Analytical QC Analyst — Methods & Compliance

Regeneron Pharmaceuticals, Inc (USA); City of Rensselaer (NY); On-site; USD 52,000 - 84,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

Pension or retirement benefits

401(k) company match

Health and wellness programs

Fitness centers

Insurance benefits (medical, dental, 视

Paid time off

Family support benefits

Job summary

Regeneron Pharmaceuticals, Inc (USA) is seeking a laboratory analyst to perform a variety of chemical or biological analyses on raw materials, in-process materials, products, and stability samples in support of the company’s quality program.

You will gather data, document test results, review outcomes for compliance, and collaborate with internal teams. The role involves maintaining equipment, writing and revising SOPs, and ensuring regulatory requirements are met on-site at our facilities.

Qualifications

• Requires BS/BA in Life Sciences or related field; will substitute relevant experience for education.

Responsibilities

• Gathers data and documents test results.
• Reviews test results to ensure compliance with standards; reports any quality anomalies.
• Complies with all pertinent regulatory agency requirements.
• Participates in required training activities.
• Maintains laboratory supplies.
• Conducts testing on raw materials, in-process, product, stability, and/or research samples.
• Writes and revises control test procedures and SOPs.
• Completes test records and reviews data.
• Calibrates or verifies calibration of instruments/devices prior to use.
• Interacts with outside customers or functional peer groups.
• May be responsible for maintaining a specific project.
• May devise or develop new analytical methods and techniques.
• May assist in validation of methods.
• May be involved in establishing the transfer of methodology from R&D.

Education

BS/BA in Life Sciences or related field

Job description

Regeneron Pharmaceuticals, Inc (USA) is seeking a laboratory analyst to perform a variety of chemical or biological analyses on raw materials, in-process materials, products, and stability samples in support of the company’s quality program.

You will gather data, document test results, review outcomes for compliance, and collaborate with internal teams. The role involves maintaining equipment, writing and revising SOPs, and ensuring regulatory requirements are met on-site at our facilities.