Supervisor Quality Control (Overnights)

Regeneron Pharmaceuticals • Saratoga Springs, UT

5d • $80,300 - $131,300 • Onsite

About The Position

Regeneron is hiring a Supervisor of Quality Control for its new highly automated drug substance manufacturing facility in Saratoga Springs. The supervisor leads a team responsible for quality control testing and support activities for in-process, stability, and final drug products, including utilities, microbiology, sampling, environmental monitoring, and gowning.

The role initially works in Rensselaer, New York, on a Monday–Friday, 8:00 a.m.–4:30 p.m. schedule. The permanent location is Saratoga Springs, New York, with 12-hour shifts from 7:00 p.m.–7:30 a.m., alternating three or four days per week and including one weekend day. 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.

The supervisor hires, develops, and oversees team members; collaborates with manufacturing and support groups; provides hands-on oversight of QC work; reviews testing and monitoring documentation; investigates atypical results; and upholds cGMP, SOP, and safety expectations.

Requirements

• Bachelor of Science or Bachelor of Arts in Life Sciences, Chemistry, or an Engineering discipline and at least 5 years of experience, or an equivalent combination of education and experience.
• Previous people leadership or supervisory experience.
• Ability to work both the initial Monday–Friday, 8:00 a.m.–4:30 p.m. schedule and the permanent 12-hour overnight schedule, including one weekend day.

Responsibilities

• Hire, onboard, and develop team members, and define individual development plans tied to technical and leadership competencies.
• Set goals, provide ongoing coaching and feedback, conduct performance reviews, and address performance gaps through documented coaching and improvement plans.
• Collaborate with Manufacturing, R&D, Formulation, and other support teams to provide analytical and Quality Control expertise that supports production.
• Provide hands-on, day-to-day oversight of QC activities, support the team in real time, and ensure fast follow-up and escalation of issues 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 data are reliable and meet scrutiny.
• Investigate atypical test results and relevant 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.

Benefits

• Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits, paid time off, and family support benefits.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager