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Project Manager & Validation Specialist

Job

Scientific Search

Andover, MA (In Person)

Full-Time

Posted 1 week ago (Updated 11 hours ago) • Actively hiring

Expires 6/21/2026

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Job Description

Project Manager & Validation Specialist at Scientific Search Project Manager & Validation Specialist at Scientific Search in andover, Massachusetts Posted in 5 days ago.
Type:
full-time
Job Description:
Validation Specialist & Project Manager Location:
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 Apply Lead a major manufacturing expansion tied to advancements in nuclear medicine High-visibility role partnering with Quality, Operations, Engineering, and Radiation Safety teams Own both validation execution and project management strategy Competitive hourly compensation commensurate with experience 12-18 month contract engagement with meaningful technical impact What You'll Be Doing Author and execute
DQ/IQ/OQ/PQ
qualification protocols Own and maintain the detailed expansion project plan (Gantt), including all tasks, owners, dependencies, and milestone dates across validation, qualification, documentation, and equipment workstreams Drive cross-functional teams and contractor deliverables to completion Support GMP documentation including SOPs, MBRs, and validation records Coordinate FAT/SAT activities and manufacturing readiness efforts About You Bachelor's degree in Engineering, Life Sciences, or related field Experience executing equipment qualification in GMP manufacturing Strong knowledge of FDA cGMP regulations and documentation standards Proven ability managing Gantt schedules, risks, and technical project timelines Familiarity with radiopharmaceutical, sterile, or analytical equipment environments preferred How To Apply We'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.

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