What are the responsibilities and job description for the Project Manager & Validation Specialist position at Scientific Search?
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
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.
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
- 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
- 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
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.