External Manufacturing Specialist, Advanced Therapies
Regeneron · Tech Valley
CMCFull-time$62k–$110kCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
What they're looking for
- Bachelor's degree in scientific field plus 0-2 years cGMP manufacturing experience
- Experience with synthetic processes, small molecule synthesis, antibodies, or fermentation
- Knowledge of bulk manufacturing techniques including fermentation and purification
- Understanding of cGMP, FDA regulations, ICH and EU regulatory frameworks
- Strong written and oral communication skills
- Ability to work independently with minimal supervision toward established goals
- Adaptability and resilience in dynamic operational environments
What you'll be doing
- Serve as operational contact for contract manufacturing sites managing day-to-day activities
- Coordinate external manufacturing including batch scheduling, material supply, and cycle time tracking
- Act as liaison between Regeneron departments and contract manufacturers on operational matters
- Monitor cGMP compliance at contract manufacturers and support investigations
- Review pre-production and executed batch records for accuracy and completeness
Privacy & handoff
This role links to Regeneron's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.