Director, Internal Manufacturing
$172,000–$287,000 year
On-site · Springfield, New Jersey, United States
Job Summary
Director, Internal Manufacturing leads Evergreen Manufacturing Operations for radiopharmaceutical manufacturing (RLT, PET, isotope products), providing technical leadership to ensure safe, compliant, and reliable end-to-end production from design and tech transfer to routine commercial execution and continuous improvement. The role ensures full cGMP compliance with applicable regulations, partners across Quality, Engineering, Employee Health and Safety, Radiation Safety, Supply Chain, and Regulatory, and focuses on capability, capacity, and operational excellence. Responsibilities include establishing and monitoring operational metrics, contributing to site/network strategy, maintaining deep radiopharmaceutical technical expertise, leading capital projects, supporting regulatory interactions and inspections, fostering a culture of safety and continuous improvement, and developing technical talent while maintaining robust Quality and issue management systems. The position requires on-site presence in New Jersey five days a week, with eligibility to work for any employer within the United States.},
Required Qualifications
- Bachelor’s degree in chemistry, Chemical Engineering, Pharmaceutical Sciences, Biology, or related scientific/technical discipline (or equivalent experience)
- 10+ years of experience in radiopharmaceutical, sterile, or biologics/pharmaceutical GMP manufacturing, including direct experience with radiochemistry/radiosynthesis operations and/or aseptic processing in a regulated environment
- Experience with Operational Excellence/Lean methodologies and structured problem solving
- Working knowledge of GMP documentation systems and quality processes (deviation management, change control, investigations, CAPA, batch record review/release)
- Experience supporting/leading qualification/validation activities and process validation/continued process verification in a GMP environment
- Proven ability to lead technical discussions with Quality and regulators/auditors, including inspection readiness and clear written responses
- Demonstrated ability to lead, coach, and influence cross-functional teams
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.