Fill/Finish Associate (Internal Fill/Finish MFG)
Regeneron
August 08, 2026
On-site
East Greenbush, NY
Operations
Fill/Finish Associate
Responsibilities:
- Operate highly automated aseptic filling equipment to load drug product into vials, syringes, and cartridges within isolators/cleanroom environments; assemble filled product into syringes and autoinjectors; run packaging lines to label and configure product for distribution.
- Monitor production operations using process controls and feedback systems (pneumatics, robotics, manual checks, PLCs) to ensure throughput, quality, and compliance.
- Perform equipment changeovers, cleaning, handling, and installation of interchangeable parts; maintain clean, safe, inspection-ready workspaces.
- Maintain gowning qualification; adhere to aseptic/cleanroom behaviors; perform environmental monitoring and sampling.
- Create, follow, and improve SOPs/operating procedures aligned with cGMP and regulatory expectations; ensure compliance and escalate nonconformities.
- Record and review GMP data using ALCOA principles; reconcile product/controlled materials; ensure complete training documentation.
- Use electronic systems (MES/eBR, LIMS, training systems, Microsoft Office) for manufacturing operations and documentation.
- Travel domestically and internationally as needed.
Qualifications:
- HS diploma/GED; or AS/BS/BA in Life Sciences or related field.
Benefits:
- Student loan paydown program & tuition reimbursement; family care benefits; inclusion, culture and well-being programs.
Application:
- Apply now ("A Day in the Life" video available).
Responsibilities:
- Operate highly automated aseptic filling equipment to load drug product into vials, syringes, and cartridges within isolators/cleanroom environments; assemble filled product into syringes and autoinjectors; run packaging lines to label and configure product for distribution.
- Monitor production operations using process controls and feedback systems (pneumatics, robotics, manual checks, PLCs) to ensure throughput, quality, and compliance.
- Perform equipment changeovers, cleaning, handling, and installation of interchangeable parts; maintain clean, safe, inspection-ready workspaces.
- Maintain gowning qualification; adhere to aseptic/cleanroom behaviors; perform environmental monitoring and sampling.
- Create, follow, and improve SOPs/operating procedures aligned with cGMP and regulatory expectations; ensure compliance and escalate nonconformities.
- Record and review GMP data using ALCOA principles; reconcile product/controlled materials; ensure complete training documentation.
- Use electronic systems (MES/eBR, LIMS, training systems, Microsoft Office) for manufacturing operations and documentation.
- Travel domestically and internationally as needed.
Qualifications:
- HS diploma/GED; or AS/BS/BA in Life Sciences or related field.
Benefits:
- Student loan paydown program & tuition reimbursement; family care benefits; inclusion, culture and well-being programs.
Application:
- Apply now ("A Day in the Life" video available).