Project Manager & Validation Specialist (Andover)

Validation Specialist & Project ManagerLocation: Wilmington, MA (On-site)Join my client's fast-growing radiopharmaceutical manufacturing expansion supporting breakthrough targeted cancer therapies. This high-impact contract role blends hands-on validation execution with full-scale project leadership in a regulated cGMP and NRC environment. If you thrive driving complex technical programs while staying close to the equipment and operations, this is your opportunity to own a mission-critical expansion from start to finish.Why You Should ApplyLead a major manufacturing expansion tied to advancements in nuclear medicineHigh-visibility role partnering with Quality, Operations, Engineering, and Radiation Safety teamsOwn both validation execution and project management strategyCompetitive hourly compensation commensurate with experience12–18 month contract engagement with meaningful technical impactWhat You'll Be DoingAuthor and execute DQ/IQ/OQ/PQ qualification protocolsOwn and maintain the detailed expansion project plan (Gantt), including all tasks, owners, dependencies, and milestone dates across validation, qualification, documentation, and equipment workstreamsDrive cross-functional teams and contractor deliverables to completionSupport GMP documentation including SOPs, MBRs, and validation recordsCoordinate FAT/SAT activities and manufacturing readiness effortsAbout YouBachelor's degree in Engineering, Life Sciences, or related fieldExperience executing equipment qualification in GMP manufacturingStrong knowledge of FDA cGMP regulations and documentation standardsProven ability managing Gantt schedules, risks, and technical project timelinesFamiliarity with radiopharmaceutical, sterile, or analytical equipment environments preferredHow To ApplyWe'd love to see your resume, but we don't need it to have a conversation. Send us an email to js@scientificsearch.com and tell me why you're interested. Or, feel free to email your resume. Please include Job#19885.