Quality Control Analyst

Regeneron Pharmaceuticals • Saratoga Springs, UT

7d • $25 - $44 • Onsite

About The Position

Regeneron is hiring multiple Quality Control Analysts for its highly automated drug substance manufacturing facility. The role performs chemical, biological, or microbial analyses and sampling of raw materials, products, in-process materials, utilities, environmental monitoring, and stability or research samples in support of the company’s quality program. The role begins on-site in Rensselaer, New York, and later transitions to on-site work in Saratoga Springs, New York. 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 level offered will be determined based on experience.

The initial schedule is full time, Monday through Friday, 8:00 a.m. to 4:30 p.m. The permanent schedule consists of rotating 12-hour shifts, 7:00 a.m. to 7:30 p.m., three to four days per week, including one weekend day. The position requires cleanroom work and full cleanroom attire, with the ability to perform physical requirements for the entirety of shifts, up to 10 hours in a cleanroom environment.

The role requires a B.S. in Life Sciences or a related field, or an equivalent combination of education and experience. Regeneron offers a competitive total rewards package that may vary by country and role. The listed hourly salary range is $24.76–$44.42.

Requirements

• B.S. in Life Sciences or a related field, or an equivalent combination of education and experience.
• Candidates must be able to work both the initial and permanent schedules.
• Associate Quality Control Analyst: 0–2 years of experience.
• Quality Control Analyst: 2+ years of experience.
• Senior Quality Control Analyst I: 4+ years of experience.
• Ability to perform the physical requirements of the role for the entirety of a shift, up to 10 hours in a cleanroom environment.
• Ability to wear full cleanroom attire and remove jewelry, makeup, and nail adornments while wearing it.
• Ability to perform physical activities that may include bending, climbing, crawling, kneeling, reaching, overhead reaching, sitting, squatting, walking, standing, driving, and hand manipulation.
• Ability to lift, push, or pull up to 50 pounds.

Responsibilities

• Gather data and document test results.
• Review test results for compliance with standards and report quality anomalies.
• Comply with pertinent regulatory agency requirements.
• Participate in required GMP training activities.
• Maintain laboratory supplies.
• Conduct testing and sampling on raw materials, in-process materials, products, stability samples, and/or research samples.
• Write and revise control test procedures and standard operating procedures (SOPs).
• Complete test records and review data.
• Calibrate instruments and devices, or verify their calibration, prior to use.
• Interact with outside customers or functional peer groups.
• Participate in projects aligned with the company’s scientific initiatives.
• Devise or develop analytical methods and techniques.
• Assist in method validation.
• Partner with internal teams to establish the transfer of methodology from R&D.

Benefits

• Student loan paydown program
• Tuition reimbursement
• Family care benefits
• Relocation assistance
• Inclusion, culture, and well-being programs, including physical and mental health programs
• Potential annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, medical, dental, vision, life and disability insurance, paid time off, and family support benefits

What This Job Offers

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