Virology QC Analyst: Data, Testing & Compliance

Regeneron Pharmaceuticals, Inc.

Town of East Greenbush (NY)

Presencial

USD 30 000 - 47 000

Tempo integral

há 42 horas
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Resumo da oferta

Regeneron Pharmaceuticals, Inc. is seeking an Associate Quality Control Virology Analyst in East Greenbush, NY.

In this role you will manage sample chain of custody, sample processing, testing and test data reporting and archival. You will maintain an audit-ready laboratory with cGMP compliance, perform routine virus and mycoplasma testing, review data for specification conformance, collect and report in-process testing data, and serve as SME for an assigned assay.

Qualificações

  • BS/BA in Cell Biology, Microbiology, Biochemistry or related science.
  • GMP virology or cell culture lab experience preferred.
  • Strong attention to detail in a regulated environment.

Responsabilidades

  • Maintain sample chain of custody, processing, testing and data reporting.
  • Ensure audit-ready lab and cGMP compliance at all times.
  • Review data for conformance to specifications and investigate deviations.
  • Collect and report data for in-process testing for clinical/commercial facilities.
  • Apply troubleshooting methods and serve as SME for an assigned assay.
  • Assist in data trending, data review, and lab maintenance activities.
  • Support studies and protocols; perform cell culture to support virus testing.
  • Enter data and generate reports from electronic systems; ensure GMP/GLP practices.

Conhecimentos

Cell culture
Virus testing
Data reporting
cGMP compliance

Formação académica

BS/BA in Cell Biology, Microbiology, Biochemistry

Ferramentas

Electronic systems

Descrição da oferta de emprego

Regeneron Pharmaceuticals, Inc. is seeking an Associate Quality Control Virology Analyst in East Greenbush, NY.

In this role you will manage sample chain of custody, sample processing, testing and test data reporting and archival. You will maintain an audit-ready laboratory with cGMP compliance, perform routine virus and mycoplasma testing, review data for specification conformance, collect and report in-process testing data, and serve as SME for an assigned assay.

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