Quality Control Analyst (Overnights)

Regeneron Pharmaceuticals•Saratoga Springs, UT
•$25 - $44•Onsite

About The Position

Regeneron is hiring multiple Quality Control Analysts to support its quality program at a highly automated drug substance manufacturing facility. The role involves performing chemical, biological, or microbial analyses and sampling of raw materials, products, in-process materials, utilities, environmental monitoring, or stability samples. The position begins onsite in Rensselaer, New York, on a weekday first shift, and transitions to onsite work in Saratoga Springs, New York, on rotating overnight 12-hour shifts. Candidates must be able to work both schedules; the permanent shift start date will be communicated with reasonable advance notice and depends on business needs. The level at hire will be determined based on experience.

Requirements

  • Bachelor of Science in Life Sciences or a related field, or an equivalent combination of education and experience.
  • Associate Quality Control Analyst level: 0–2 years of experience.
  • Quality Control Analyst level: 2 or more years of experience.
  • Senior Quality Control Analyst I level: 4 or more years of experience.
  • Ability to work both the initial and permanent schedules.
  • Ability to wear full cleanroom attire and remove jewelry, makeup, and nail adornments while wearing it.
  • 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 perform physical activities that may include bending, climbing, crawling, kneeling, reaching, overhead reaching, sitting, squatting, walking, standing, driving, and hand manipulation, and 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 applicable regulatory agency requirements.
  • Participate in required GMP training.
  • 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.
  • Complete test records and review data.
  • Calibrate instruments and devices, or verify their calibration, before use.
  • Interact with external customers and functional peer groups.
  • Participate in projects aligned with scientific initiatives.
  • Devise or develop analytical methods and techniques.
  • Assist with method validation.
  • Partner with internal teams to establish 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
  • Competitive 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, medical, dental, vision, life and disability insurance, paid time off, and family support benefits
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