Reference Standards QC Analyst — On-Site Lab Impact

Regeneron Pharmaceuticals, Inc.; New York (NY); On-site; USD 34,000 - 54,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Quality Control Analyst (Reference Standards) to manage the lifecycle of reference standards and materials, ensuring data is gathered, results reviewed for compliance, and instruments are calibrated prior to use.

The role involves writing and revising SOPs, supporting regulatory requirements, and collaborating with cross-functional teams to maintain laboratory readiness and accuracy across programs.

Qualifications

• Requires BS/BA in Life Sciences or related field; relevant experience may substitute education.
• Experience with reference standards and quality control is preferred.

Responsibilities

• Manage life-cycle of reference standards and reference materials.
• Gather data and document test results.
• Review results for compliance with standards; report quality anomalies.
• Calibrate or verify calibration of instruments prior to use.
• Write and revise control test procedures and SOPs.
• Interact with outside customers or functional peer groups.

Skills

Life sciences

Quality control

Documentation

SOPs

Education

BS/BA in Life Sciences

Tools

Laboratory instruments

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Quality Control Analyst (Reference Standards) to manage the lifecycle of reference standards and materials, ensuring data is gathered, results reviewed for compliance, and instruments are calibrated prior to use.

The role involves writing and revising SOPs, supporting regulatory requirements, and collaborating with cross-functional teams to maintain laboratory readiness and accuracy across programs.