Quality Control Analyst

Regeneron Pharmaceuticals • Rensselaer, IN

2d • $25 - $39 • Onsite

About The Position

Regeneron is seeking a Quality Control (QC) Analyst to join its Biochemistry Gels Team in Rensselaer, New York. The role supports the release of lots for market use by performing biochemical analyses on products, in-process materials, and stability samples as part of the company’s quality programs. The position is on-site, first shift, Monday through Friday, 8:00 a.m. to 4:30 p.m.

The analyst supports commercial laboratory testing and helps maintain the processes and systems needed for laboratory operations, including materials, reagents, equipment, electronic systems, documentation, safety, and inspection readiness. The role also includes reviewing results, investigating atypical and out-of-specification outcomes, maintaining GxP compliance, and contributing to process improvement. Depending on the work, the analyst may maintain a project, develop analytical methods, assist with method validation, or support transfer of methods from R&D.

Requirements

• Bachelor of Science or Bachelor of Arts in Life Sciences or a related field, a degree in Biotechnology/Biological Science, or an equivalent combination of education and experience.
• Maintain integrity and honesty.
• Work independently and as part of a team.
• Adapt to a fast-paced setting where priorities may change based on business and patient needs.
• Effective time-management skills to work on multiple projects.
• Strong social skills.
• Excellent written and verbal communication skills.

Responsibilities

• Develop and maintain efficient processes to support commercial testing in laboratory functions.
• Manage or support laboratory materials, reagents, equipment, electronic systems, documents, laboratory safety, and inspection readiness.
• Conduct testing on in-process, product, stability, and/or research samples.
• Complete and/or coordinate laboratory operations activities.
• Ensure timely completion of activities affecting QC commercial operations.
• Review test results for compliance with standards and report quality anomalies.
• Perform laboratory OOT, atypical, and OOS investigations.
• Write and revise control test procedures and SOPs.
• Continuously improve processes while maintaining GxP compliance and keeping tasks on track.
• May maintain a specific project.
• May devise and develop analytical methods and techniques.
• May assist with method validation.
• May help establish transfer of methodology from R&D.

Benefits

• Annual bonuses or other incentive plans may be included, depending on country and role.
• Equity awards may be included, depending on country and role.
• Pension or retirement benefits may be included, depending on country and role.
• 401(k) company match may be included, depending on country and role.
• Health and wellness programs may be included, depending on country and role.
• Fitness centers may be available, depending on country and role.
• Insurance benefits may include medical, dental, vision, life, and disability coverage, depending on country and role.
• Paid time off may be included, depending on country and role.
• Family support benefits may be included, depending on country and role.

What This Job Offers

• Job Type: Full-time