hour - $52/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6030556004?gh_jid=6030556004","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":5172544004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6030556004,"updated_at":"2026-06-16T15:33:49-04:00","requisition_id":"P100815","title":"Biomanufacturing Associate II (Contract)","company_name":"ElevateBio","first_published":"2026-06-16T15:21:06-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AVV) and Lentivirus (LV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform and lead routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform manufacturing/operations start-up activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide training to team on set-up and use of equipment, process and material flows, as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure cleanrooms are maintained in an organized and ready state.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process sciences, development, facilities \u0026amp;amp; engineering, tech ops, quality control, quality assurance, to ensure right-first-time technology transfer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closing with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in process, safety, quality, and cost\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with:\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;For BMA II’s, 2-3+  years of experience in cGMP biotech manufacturing, preferably cell and gene therapies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of experience in project leadership is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some or all of the following: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic technique and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8-hour day shifts, Monday through Friday\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available to overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, and stretch for extended periods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $38/hour - $52/hour. This range is a good faith estimate of the expected\u0026amp;nbsp;hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6017345004?gh_jid=6017345004","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":5163987004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Employee","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Regular","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6017345004,"updated_at":"2026-06-10T14:29:54-04:00","requisition_id":"P100806","title":"Director, Quality Systems \u0026 Compliance","company_name":"ElevateBio","first_published":"2026-06-10T14:29:54-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;The Role:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director, Quality Systems and Compliance provides strategic direction and oversight of Quality Systems, Compliance, and Business System Ownership to ensure execution meets regulatory requirements, industry best practices, and modern digital, data-driven expectations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is accountable for evolving the Quality Management System (QMS) into a digitally enabled, scalable, and continuously improving ecosystem supporting clinical through commercial operations. The incumbent serves as a senior Digital System Owner leader, transforming Quality Systems into intelligent, data-driven platforms that enhance compliance, improve operational performance, and enable decision-making.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is a critical influencer across the organization, driving adoption and effective use of Quality Systems and ensuring they deliver measurable business value. Success requires leadership beyond traditional system management—delivering value from systems by translating compliance requirements into efficient, practical, and scalable solutions that enable the business to operate effectively and transparently while maintaining a strong compliance posture.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Here’s What You’ll Do:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Quality Systems Leadership\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and continuously improve Quality Systems, including Document Management, Training, CAPA, Deviations, Change Control, Risk Management, Supplier Quality, and Audit/Inspection Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and drive the program for continuous inspection readiness, ensuring sustained audit preparedness through proactive monitoring, internal audits, and system effectiveness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary host and lead for client audits, including preparation, on-site execution, stakeholder coordination, and audit response strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead regulatory inspections and client audits, ensuring effective preparation, execution, and follow-up\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the Quality Management Review (QMR) process, monitoring system health, identifying trends and risks, and driving continuous system and process improvements\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Digital System Ownership \u0026amp;amp; AI Enablement\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as Business System Owner for eQMS, DMS, and LMS, accountable for system strategy, lifecycle, performance, and adoption\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive optimization through automation, advanced analytics, and native AI capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement AI-enabled use cases such as:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Predictive quality signal detection and trending\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deviation and CAPA pattern recognition\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Automated reviews, compliance checks, and standardization of quality processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Intelligent workflow routing and prioritization\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure systems remain validated and compliant with Part 11, Annex 11, and CSA expectations, while improving operational efficiency\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality System Adoption \u0026amp;amp; Value Realization\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as a primary influencer for enterprise-wide adoption and effective use of Quality Systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure systems are user-centric, efficient, and enable improved execution of quality processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate regulatory requirements into solutions that improve efficiency and support business objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with functional leaders to enable transparent, compliant, and effective operations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality–IT–Digital Integration\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary interface between Quality, IT, and Data/AI teams, translating business needs into scalable digital solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure integration with enterprise platforms (e.g., SAP, LIMS, MES) and support implementation of emerging technologies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operational Excellence \u0026amp;amp; Transformation\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as a Quality Operational Excellence Champion, driving process simplification, standardization, and cycle time improvements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Eliminate non-value-added activities and improve right-first-time performance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and track metrics for system effectiveness, adoption, and process efficiency\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Business System Governance\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the QMS Business System Governance process, including ownership, accountability, and prioritization of enhancements for the QMS systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in governance forums (e.g., Digital Steering Committees, System Boards)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary escalation point for systemic Quality System issues\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leadership \u0026amp;amp; Culture\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as a thought leader in modern Quality Systems, advancing innovation and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of open-minded thinking, accountability, and innovation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hold teams accountable for system utilization and performance outcomes, while empowering new ideas and approaches\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;12+ years of biopharmaceutical experience with leadership in Quality Systems and Compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience as a Business System Owner / Digital Process Owner in a GxP environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong expertise in global GxP regulations and ability to translate requirements into practical solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with enterprise systems (eQMS, DMS, LMS, SAP, LIMS, MES); experience with Veeva Vault is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience driving digital transformation, automation, and advanced analytics initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with AI/ML tools and digital quality solutions in regulated environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of data integrity, CSV/CSA, and digital system compliance requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to influence across functions and drive system adoption, performance improvements, and inspection readiness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated leadership in operational excellence, accountability, and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate effectively in a fully digital, data-driven environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $190,000 - $260,000. This range is a good faith estimate of the expected salary\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025603004,"name":"Quality Assurance ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6021047004?gh_jid=6021047004","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":5165846004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Employee","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Regular","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6021047004,"updated_at":"2026-06-12T11:43:46-04:00","requisition_id":"P100808","title":"Lead Technician, Facilities","company_name":"ElevateBio","first_published":"2026-06-12T11:43:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;The Role:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is seeking a Lead Maintenance Technician. The successful candidate will be detailed oriented, organized, and have a strong desire to learn. Key responsibilities will be performing or overseeing vendor performed maintenance/calibrations on GMP Utility systems, process equipment and clean room infrastructure in a highly regulated cGMP environment. The candidate must be willing to support on-call rotation and support additional shift coverage as needed including annual shutdown support.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Here’s What You’ll Do:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Utilizes CMMS to manage the completion of all maintenance assignments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comply with Good Manufacturing Practices (GMP) requirements to include detailed documentation of work performed in both electronic and written form.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reports any maintenance failure or issues immediately to management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluates equipment performance and makes recommendations to maintenance performance or system design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Seeks to continuously improve maintenance practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interpret P\u0026amp;amp;IDs, equipment/system layouts, wiring diagrams, and specifications to plan and perform maintenance and repair activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides support during annual shutdowns.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine performance of preventative maintenance on process support systems and equipment including but not limited to: Pumps, Valves, Autoclaves, Centrifuges, Reactors, BSC\u0026#39;s, Isolators, WFI Generation/Distribution, Clean Steam, compressed gases, HVAC equipment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducts rounds of GMP and non-GMP equipment and systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Inspect, operate, or test machinery or equipment to diagnose machine malfunctions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform routine maintenance, such as inspecting drives, motors, or belts, checking fluid levels, replacing filters, or doing other preventive maintenance actions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Diagnose mechanical problems and determine how to correct them, checking blueprints, repair manuals, or parts catalogs, as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Repair machines, equipment, or structures, using tools such as hammers, hoists, saws, drills, wrenches, or equipment such as precision measuring instruments or electrical or electronic testing devices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain or repair specialized equipment or machinery located in cafeterias, laundries, hospitals, stores, offices, or factories.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assemble, install, or repair wiring, electrical or electronic components, pipe systems, plumbing, machinery, or equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains all spaces clean and orderly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinating and escorting contractors and vendors for the performance of preventative maintenance and repairs on process support systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports quality systems for CAPA, Deviations and Change Management. Dismantle machines, equipment, or devices to access and remove defective parts, using hoists, cranes, hand tools, or power tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Annual Shutdown, On-Call rotation and shift coverage.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to perform all work in a safe manner. The ability and desire to excel in a fast paced, inclusive team environment which prides itself on providing the highest level of service to our internal customers. Desire to interact in a professional, helpful manner with staff at all levels within the organization on a regular basis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Train and mentor maintenance staff on equipment operation, maintenance procedures and safety protocols.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High School diploma, GED, or equivalent required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trade school or undergraduate education is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professionally Licensed in any of the following areas desirable: Wastewater Treatment, Plumbing, Electrical, Refrigeration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 + years of applicable experience in a GMP environment is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multitask and always maintain professionalism\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office products (Outlook, Word, Excel, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with Blue Mountain RAM or other CMMS programs preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with DeltaV PCS System or other control system is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, understand, and follow SOP, P\u0026amp;amp;ID\u0026#39;s and work instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills in both oral and written reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in Quality Systems with Deviations, CAPAs, and Change Controls\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $50/hour - $69/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025596004,"name":"Facilities and Engineering ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/5161635004?gh_jid=5161635004","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":"United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":null,"value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":null,"value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":null,"value_type":"single_select"}],"id":5161635004,"updated_at":"2026-03-27T15:50:24-04:00","requisition_id":null,"title":"Not seeing what you're looking for? Join Our Talent Community!","company_name":"ElevateBio","first_published":"2024-05-06T17:09:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Our Team\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are a group of explorers who share a passion for constant discovery and cutting-edge technologies. We are committed to strengthen and accelerate the development of life-transforming therapies. We welcome individuals who are dedicated, driven, and eager to make an impact in their field. Whether you\u0026#39;re a seasoned leader or just starting your career journey, we offer a wide range of roles across various disciplines. From R\u0026amp;amp;D, Manufacturing, General \u0026amp;amp; Administrative and more, we are always looking to connect with exceptional people who are intrigued about the potential of joining our team.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Our Values\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ingenuity with Intention\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaboration Without Borders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;No Pretense— Full Transparency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Courageously Curious\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respect Perspective\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Behind our successful team are the values we place front and center of everything we do. These five principles are our due north that support our vision, set our culture, and solidify what we stand for. As our team expands, we are seeking individuals who embody these principles. Sound like you? If so, we\u0026#39;d love to hear from you!\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Awards \u0026amp;amp; Recognition:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Join a team that has been recognized for excellence in innovation and culture. View some of our proudest company achievements below:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;2021 –\u0026amp;nbsp;\u0026lt;a href=\u0026quot;https://ispe.org/facility-year-awards/winners/2021/operational-excellence\u0026quot;\u0026gt;ISPE Facility of the Year for Operational Excellence\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2021 – \u0026lt;a href=\u0026quot;https://www.cnbc.com/2021/05/25/elevate-bio-disruptor-50.html\u0026quot;\u0026gt;CNBC Disruptor 50\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2022 – \u0026lt;a href=\u0026quot;https://www.bostonglobe.com/2022/11/30/magazine/top-45-large-employers-massachusetts-2022/?p1=Article_Inline_Text_Link\u0026quot;\u0026gt;The Boston Globe Top Place to Work\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2023 – \u0026lt;a href=\u0026quot;https://www2.deloitte.com/content/dam/Deloitte/us/Documents/technology-media-telecommunications/2023-fast-500-winners-list-v1.1.pdf\u0026quot;\u0026gt;Deloitte Technology Fast 500\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2023 – \u0026lt;a href=\u0026quot;https://www.cnbc.com/2023/05/09/elevatebio-disruptor-50.html\u0026quot;\u0026gt;CNBC Disruptors 50\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2023 – \u0026lt;a href=\u0026quot;https://www.bostonglobe.com/2023/11/29/magazine/top-large-companies-to-work-for-in-massachusetts/\u0026quot;\u0026gt;The Boston Globe Top Place to Work\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2024 – \u0026lt;a href=\u0026quot;https://www.fastcompany.com/91034883/biotech-most-innovative-companies-2024\u0026quot;\u0026gt;Fast Company Most Innovative Companies in Biotech\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2024 – \u0026lt;a href=\u0026quot;https://www.cnbc.com/2024/05/14/elevatebio-cnbc-disruptor-50.html\u0026quot;\u0026gt;CNBC Disruptor 50\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2025 – \u0026lt;a href=\u0026quot;https://www.cnbc.com/2025/06/10/elevatebio-cnbc-disruptor-50.html\u0026quot;\u0026gt;CNBC Disruptor 50\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2025 – \u0026lt;a href=\u0026quot;https://elevate.bio/press-releases/elevatebio-basecamp-achieves-icmc-certification-for-commercial-cell-and-gene-therapy-manufacturing-capabilities/\u0026quot;\u0026gt;ICMC Certification for Commercial Cell and Gene Therapy Manufacturing Capabilities\u0026lt;/a\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[],"offices":[]},{"absolute_url":"https://elevate.bio/about/jobs/6021068004?gh_jid=6021068004","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":5165855004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Contingent Worker","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Contractor","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6021068004,"updated_at":"2026-06-12T12:11:29-04:00","requisition_id":"P100810","title":"Senior Associate Process Engineer (Contract)","company_name":"ElevateBio","first_published":"2026-06-12T12:11:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;The Role:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a Senior Associate Process Engineer within the Manufacturing Science and Technology (MSAT) organization.\u0026amp;nbsp; As a Senior Associate Process Engineer in MSAT, you will provide process science support for GMP manufacturing, technology transfers, development studies, characterization, validation, and continuous improvement projects within a highly matrixed cross-functional team for ElevateBio programs. \u0026amp;nbsp;As part of support, you will write protocols, product impact assessments, root-cause analysis reports, and technical reports. You will additionally support data collection and charting for non-GMP and GMP batches. This position is a 6-month contract.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Here’s What You’ll Do:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work cross-functionally across Process Development, Manufacturing, Quality, and Supply Chain to provide support for technology transfers and cGMP manufacturing for both clinical and commercial stage programs across modalities including cell and gene therapy, mRNA and viral vector.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Authoring and reviewing technical documentation related to manufacturing activities including protocols, technical reports, work instructions, SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and support quality events such as deviations, investigations, CAPAs, and Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the root cause determination of process-related deviations in a timely and complete manner. The candidate will work with a cross-functional team to resolve complex problems using experience and efficient application of scientific methodology and technical reasoning, then propose comprehensive process solutions and improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support gap analyses and risk assessments to support the capital projects and tech transfers.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s Degree in Life Sciences, Engineering, Biotechnology, or a related technical discipline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in a MSAT, Manufacturing, or Process Development role\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell culture, and process development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in cell and gene therapy, aseptic processing, and drug manufacturing preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of process development, validation, and lifecycle management to support comparability studies, process validation, and licensure changes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills and ability to work cross-functionally with technical and quality teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with electronic systems used in GMP environments such as Veeva, or electronic batch records\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $43/hour - $57/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4081558004,"name":"MSAT","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6010594004?gh_jid=6010594004","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":5160840004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Employee","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Regular","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6010594004,"updated_at":"2026-06-02T11:52:31-04:00","requisition_id":"P100798","title":"Supervisor, Manufacturing","company_name":"ElevateBio","first_published":"2026-06-02T11:51:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is looking for a dynamic individual to join and, contribute to building the manufacturing operations team at our BaseCamp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, TILs, and mRNA. The individual should be a motivated self-starter eager to contribute to supporting a manufacturing organization unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Here’s What You’ll Do:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, expansion, harvest, cryopreservation and final product visual inspection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead manufacturing activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively with cross functional teams comprised of process development, facilities \u0026amp;amp; engineering, MSAT, quality control and quality assurance to ensure right-first-time technology transfer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Quality Assurance and MSAT to proactively resolve issues such as deviations, CAPAs, Change Controls.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to the highest safety and quality standards in service of our colleagues and patients.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify opportunities for improvements in areas such as safety, quality, delivery and cost.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be integral in providing hands-on technical, organizational, and leadership expertise to the manufacturing department including but not limited to equipment selection, SOPs, batch records, reports, risk assessments, material ordering/management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the safety of assigned areas and work practices in accordance with EHS program. Ensure JHA (Job Hazard Analysis) are reviewed regularly, and pre-job briefs are in place prior to execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide daily management oversight for the team and ensure process are executed with cGMP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recruit and develop staff, maintain, and report department metrics to drive operational improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Balance and prioritize daily production demands to ensure right first-time execution.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in biological science(s) field or related engineering with 4-6 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of experience in people leading and/or project leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with some or all of the following: cGMP manufacture and/or process development for CART, TCR, TIL, cellular therapies, and mRNA.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced understanding of primary cell culture and experience with equipment including but not limited to BSC, Microscope, LOVO, CliniMACS, Incubators, Centrifuges, CRF, and G-Rex systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding communication skills (verbal and written).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate proficiency in aseptic technique and/or processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to function in dynamic environment and balance multiple priorities simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Rotating 12-hour day shifts (0700-1900).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be available to overtime on weekdays, weekends and holidays as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employee will frequently stand, walk, bend, stretch for extended periods.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely carry up to 25 pounds and up to 50 pounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine repetitive use of arms/wrist/hands.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work nights, weekends, holidays as needed to support business needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to don job-specific PPE.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $50/hour - $69/hour. This range is a good faith estimate of the expected hourly range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025594004,"name":"Manufacturing ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6021026004?gh_jid=6021026004","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":5165836004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Employee","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Regular","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6021026004,"updated_at":"2026-06-12T11:51:30-04:00","requisition_id":"P100807","title":"Technician II, Facilities","company_name":"ElevateBio","first_published":"2026-06-12T11:51:30-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;The Role:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;ElevateBio is seeking an experienced Facilities Technician II to join the team. The successful candidate will be detailed oriented, organized, and have a strong desire to learn. Key responsibilities will be performing or overseeing vendor performed maintenance/calibrations on GMP Utility systems, process equipment and clean room infrastructure in a highly regulated cGMP environment. The candidate must be willing to support on-call rotation and support additional shift coverage as needed including annual shutdown support.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Here’s What You’ll Do:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Utilizes CMMS to manage the completion of all maintenance assignments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comply with Good Manufacturing Practices (GMP) requirements to include detailed documentation of work performed in both electronic and written form.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reports any maintenance failure or issues immediately to management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluates equipment performance and makes recommendations to maintenance performance or system design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Seeks to continuously improve maintenance practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interpret P\u0026amp;amp;IDs, equipment/system layouts, wiring diagrams, and specifications to plan and perform maintenance and repair activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides support during annual shutdowns.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Routine performance of preventative maintenance on process support systems and equipment including but not limited to: Pumps, Valves, Autoclaves, Centrifuges, Reactors, BSC\u0026#39;s, Isolators, WFI Generation/Distribution, Clean Steam, compressed gases, HVAC equipment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducts rounds of GMP and non-GMP equipment and systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Inspect, operate, or test machinery or equipment to diagnose machine malfunctions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform routine maintenance, such as inspecting drives, motors, or belts, checking fluid levels, replacing filters, or doing other preventive maintenance actions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Diagnose mechanical problems and determine how to correct them, checking blueprints, repair manuals, or parts catalogs, as necessary.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Repair machines, equipment, or structures, using tools such as hammers, hoists, saws, drills, wrenches, or equipment such as precision measuring instruments or electrical or electronic testing devices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain or repair specialized equipment or machinery located in cafeterias, laundries, hospitals, stores, offices, or factories.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assemble, install, or repair wiring, electrical or electronic components, pipe systems, plumbing, machinery, or equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains all spaces clean and orderly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinating and escorting contractors and vendors for the performance of preventative maintenance and repairs on process support systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports quality systems for CAPA, Deviations and Change Management. Dismantle machines, equipment, or devices to access and remove defective parts, using hoists, cranes, hand tools, or power tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Annual Shutdown, On-Call rotation and shift coverage.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to perform all work in a safe manner. The ability and desire to excel in a fast paced, inclusive team environment which prides itself on providing the highest level of service to our internal customers. Desire to interact in a professional, helpful manner with staff at all levels within the organization on a regular basis.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High School diploma, GED, or equivalent required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trade school or undergraduate education is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professionally Licensed in any of the following areas desirable: Wastewater Treatment, Plumbing, Electrical, Refrigeration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;1 + years of applicable experience in a GMP environment is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multitask and always maintain professionalism\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office products (Outlook, Word, Excel, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with Blue Mountain RAM or other CMMS programs preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with DeltaV PCS System or other control system is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, understand, and follow SOP, P\u0026amp;amp;ID\u0026#39;s and work instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills in both oral and written reports\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $48/hour - $62/hour. This range is a good faith estimate of the expected hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025596004,"name":"Facilities and Engineering ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]},{"absolute_url":"https://elevate.bio/about/jobs/6021046004?gh_jid=6021046004","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":5165845004,"location":{"name":"Waltham, Massachusetts, United States"},"metadata":[{"id":4197149004,"name":"Employment Type","value":"Employee","value_type":"single_select"},{"id":6931082004,"name":"Employee Type","value":"Regular","value_type":"single_select"},{"id":5740262004,"name":"Location of Position","value":"Waltham, MA - Smith","value_type":"single_select"}],"id":6021046004,"updated_at":"2026-06-12T11:57:34-04:00","requisition_id":"P100809","title":"Technician I, Metrology","company_name":"ElevateBio","first_published":"2026-06-12T11:57:34-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;The Role:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This entry-level role supports calibration activities across process, laboratory, packaging, and utility instrumentation. The Technician I operates within the metrology program led by Metrology Leadership, performing hands-on calibrations, maintaining in-house standards, documenting work in the CMMS, and supporting third-party vendors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Here’s What You’ll Do:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform routine calibrations and basic troubleshooting per SOPs and work instructions under guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute and document work orders in the CMMS (e.g., Blue Mountain RAM) accurately and on time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with scheduling, escorting, and supporting third-party calibration vendors and equipment owners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain, stage, and care for in-house standards, tools, and reference materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support initial equipment setup, labeling, and status control.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in continuous improvement, training, and 5S activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Spend approximately 75% hands-on in the field and 25% on documentation/administrative tasks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;2-year technical/AA/AS degree in metrology, instrumentation, electronics, or equivalent training/experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read and follow SOPs, P\u0026amp;amp;IDs, and work instructions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Office (Outlook, Word, Excel).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail, organization, and communication.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with measurement fundamentals; exposure to measurement uncertainty is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a GMP environment and with Blue Mountain RAM or similar CMMS is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Environment:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work in controlled cleanroom areas with gowning and PPE; adhere to safety and contamination control procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasionally work in cold, wet, hot, or humid conditions, indoors and outdoors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasional work around chemicals (e.g., alcohols, acids, buffers, refrigerants) that may require respiratory protection.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to work routine 8-hour shifts; overtime/weekends/holidays as needed with notice.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Demands:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Frequent standing, walking, kneeling, climbing ladders/stairs, and accessing equipment in tight or elevated spaces.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manual dexterity for small parts, fittings, and test connections; visual and hearing acuity for instruments and alarms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Occasional repetitive bending/stooping; occasional lifting up to 50 pounds.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;\u0026lt;em\u0026gt;The budgeted range for this position is $43/hour - $57/hour. This range is a good faith estimate of the expected\u0026amp;nbsp;hourly\u0026amp;nbsp;range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025596004,"name":"Facilities and Engineering ","child_ids":[],"parent_id":null}],"offices":[{"id":4012768004,"name":"ElevateBio","location":"Waltham, Massachusetts, United States","child_ids":[4037934004],"parent_id":null}]}],"meta":{"total":15}}