Virology QC Associate — cGMP Lab & Data Reporting

Regeneron Pharmaceuticals, Inc.; United States; On-site; USD 30,000 - 47,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks an Associate Quality Control Virology Analyst to support virus and mycoplasma testing in a cGMP environment at our East Greenbush, NY site.

You will manage sample custody, processing, testing and data reporting to ensure accuracy and compliance. Responsibilities include data review, trend analysis, and participating in investigations, with on-site work Monday–Friday, 8:00am–4:30pm.

Qualifications

• BS/BA in Cell Biology, Microbiology, Biochemistry or related science.
• Experience in GMP virology or cell culture lab preferred.
• Ability to collect, enter data and generate reports from electronic systems.

Responsibilities

• Ensure proper level of laboratory supplies and reagents and maintain audit readiness and cGMP compliant.
• Perform routine and non-routine virus and mycoplasma testing of products per cGMP SOPs.
• Review data for conformance to cGMP and specifications; assist with investigations.
• Collect, process and report data for in-process testing for clinical/commercial facilities.
• Apply basic and advanced troubleshooting methods.
• Serve as SME for an assigned assay.
• Assist in data trending, review, and lab maintenance.
• Participate in non-routine projects and investigations as needed.

Skills

Cell culture

Data reporting

cGMP compliance

Virus testing

Education

BS/BA in Cell Biology, Microbiology, Biochemistry

Job description

Regeneron Pharmaceuticals, Inc. seeks an Associate Quality Control Virology Analyst to support virus and mycoplasma testing in a cGMP environment at our East Greenbush, NY site.

You will manage sample custody, processing, testing and data reporting to ensure accuracy and compliance. Responsibilities include data review, trend analysis, and participating in investigations, with on-site work Monday–Friday, 8:00am–4:30pm.