Fill/Finish Associate (Internal Fill/Finish MFG)
Regeneron
August 19, 2026
On-site
East Greenbush, NY
Operations
Responsibilities:
- Operate highly automated aseptic filling equipment to load drug product into vials, syringes, and cartridges; assemble filled product into syringes and autoinjectors; and run packaging lines to label/configure product for distribution.
- Monitor production 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; follow aseptic/cleanroom behaviors; perform environmental monitoring and sampling.
- Create, follow, and improve SOPs/operating procedures aligned with cGMP; ensure compliance and promptly escalate nonconformities.
- Record/review GMP data using ALCOA principles; reconcile product/controlled materials; ensure training documentation is complete.
- Use electronic systems (e.g., MES/eBR, LIMS, training systems, Microsoft Office) to support manufacturing operations.
- Travel domestically/internationally as needed.
Qualifications/Required:
- HS diploma or GED.
Preferred:
- AS/BS/BA in Life Sciences or related field.
Skills/Knowledge:
- Aseptic/cleanroom practices; cGMP documentation and ALCOA data integrity; ability to work up to 10 hours in a cleanroom environment and perform physical tasks (including lifting/pushing/pulling up to 50 lbs).
Benefits (if offered):
- Student loan paydown program & tuition reimbursement; family care benefits; inclusion, culture and well-being programs (physical & mental health).
Application:
- Apply now.
- Operate highly automated aseptic filling equipment to load drug product into vials, syringes, and cartridges; assemble filled product into syringes and autoinjectors; and run packaging lines to label/configure product for distribution.
- Monitor production 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; follow aseptic/cleanroom behaviors; perform environmental monitoring and sampling.
- Create, follow, and improve SOPs/operating procedures aligned with cGMP; ensure compliance and promptly escalate nonconformities.
- Record/review GMP data using ALCOA principles; reconcile product/controlled materials; ensure training documentation is complete.
- Use electronic systems (e.g., MES/eBR, LIMS, training systems, Microsoft Office) to support manufacturing operations.
- Travel domestically/internationally as needed.
Qualifications/Required:
- HS diploma or GED.
Preferred:
- AS/BS/BA in Life Sciences or related field.
Skills/Knowledge:
- Aseptic/cleanroom practices; cGMP documentation and ALCOA data integrity; ability to work up to 10 hours in a cleanroom environment and perform physical tasks (including lifting/pushing/pulling up to 50 lbs).
Benefits (if offered):
- Student loan paydown program & tuition reimbursement; family care benefits; inclusion, culture and well-being programs (physical & mental health).
Application:
- Apply now.