Quality Assurance Specialist (Batch Record & Disposition)
Regeneron
August 24, 2026
On-site
East Greenbush, NY
Operations
When & Where
- Location: East Greenbush, New York, United States
- Work model: Monday-Friday, 8am-4:30pm
- Travel percentage: 10% domestic
Discover Your Role
- Represent QA in complex/significant deviations, change controls, CAPAs, including active participation in investigation, evaluation, and problem resolution
- Represent IOPS (Industrial Operations Product Supply) on behalf of QA with external partners; communicate QA policy/procedures and provide input on issues at external sites
- Provide consultation/advice aligned with QA policies
- Perform activities associated with product disposition (e.g., document review, disposition pack preparation, Certificate of Analysis Review)
- Review, edit, or approve Regeneron controlled documents
- Review and approve investigations for raw materials, product, laboratory, facilities, or materials
- Continually evaluate processes/procedures for continuous improvement
- May train and/or mentor junior employees
This Role Requires
- B.S. in life sciences or related field; may substitute proven experience for education
- Associate QA Specialist: 2+ years of experience
- QA Specialist: 4+ years of experience
- Level determined based on experience
Application
- Apply now
- Location: East Greenbush, New York, United States
- Work model: Monday-Friday, 8am-4:30pm
- Travel percentage: 10% domestic
Discover Your Role
- Represent QA in complex/significant deviations, change controls, CAPAs, including active participation in investigation, evaluation, and problem resolution
- Represent IOPS (Industrial Operations Product Supply) on behalf of QA with external partners; communicate QA policy/procedures and provide input on issues at external sites
- Provide consultation/advice aligned with QA policies
- Perform activities associated with product disposition (e.g., document review, disposition pack preparation, Certificate of Analysis Review)
- Review, edit, or approve Regeneron controlled documents
- Review and approve investigations for raw materials, product, laboratory, facilities, or materials
- Continually evaluate processes/procedures for continuous improvement
- May train and/or mentor junior employees
This Role Requires
- B.S. in life sciences or related field; may substitute proven experience for education
- Associate QA Specialist: 2+ years of experience
- QA Specialist: 4+ years of experience
- Level determined based on experience
Application
- Apply now