{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5999967004","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":4887407004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5999967004,"updated_at":"2026-06-02T10:22:59-04:00","requisition_id":"386","title":"CQV Consultant","company_name":"Valspec","first_published":"2026-05-19T12:04:50-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;CQV Consultant – Upstream / Downstream / CIP / PSE / Clean Utilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Holly Springs (100% Onsite)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt; Long-Term Contract\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Start Date:\u0026lt;/strong\u0026gt; ASAP\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Overview \u0026lt;/strong\u0026gt;We are seeking experienced CQV Consultants to support a major biopharmaceutical manufacturing project in Holly Springs, NC. This is a long-term onsite opportunity supporting commissioning, qualification, and validation activities across multiple process and utility systems in a GMP manufacturing environment.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;We are specifically looking for strong “A+” level consultants with hands-on pharmaceutical or biotech project experience supporting large-scale manufacturing operations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are hiring CQV professionals with experience in one or more of the following areas:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Upstream Processing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Downstream Processing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CIP (Clean-in-Place) Systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;PSE (Process Support Equipment)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean Utilities\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;Key Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute CQV lifecycle activities including commissioning, IQ/OQ, and field verification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support startup and qualification of GMP manufacturing equipment and utility systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author, review, and execute validation documentation and protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with engineering, operations, quality, automation, and project teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support deviation investigations, change controls, and CAPA activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with GMP, FDA, and regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in walkdowns, system turnover, and punch-list resolution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate documentation in accordance with data integrity and quality standards\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;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prior CQV experience in pharmaceutical, biotech, or GMP-regulated manufacturing environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of commissioning and qualification processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting one or more of the following: Upstream, Downstream, CIP, PSE, or Clean Utilities systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with GMP documentation practices and regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work onsite in Holly Springs, NC on a full-time basis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and cross-functional collaboration skills\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;Preferred Experience\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Large-scale biologics or vaccine manufacturing projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Startup or greenfield facility experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with DeltaV, MES, or automated process systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of clean utilities including WFI, clean steam, compressed gases, and purified water systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017817004,"name":"Valpro","child_ids":[],"parent_id":null}],"offices":[{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764291004","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":4471057004,"location":{"name":"Royersford, Pennsylvania, United States"},"metadata":null,"id":5764291004,"updated_at":"2026-06-04T10:09:25-04:00","requisition_id":"218","title":"Equipment Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:15:20-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div\u0026gt;\u0026lt;hr\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Job Title:\u0026lt;/strong\u0026gt; GMP Equipment Validation Engineer – CQV\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated and detail-oriented GMP Equipment Validation Engineer to support Commissioning, Qualification, and Validation (CQV) activities for a range of manufacturing and utility equipment at a client site in Swiftwater, PA. This role is ideal for someone who thrives in a dynamic environment, can work independently, and is confident interfacing directly with client teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our CQV team collaborates closely with the client across multiple facets of controls and automation, ensuring seamless integration and compliance with regulatory standards. The ideal candidate will bring strong technical expertise, excellent communication skills, and a proactive approach to problem-solving. The ideal candidate has experience leading the equipment CQV efforts of a team that also includes computer system validation engineers and specialists.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Lead and execute CQV activities for GMP equipment including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Autoclaves\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CIP/SIP systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bioreactors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Incubators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Freezers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Refrigerators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Centrifuges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Washers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Controlled temperature units\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Environmental chambers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;HVAC systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean steam generators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;WFI systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process tanks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Utility systems (compressed air, nitrogen, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Develop and review validation documentation including URS, DQ, IQ, OQ, and PQ protocols and reports.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Perform risk assessments and impact analyses to support validation strategy.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Coordinate with client engineering, automation, and quality teams to ensure alignment on project goals and timelines.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Troubleshoot and resolve equipment and process issues during commissioning and qualification phases.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Maintain compliance with cGMP, FDA, and other applicable regulatory requirements.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Provide timely updates and communicate effectively with client stakeholders.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in engineering, Life Sciences, or related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in CQV within a GMP-regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of validation lifecycle and regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automated systems and controls integration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and manage multiple priorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;This is an excellent opportunity for anyone who can be onsite in NEPA and lead equipment CQV efforts, along with another team that is performing computer system validation. We will need others to be staff validation engineers in the future as well, but this is for someone who can work independently and provide some leadership on the technical side. Apply if interested.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null},{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764295004","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":4471057004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5764295004,"updated_at":"2026-06-04T10:09:25-04:00","requisition_id":"218","title":"Equipment Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:15:24-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div\u0026gt;\u0026lt;hr\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Job Title:\u0026lt;/strong\u0026gt; GMP Equipment Validation Engineer – CQV\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: Indianapolis, IN\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated and detail-oriented GMP Equipment Validation Engineer to support Commissioning, Qualification, and Validation (CQV) activities for a range of manufacturing and utility equipment at a client site. This role is ideal for someone who thrives in a dynamic environment, can work independently, and is confident interfacing directly with client teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our CQV team collaborates closely with the client across multiple facets of controls and automation, ensuring seamless integration and compliance with regulatory standards. The ideal candidate will bring strong technical expertise, excellent communication skills, and a proactive approach to problem-solving. The ideal candidate has experience leading the equipment CQV efforts of a team that also includes computer system validation engineers and specialists.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Lead and execute CQV activities for GMP equipment including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Autoclaves\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CIP/SIP systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bioreactors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Incubators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Freezers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Refrigerators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Centrifuges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Washers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Controlled temperature units\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Environmental chambers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;HVAC systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean steam generators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;WFI systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process tanks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Utility systems (compressed air, nitrogen, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Develop and review validation documentation including URS, DQ, IQ, OQ, and PQ protocols and reports.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Perform risk assessments and impact analyses to support validation strategy.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Coordinate with client engineering, automation, and quality teams to ensure alignment on project goals and timelines.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Troubleshoot and resolve equipment and process issues during commissioning and qualification phases.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Maintain compliance with cGMP, FDA, and other applicable regulatory requirements.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Provide timely updates and communicate effectively with client stakeholders.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in engineering, Life Sciences, or related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in CQV within a GMP-regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of validation lifecycle and regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automated systems and controls integration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and manage multiple priorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;This is an excellent opportunity for anyone who can be onsite in NEPA and lead equipment CQV efforts, along with another team that is performing computer system validation. We will need others to be staff validation engineers in the future as well, but this is for someone who can work independently and provide some leadership on the technical side. Apply if interested.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null},{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764294004","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":4471057004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5764294004,"updated_at":"2026-06-04T10:09:25-04:00","requisition_id":"218","title":"Equipment Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:15:23-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div\u0026gt;\u0026lt;hr\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Job Title:\u0026lt;/strong\u0026gt; GMP Equipment Validation Engineer – CQV\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: Oceanside, CA\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated and detail-oriented GMP Equipment Validation Engineer to support Commissioning, Qualification, and Validation (CQV) activities for a range of manufacturing and utility equipment at a client site. This role is ideal for someone who thrives in a dynamic environment, can work independently, and is confident interfacing directly with client teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our CQV team collaborates closely with the client across multiple facets of controls and automation, ensuring seamless integration and compliance with regulatory standards. The ideal candidate will bring strong technical expertise, excellent communication skills, and a proactive approach to problem-solving. The ideal candidate has experience leading the equipment CQV efforts of a team that also includes computer system validation engineers and specialists.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Lead and execute CQV activities for GMP equipment including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Autoclaves\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CIP/SIP systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bioreactors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Incubators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Freezers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Refrigerators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Centrifuges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Washers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Controlled temperature units\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Environmental chambers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;HVAC systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean steam generators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;WFI systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process tanks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Utility systems (compressed air, nitrogen, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Develop and review validation documentation including URS, DQ, IQ, OQ, and PQ protocols and reports.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Perform risk assessments and impact analyses to support validation strategy.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Coordinate with client engineering, automation, and quality teams to ensure alignment on project goals and timelines.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Troubleshoot and resolve equipment and process issues during commissioning and qualification phases.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Maintain compliance with cGMP, FDA, and other applicable regulatory requirements.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Provide timely updates and communicate effectively with client stakeholders.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in engineering, Life Sciences, or related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in CQV within a GMP-regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of validation lifecycle and regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automated systems and controls integration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and manage multiple priorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;This is an excellent opportunity for anyone who can be onsite in NEPA and lead equipment CQV efforts, along with another team that is performing computer system validation. We will need others to be staff validation engineers in the future as well, but this is for someone who can work independently and provide some leadership on the technical side. Apply if interested.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null},{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764293004","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":4471057004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5764293004,"updated_at":"2026-06-04T10:09:25-04:00","requisition_id":"218","title":"Equipment Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:15:22-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;hr\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Job Title:\u0026lt;/strong\u0026gt; GMP Equipment Validation Engineer – CQV\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: Raleigh, NC\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Overview:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated and detail-oriented GMP Equipment Validation Engineer to support Commissioning, Qualification, and Validation (CQV) activities for a range of manufacturing and utility equipment at a client site. This role is ideal for someone who thrives in a dynamic environment, can work independently, and is confident interfacing directly with client teams.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our CQV team collaborates closely with the client across multiple facets of controls and automation, ensuring seamless integration and compliance with regulatory standards. The ideal candidate will bring strong technical expertise, excellent communication skills, and a proactive approach to problem-solving. The ideal candidate has experience leading the equipment CQV efforts of a team that also includes computer system validation engineers and specialists.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Lead and execute CQV activities for GMP equipment including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Autoclaves\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CIP/SIP systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bioreactors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Incubators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Freezers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Refrigerators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Centrifuges\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Washers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Controlled temperature units\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Environmental chambers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;HVAC systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean steam generators\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;WFI systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process tanks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Utility systems (compressed air, nitrogen, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Develop and review validation documentation including URS, DQ, IQ, OQ, and PQ protocols and reports.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Perform risk assessments and impact analyses to support validation strategy.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Coordinate with client engineering, automation, and quality teams to ensure alignment on project goals and timelines.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Troubleshoot and resolve equipment and process issues during commissioning and qualification phases.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Maintain compliance with cGMP, FDA, and other applicable regulatory requirements.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;p\u0026gt;Provide timely updates and communicate effectively with client stakeholders.\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in engineering, Life Sciences, or related field.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in CQV within a GMP-regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of validation lifecycle and regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automated systems and controls integration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational and communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and manage multiple priorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;This is an excellent opportunity for anyone who can be onsite in NEPA and lead equipment CQV efforts, along with another team that is performing computer system validation. We will need others to be staff validation engineers in the future as well, but this is for someone who can work independently and provide some leadership on the technical side. Apply if interested.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null},{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5092765004","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":4646582004,"location":{"name":"Royersford, Pennsylvania, United States"},"metadata":null,"id":5092765004,"updated_at":"2026-06-04T10:32:43-04:00","requisition_id":"310","title":"General Application or Referral","company_name":"Valspec","first_published":"2024-02-26T13:32:14-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;GENERAL APPLICATION OR REFERRAL\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This posting is for those candidates who do not fit into any of our posted job opportunities for Proconex, Valspec, AVS, or Valpro. A Valspec Talent Relationship Manager representing Proconex, Valspec, AVS, and Valpro may conduct an initial phone screening if there is the possibility of a suitable opportunity in the near future. If there is nothing available that is a fit currently, the candidate will remain in our database for future opportunities.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013167004,"name":"Administrative","child_ids":[],"parent_id":4013162004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5968602004","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":4678666004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5968602004,"updated_at":"2026-06-02T10:22:59-04:00","requisition_id":"326","title":"Owner's Agent - Technical Project Manager","company_name":"Valspec","first_published":"2026-04-13T11:34:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Technical Project Manager / Owner’s Agent – Pharma Manufacturing Systems (MES / NYMI Band)\u0026lt;/strong\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Onsite / Hybrid (Pharma Manufacturing Site)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Industry:\u0026lt;/strong\u0026gt; Pharmaceutical / Biotech Manufacturing\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Focus Areas:\u0026lt;/strong\u0026gt; MES, PI Historian, OT/IT Systems, Networked Manufacturing Applications\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Role Overview\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a \u0026lt;strong\u0026gt;Technical Project Manager / Owner’s Agent\u0026lt;/strong\u0026gt; to lead the delivery of \u0026lt;strong\u0026gt;manufacturing digital systems\u0026lt;/strong\u0026gt; within a \u0026lt;strong\u0026gt;GMP pharmaceutical production environment\u0026lt;/strong\u0026gt;. This role is highly technical and hands-on, serving as the bridge between \u0026lt;strong\u0026gt;shop floor automation teams, Quality, and Corporate IT\u0026lt;/strong\u0026gt; to ensure systems are implemented, validated, and released without compromising \u0026lt;strong\u0026gt;product quality, data integrity, or regulatory compliance\u0026lt;/strong\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate has deep experience in \u0026lt;strong\u0026gt;MES, data historians, and OT/IT infrastructure\u0026lt;/strong\u0026gt;, paired with a strong understanding of \u0026lt;strong\u0026gt;CSV and global GMP regulations\u0026lt;/strong\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h3\u0026gt;Key Responsibilities\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as the \u0026lt;strong\u0026gt;Owner’s Representative\u0026lt;/strong\u0026gt; for manufacturing systems projects from design through implementation and validation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead delivery of \u0026lt;strong\u0026gt;MES / NYMI-band systems\u0026lt;/strong\u0026gt; supporting regulated manufacturing operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate \u0026lt;strong\u0026gt;IO / OT network design, implementation, testing, and commissioning\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee deployment and lifecycle management of:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;OSI PI (PI Data Historian)\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;ThinManager and mobile HMI cart environments\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;FactoryTalk AssetCentre\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Siemens Simatic Logon Server\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary interface between:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Automation \u0026amp;amp; Manufacturing teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality \u0026amp;amp; Validation groups\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Corporate IT and cybersecurity teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;External system integrators and vendors\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all systems are delivered in accordance with \u0026lt;strong\u0026gt;GMP, CSV, and Data Integrity requirements\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage scope, schedule, risks, and cross-functional dependencies in a regulated environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h3\u0026gt;Core Technical Requirements\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Manufacturing Execution Systems (MES):\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Hands-on project experience with \u0026lt;strong\u0026gt;Werum PAS‑X, Siemens Opcenter, or equivalent platforms\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Data Historians:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Strong experience with \u0026lt;strong\u0026gt;OSI PI (PI System)\u0026lt;/strong\u0026gt; for real-time data capture, reporting, and KPI analysis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;OT / IT Integration:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Solid understanding of \u0026lt;strong\u0026gt;DCS, PLCs, industrial networks, and SAP/ERP interfaces\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Industrial Infrastructure:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Experience overseeing \u0026lt;strong\u0026gt;backup, recovery, and high-availability architectures\u0026lt;/strong\u0026gt; for manufacturing systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h3\u0026gt;Regulatory \u0026amp;amp; Compliance Expertise\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Computer System Validation (CSV):\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Strong working knowledge of \u0026lt;strong\u0026gt;GAMP 5\u0026lt;/strong\u0026gt; and risk-based validation approaches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Regulatory Compliance:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Experience supporting systems subject to:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;FDA 21 CFR Part 11\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;EU GMP Annex 11\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Data Integrity:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Understanding of \u0026lt;strong\u0026gt;ALCOA+ principles\u0026lt;/strong\u0026gt; and electronic records management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Quality Systems:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Familiarity with \u0026lt;strong\u0026gt;Change Control, Deviations, and CAPA\u0026lt;/strong\u0026gt; within GMP environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h3\u0026gt;Qualifications\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Education:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Bachelor’s degree in \u0026lt;strong\u0026gt;Engineering, Computer Science, or Life Sciences\u0026lt;/strong\u0026gt; required\u0026lt;br\u0026gt;Master’s degree or MBA preferred for senior-level candidates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Experience:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;5–8+ years\u0026lt;/strong\u0026gt; of project management experience within \u0026lt;strong\u0026gt;pharma or biotech manufacturing\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Certifications (Preferred):\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;PMP, Lean Six Sigma Green/Black Belt, or equivalent\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Soft Skills:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Proven ability to coordinate across technical, quality, and business stakeholders\u0026lt;br\u0026gt;Strong communication and documentation skills in regulated environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h3\u0026gt;Why This Role?\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead \u0026lt;strong\u0026gt;mission-critical manufacturing systems\u0026lt;/strong\u0026gt; that directly impact patient safety\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High-visibility role across \u0026lt;strong\u0026gt;Operations, Quality, and IT leadership\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Opportunity to influence \u0026lt;strong\u0026gt;digital plant and Industry 4.0 initiatives\u0026lt;/strong\u0026gt; in a GMP setting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work on complex, technically challenging projects at the intersection of automation and compliance\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4017817004,"name":"Valpro","child_ids":[],"parent_id":null}],"offices":[{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/6011552004","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":5161271004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":6011552004,"updated_at":"2026-06-02T14:32:59-04:00","requisition_id":"467","title":"Project Manager – North Carolina","company_name":"Valspec","first_published":"2026-06-02T14:16:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;CQV Project Manager – Life Sciences (NC)\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 Raleigh–Durham, NC\u0026lt;/p\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;We are hiring a \u0026lt;strong\u0026gt;CQV Project Manager\u0026lt;/strong\u0026gt; to lead commissioning, qualification, and validation projects within pharmaceutical and biotech manufacturing environments.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role combines \u0026lt;strong\u0026gt;hands-on CQV knowledge with project leadership\u0026lt;/strong\u0026gt;—owning validation execution, managing timelines, and ensuring systems are ready for GMP production.\u0026lt;/p\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead \u0026lt;strong\u0026gt;CQV execution\u0026lt;/strong\u0026gt; across equipment, utilities, and facility systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee \u0026lt;strong\u0026gt;IQ/OQ/PQ planning, execution, and closeout\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage \u0026lt;strong\u0026gt;project schedules, milestones, and deliverables\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive \u0026lt;strong\u0026gt;startup, system turnover, and validation readiness activities\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with engineering, QA, operations, and vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee validation documentation (protocols, reports, deviations, risk assessments)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify risks and ensure projects stay on track\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5–10+ years of experience in \u0026lt;strong\u0026gt;CQV, validation, or CQV project management\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong background in \u0026lt;strong\u0026gt;GMP environments + IQ/OQ/PQ\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Process equipment (CIP/SIP, fill/finish, upstream/downstream, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Utilities (WFI, clean steam, process gases)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facility systems (HVAC, cleanrooms)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to lead \u0026lt;strong\u0026gt;on-site CQV execution and cross-functional teams\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;strong\u0026gt;Nice to Have\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Startup or large capital project experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to CSV, MES, or automation systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;Apply today to learn more about this exciting new life sciences project management opportunity!\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/6000408004","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":5156610004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":6000408004,"updated_at":"2026-06-02T10:22:59-04:00","requisition_id":"465","title":"QA Consultant","company_name":"Valspec","first_published":"2026-05-19T16:48:45-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Automation QA Engineer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Remote \u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Employment Type:\u0026lt;/strong\u0026gt; Contract / Consulting (6-12+ months)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Start Date:\u0026lt;/strong\u0026gt; ASAP\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role: \u0026lt;/strong\u0026gt;We are seeking experienced Automation QA Engineers to support our clients in North Carolina. These roles will support automation quality assurance activities within a GMP-regulated pharmaceutical manufacturing environment, with a strong focus on commissioning, qualification, validation, and lifecycle documentation for automation systems.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;This is an excellent opportunity for candidates with pharmaceutical or biotech automation QA experience who are comfortable working cross-functionally with Validation, Engineering, Manufacturing, and Quality teams in support of large-scale capital and operational projects.\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide QA oversight and support for automation-related qualification and validation activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve validation lifecycle documentation including:\u0026lt;/li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;IQ/OQ/PQ protocols and reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Risk assessments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Traceability matrices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Change controls\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deviations and CAPAs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;Support automation systems operating within GMP manufacturing environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with FDA, cGMP, GAMP 5, and 21 CFR Part 11 requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Automation, CQV, CSV, Manufacturing, and Quality teams to ensure compliant execution of project deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in document reviews, project meetings, and quality assessments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support audit readiness and inspection preparedness activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with implementation and continuous improvement of validation and QA processes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Systems / Technologies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Experience with one or more of the following is highly preferred:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;DeltaV\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Rockwell / PLC systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;SCADA or HMI platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;MES systems (Syncade experience is a plus)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Historian systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Automated manufacturing equipment within pharma/biotech environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Engineering, Life Sciences, Computer Science, or related field preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of experience in Automation QA, CSV, CQV, or Validation within the pharmaceutical, biotech, or regulated manufacturing industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of GMP compliance and validation lifecycle principles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience reviewing and approving GMP documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with data integrity and 21 CFR Part 11 requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and cross-functional collaboration skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently in a remote environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5969983004","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":4625796004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5969983004,"updated_at":"2026-06-02T10:22:59-04:00","requisition_id":"299","title":"Senior MES Engineer","company_name":"Valspec","first_published":"2026-04-14T14:34:39-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;MES Implementation Engineer – Apprentice.io Tempo\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Life Sciences | Systems Integration / Consulting\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Overview\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are building a delivery team to \u0026lt;strong\u0026gt;design, configure, deploy, and scale Apprentice.io’s Tempo Manufacturing Execution System (MES)\u0026lt;/strong\u0026gt; for large life sciences manufacturing clients. This role sits in a \u0026lt;strong\u0026gt;hands-on consulting delivery environment\u0026lt;/strong\u0026gt;, working directly with manufacturing, quality, automation, and IT stakeholders to move sites from paper or legacy MES to a modern, cloud-native execution platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a \u0026lt;strong\u0026gt;delivery-focused role\u0026lt;/strong\u0026gt; centered on \u0026lt;strong\u0026gt;process mapping, EBR/recipe configuration, integrations, validation support, and go‑live execution\u0026lt;/strong\u0026gt; in regulated (GxP) manufacturing environments.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead \u0026lt;strong\u0026gt;process discovery and design workshops\u0026lt;/strong\u0026gt; with client manufacturing, MS\u0026amp;amp;T, QA, QC, Automation, and IT teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate \u0026lt;strong\u0026gt;paper and hybrid batch records\u0026lt;/strong\u0026gt; into executable \u0026lt;strong\u0026gt;Electronic Batch Records (EBRs)\u0026lt;/strong\u0026gt; within Apprentice Tempo.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Configure Tempo objects including \u0026lt;strong\u0026gt;procedures, recipes, batches, equipment, materials, exceptions, and locations\u0026lt;/strong\u0026gt;.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author, test, and refine \u0026lt;strong\u0026gt;EBRs and recipes\u0026lt;/strong\u0026gt; in collaboration with end users to ensure usability, data integrity, and right‑first‑time execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support \u0026lt;strong\u0026gt;system integrations\u0026lt;/strong\u0026gt; (equipment status, master data, lab/QMS/ERP touchpoints) in coordination with client automation and IT teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Produce and maintain \u0026lt;strong\u0026gt;delivery and validation documentation\u0026lt;/strong\u0026gt; (URS, FRS, configuration specs, test evidence) aligned with client CSV expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute \u0026lt;strong\u0026gt;iterative build–test–demo cycles\u0026lt;/strong\u0026gt;, incorporating operator and QA feedback prior to qualification and go‑live.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support \u0026lt;strong\u0026gt;UAT, cutover planning, go‑live, and hypercare\u0026lt;/strong\u0026gt;, including rapid issue triage during early production runs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enable \u0026lt;strong\u0026gt;client ownership\u0026lt;/strong\u0026gt; through documentation, admin guides, and knowledge transfer as part of engagement closeout.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operate within an \u0026lt;strong\u0026gt;agile, consulting-style delivery model\u0026lt;/strong\u0026gt;, often supporting multi-site or phased MES deployments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Nice to Have \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with \u0026lt;strong\u0026gt;MES, EBR, or digital manufacturing systems\u0026lt;/strong\u0026gt; in life sciences (pharma, biotech, CGT, CDMO).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with \u0026lt;strong\u0026gt;GxP / CSV environments\u0026lt;/strong\u0026gt; and regulated manufacturing workflows.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfort working \u0026lt;strong\u0026gt;directly with clients\u0026lt;/strong\u0026gt; in a delivery or consulting capacity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior exposure to \u0026lt;strong\u0026gt;io Tempo\u0026lt;/strong\u0026gt; or other modern / no‑code MES platforms.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why This Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Client-facing delivery work with \u0026lt;strong\u0026gt;real ownership of MES outcomes\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to \u0026lt;strong\u0026gt;modern, cloud-native MES\u0026lt;/strong\u0026gt; (not legacy recipe coding)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Opportunity to support \u0026lt;strong\u0026gt;rapid deployments and multi-site scale‑outs\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong mix of \u0026lt;strong\u0026gt;process, technology, and manufacturing operations\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764168004","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":4033246004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5764168004,"updated_at":"2026-06-02T10:24:12-04:00","requisition_id":"2","title":"Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:10:31-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;VALIDATION ENGINEER\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: Oceanside, CA\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;(AUTOMATION, INFORMATION \u0026amp;amp; OPERATIONS TECHNOLOGY SOLUTIONS)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;VALSPEC is looking to identify top tier talent in the areas of automation and computer systems validation and system life cycle management. \u0026amp;nbsp;We are motivated to identify those that share our passion and can mirror the level of energy we put into ensuring that we remain on the cutting edge of the life sciences industry.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;We are looking for tech savvy professionals with a proven track record in the SDLC (system development life cycle) of automated computer systems within biopharmaceutical environments.\u0026amp;nbsp; Due to our unique approach in meeting the demands of our customers, we are pursuing both individuals that can join our team long term as well as SMEs (subject matter experts) that would like to join us on a consulting basis.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Overview\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role supports the execution of small projects or portions of larger projects. Supports the generation of quality assurance plans, verification plans, validation plans, and standard operating procedures as well as conduct risks assessments and participate in Quality/Regulatory audits. Develops and executes qualification protocols and final summary reports and may participate in commissioning activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience is highly preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automation, commissioning, qualification or operations in a cGMP environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience developing validation protocols and execution of protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of current industry standards such as GAMP5 and ASTM E2500.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tactical thinker with experience working with customers developing testing, validation and/or quality strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent client communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764282004","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":4033246004,"location":{"name":"Royersford, Pennsylvania, United States"},"metadata":null,"id":5764282004,"updated_at":"2026-06-02T10:24:12-04:00","requisition_id":"2","title":"Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:10:26-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;VALIDATION ENGINEER\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: Royersford, PA\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;(AUTOMATION, INFORMATION \u0026amp;amp; OPERATIONS TECHNOLOGY SOLUTIONS)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;VALSPEC is looking to identify top tier talent in the areas of automation and computer systems validation and system life cycle management. \u0026amp;nbsp;We are motivated to identify those that share our passion and can mirror the level of energy we put into ensuring that we remain on the cutting edge of the life sciences industry.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;We are looking for tech savvy professionals with a proven track record in the SDLC (system development life cycle) of automated computer systems within biopharmaceutical environments.\u0026amp;nbsp; Due to our unique approach in meeting the demands of our customers, we are pursuing both individuals that can join our team long term as well as SMEs (subject matter experts) that would like to join us on a consulting basis.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Overview\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role supports the execution of small projects or portions of larger projects. Supports the generation of quality assurance plans, verification plans, validation plans, and standard operating procedures as well as conduct risks assessments and participate in Quality/Regulatory audits. Develops and executes qualification protocols and final summary reports and may participate in commissioning activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience is highly preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automation, commissioning, qualification or operations in a cGMP environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience developing validation protocols and execution of protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of current industry standards such as GAMP5 and ASTM E2500.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tactical thinker with experience working with customers developing testing, validation and/or quality strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent client communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764169004","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":4033246004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5764169004,"updated_at":"2026-06-02T10:24:12-04:00","requisition_id":"2","title":"Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:10:33-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;VALIDATION ENGINEER\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: Indianapolis, IN\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;(AUTOMATION, INFORMATION \u0026amp;amp; OPERATIONS TECHNOLOGY SOLUTIONS)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;VALSPEC is looking to identify top tier talent in the areas of automation and computer systems validation and system life cycle management. \u0026amp;nbsp;We are motivated to identify those that share our passion and can mirror the level of energy we put into ensuring that we remain on the cutting edge of the life sciences industry.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;We are looking for tech savvy professionals with a proven track record in the SDLC (system development life cycle) of automated computer systems within biopharmaceutical environments.\u0026amp;nbsp; Due to our unique approach in meeting the demands of our customers, we are pursuing both individuals that can join our team long term as well as SMEs (subject matter experts) that would like to join us on a consulting basis.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Overview\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role supports the execution of small projects or portions of larger projects. Supports the generation of quality assurance plans, verification plans, validation plans, and standard operating procedures as well as conduct risks assessments and participate in Quality/Regulatory audits. Develops and executes qualification protocols and final summary reports and may participate in commissioning activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience is highly preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automation, commissioning, qualification or operations in a cGMP environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience developing validation protocols and execution of protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of current industry standards such as GAMP5 and ASTM E2500.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tactical thinker with experience working with customers developing testing, validation and/or quality strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent client communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5921836004","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":4033246004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5921836004,"updated_at":"2026-06-02T10:24:12-04:00","requisition_id":"2","title":"Validation Engineer","company_name":"Valspec","first_published":"2026-04-10T17:18:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Validation Engineer (Junior–Mid Level)\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026lt;strong\u0026gt;Employment Type:\u0026lt;/strong\u0026gt; W2 Contract (no C2C)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Duration:\u0026lt;/strong\u0026gt; Long-term contract (~1.5 years)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Start:\u0026lt;/strong\u0026gt; June shutdown timeframe\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Work Location:\u0026lt;/strong\u0026gt; Onsite / Hybrid at a GMP manufacturing site\n\u0026lt;h3\u0026gt;Job Description\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a \u0026lt;strong\u0026gt;Junior to Mid-Level Validation Engineer\u0026lt;/strong\u0026gt; for a \u0026lt;strong\u0026gt;W2 contract role\u0026lt;/strong\u0026gt; supporting a large-scale \u0026lt;strong\u0026gt;GMP manufacturing floor cybersecurity project\u0026lt;/strong\u0026gt; involving \u0026lt;strong\u0026gt;400+ devices\u0026lt;/strong\u0026gt;. This position will focus on \u0026lt;strong\u0026gt;validation execution\u0026lt;/strong\u0026gt;, \u0026lt;strong\u0026gt;GMP change control\u0026lt;/strong\u0026gt;, and \u0026lt;strong\u0026gt;IOQ testing\u0026lt;/strong\u0026gt; related to system and infrastructure changes in a regulated environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The role also supports \u0026lt;strong\u0026gt;SDLC-related documentation\u0026lt;/strong\u0026gt;, including \u0026lt;strong\u0026gt;Quality Assurance Plans (QAPs)\u0026lt;/strong\u0026gt;, and requires basic project coordination skills to support execution during planned manufacturing shutdowns. Senior validation and quality resources will provide oversight on more complex activities.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;Key Responsibilities\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute validation activities under \u0026lt;strong\u0026gt;GMP change control\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and/or execute \u0026lt;strong\u0026gt;IOQ protocols\u0026lt;/strong\u0026gt; and document test results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support \u0026lt;strong\u0026gt;SDLC-driven validation documentation\u0026lt;/strong\u0026gt;, including QAPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with planning and execution across multiple devices and systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track validation deliverables, testing readiness, and action items\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support audits, inspections, and documentation reviews as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Quality, Automation, IT/OT, and Engineering teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Required Qualifications\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Engineering, Science, or related field (or equivalent experience)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;1–5+ years\u0026lt;/strong\u0026gt; of validation or qualification experience in a \u0026lt;strong\u0026gt;GMP/GxP environment\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience executing validation protocols (IQ/OQ/IOQ or CSV-related testing)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of \u0026lt;strong\u0026gt;GMP documentation\u0026lt;/strong\u0026gt; and \u0026lt;strong\u0026gt;change control processes\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and technical writing skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Preferred Qualifications\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience validating \u0026lt;strong\u0026gt;computerized systems or OT/infrastructure\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with \u0026lt;strong\u0026gt;SDLC-controlled environments\u0026lt;/strong\u0026gt; and quality documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to \u0026lt;strong\u0026gt;21 CFR Part 11\u0026lt;/strong\u0026gt;, data integrity, or cybersecurity-related initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting validation work during \u0026lt;strong\u0026gt;manufacturing shutdowns\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Light project coordination or PM experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Contract Duration\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;This W2 contract supports a \u0026lt;strong\u0026gt;multi-phase project aligned with site shutdowns\u0026lt;/strong\u0026gt;, beginning in \u0026lt;strong\u0026gt;June\u0026lt;/strong\u0026gt;, continuing through \u0026lt;strong\u0026gt;December\u0026lt;/strong\u0026gt;, and concluding with a final phase in \u0026lt;strong\u0026gt;June 2027\u0026lt;/strong\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5764167004","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":4033246004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5764167004,"updated_at":"2026-06-02T10:24:12-04:00","requisition_id":"2","title":"Validation Engineer","company_name":"Valspec","first_published":"2026-01-14T11:10:30-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;VALIDATION ENGINEER\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: Raleigh, NC\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;(AUTOMATION, INFORMATION \u0026amp;amp; OPERATIONS TECHNOLOGY SOLUTIONS)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;VALSPEC is looking to identify top tier talent in the areas of automation and computer systems validation and system life cycle management. \u0026amp;nbsp;We are motivated to identify those that share our passion and can mirror the level of energy we put into ensuring that we remain on the cutting edge of the life sciences industry.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;We are looking for tech savvy professionals with a proven track record in the SDLC (system development life cycle) of automated computer systems within biopharmaceutical environments.\u0026amp;nbsp; Due to our unique approach in meeting the demands of our customers, we are pursuing both individuals that can join our team long term as well as SMEs (subject matter experts) that would like to join us on a consulting basis.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Overview\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role supports the execution of small projects or portions of larger projects. Supports the generation of quality assurance plans, verification plans, validation plans, and standard operating procedures as well as conduct risks assessments and participate in Quality/Regulatory audits. Develops and executes qualification protocols and final summary reports and may participate in commissioning activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience is highly preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with automation, commissioning, qualification or operations in a cGMP environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience developing validation protocols and execution of protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of current industry standards such as GAMP5 and ASTM E2500.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tactical thinker with experience working with customers developing testing, validation and/or quality strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent client communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013160004,"name":"Valspec - Engineering \u0026 Services","child_ids":[],"parent_id":4013159004}],"offices":[{"id":4006110004,"name":"Headquarters","location":"Royersford, Pennsylvania, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/valspec/jobs/5837198004","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":5068677004,"location":{"name":"Non-Headquarters"},"metadata":null,"id":5837198004,"updated_at":"2026-06-02T10:22:59-04:00","requisition_id":"458","title":"Validation Engineer - Kentucky","company_name":"Valspec","first_published":"2026-03-25T13:21:20-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Validation Engineer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Job Type: [Full-time/Contract]\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is seeking a highly motivated and detail-oriented Cleaning Validation Engineer to join our dynamic team. The successful candidate will play a crucial role in ensuring the cleanliness and compliance of our solid dose manufacturing processes through effective cleaning validation protocols.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop, execute, and oversee cleaning validation strategies and protocols for solid dose manufacturing equipment and processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams to establish cleaning validation requirements, ensuring alignment with regulatory standards and industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform risk assessments and gap analyses related to cleaning processes, proposing and implementing corrective actions as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and maintain cleaning validation documentation, including protocols, reports, and standard operating procedures (SOPs).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct equipment qualification activities in coordination with the validation team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and execute cleaning validation studies, ensuring thoroughness and accuracy in data collection and analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Investigate and resolve deviations related to cleaning processes, collaborating with Quality Assurance and Manufacturing teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay abreast of industry trends, regulatory requirements, and technological advancements in cleaning validation, providing recommendations for continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in regulatory inspections and audits, providing support and documentation as required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s or higher degree in a relevant scientific or engineering discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience in cleaning validation within the solid dose industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of regulatory guidelines and requirements related to cleaning validation (FDA, EMA, ICH, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of biopharmaceutical manufacturing processes and equipment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with risk-based approaches to cleaning validation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent documentation and record-keeping skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented with strong analytical and problem-solving abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communication skills and the ability to collaborate with cross-functional teams.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Certification in validation or related areas.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with solid dose and associated cleaning validation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join Valspec and contribute to the advancement of cutting-edge life sciences through your expertise in cleaning validation. We offer a collaborative and innovative work environment dedicated to fostering professional growth and development. Apply now to be a part of our dynamic team!\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Valspec?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation.\u0026amp;nbsp; We also offer a highly competitive benefits package, including:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Premium medical coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tuition reimbursement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unique performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more — all designed to support your growth, well-being, and future.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Join a team where your contributions matter, your development is prioritized, and your success is shared.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net\u0026amp;nbsp;or @valspec.net.\u0026amp;nbsp; Any other domains are impersonations and should be ignored.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Candidates must be legally eligible to work in the United States without company sponsorship.\u0026amp;nbsp; Also, we are not interested in working on a corp-to-corp basis with other companies at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4013159004,"name":"Valspec","child_ids":[4013421004,4013160004],"parent_id":null}],"offices":[{"id":4006249004,"name":"Non-Headquarters","location":null,"child_ids":[],"parent_id":null}]}],"meta":{"total":16}}