QC Specialist
RegeneronCambridge, Massachusetts, United States
Posted April 14, 2026
71800 - 116800 USD
Full Time
About the Company
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.
Job Description
Our QC Specialist supports Phase 1 GMP testing laboratory for release and stability for multiple stages of our cell and gene therapy products. They perform analytical methods, data review and trending, and interface with Analytical Development and Method Validation. They have a cGMP operational and technical background in cell biology, biochemistry and/or molecular biology.
Requirements
- BS in Biotechnology discipline
- 2+ years experience in cGMP/GxP environment
- Hands on experience in cell culture, flow cytometry, quantitative PCR, and other bioanalytical methods, such as ELISA
- Superb organizational, analytical, and communications skills and 'do-what-it-takes' attitude
- Strong capacity to learn and receptive to change
- Self-directed individual who is able to work with limited direction in a fast-paced, goal-oriented environment
Benefits
- health and wellness programs (including medical, dental, vision, life, and disability insurance)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental leave)
