Supervisor Quality Control; Overnights

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re hiring a Supervisor of Quality Control for our new highly automated drug substance manufacturing facility in Saratoga Springs. The Supervisor leads a team that completes quality control testing and supports activities for in-process, stability, and final drug products, including utilities, microbiology, sampling, environmental monitoring, and gowning activities.

When

& where:

• Location:

• • Initial:
    Rensselaer, New York, United States
  • Permanent:
    Saratoga Springs, New York, United States

• Work model:
  • Initial: 1st, Mon
    - Fri, 8am-4:30pm
  • Permanent: 12-hour shifts, 7pm-7:30am, alternating 3–4 days per week, including 1 weekend day
  • Transition: candidates must be able to work both schedules. The permanent shift start date will be communicated with reasonable advance notice and is subject to business needs.

Discover your role:

• Hire, onboard, and develop team; define individual development plans tied to technical and leadership competencies
• Set goals, provide ongoing coaching and feedback, and conduct performance reviews; address performance gaps through documented coaching and improvement plans
• Collaborate with Manufacturing, R&D, Formulation, and other support teams to deliver the analytical and Quality Control expertise that keeps production moving
• Provide hands‑on, day‑to‑day oversight of QC activities, supporting your team in real time and driving fast follow‑up and escalation of anything that could affect testing, monitoring, sampling, or manufacturing
• Supervise and perform product testing, utility and environmental monitoring, microbiological testing, sampling, and gowning‑related activities, as applicable.
• Review test reports, QC documentation, and monitoring results to ensure every data point stands up to scrutiny
• Investigates atypical test results as necessary, including results or observations associated with utilities, microbiology, sampling, environmental monitoring, and gowning activities
• Uphold cGMP regulations and SOPs, and take ownership of safety and cGMP performance for direct reports in quality Control Chemistry

This role requires:

• BS/BA in Life Sciences, Chemistry, or Engineering discipline and 5+ years of experience; or an equivalent combination of education and experience
• Previous people leadership/ supervisory experience

Does this sound like you? We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include,

• annual bonuses or other…