QC Analytical Associate, Cell Therapy Manufacturing

Bristol-Myers Squibb Co

Summit (NJ)

In loco

USD 47.000 - 58.000

Tempo pieno

4 giorni fa
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Descrizione del lavoro

Bristol Myers Squibb is seeking an Associate for QC Analytical in Summit, NJ to perform testing of in-process, final product, and stability samples in accordance with cGMP requirements. The role may include data verification and GMP documentation review, supporting CAPA and deviations, and training analysts as needed.

The position reports to the Manager or Senior Manager, QC Analytical and requires a Bachelor’s (preferred) or equivalent with 0-2+ years in analytical QC within a regulated

Competenze

  • Bachelor's degree preferred in science.
  • Associates degree with equivalent combination of education and work experience may be considered.
  • 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
  • Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
  • Prior experience in cell and molecular biology techniques (e.g., cell based assays, flow cytometry, qPCR, aseptic technique) is preferred.

Mansioni

  • Perform routine testing of in-process, final product, and stability samples.
  • May review GMP documentation and perform data verification.
  • Support document revision, project, CAPA and deviation/investigation related tasks and/ or continuous improvement efforts.
  • May train analysts on general job duties.
  • Perform other tasks as assigned.

Descrizione del lavoro

Bristol Myers Squibb is seeking an Associate for QC Analytical in Summit, NJ to perform testing of in-process, final product, and stability samples in accordance with cGMP requirements. The role may include data verification and GMP documentation review, supporting CAPA and deviations, and training analysts as needed.

The position reports to the Manager or Senior Manager, QC Analytical and requires a Bachelor’s (preferred) or equivalent with 0-2+ years in analytical QC within a regulated

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