Analytical QC Specialist — Evening Shift (Biotech)

Bristol Myers Squibb

New Jersey

Sur place

USD 72 000 - 88 000

Plein temps

Il y a 7 jours
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Avantages offerts par ce poste

Comprehensive benefits
Flexible work options
Wellbeing support

Résumé du poste

Bristol Myers Squibb is seeking a Quality Control Analyst to perform routine testing of in-process, final product, and stability samples at the Summit, NJ facility. The role supports method transfer, validation, data verification, and GMP documentation within a fast-paced team.

Ideal candidates hold a science degree with 2+ years in analytical QC, experience with cell biology techniques, and the ability to train others while adhering to regulatory standards.

Qualifications

  • Bachelor's degree in science or equivalent required.
  • 2+ years of analytical testing or QC experience in a regulated environment.
  • Experience with cell and molecular biology techniques (cell-based assays, flow cytometry, qPCR, ELISA, aseptic technique).
  • Knowledge of Global Regulatory and cGMP requirements; ability to follow SOPs.
  • Ability to write technical documents and train analysts.

Responsabilités

  • Perform routine testing of in-process, final product, and stability samples.
  • May perform method transfer/validation/verification.
  • Data verification and review of GMP documentation.
  • Document revisions, CAPA, deviations, and investigations; support continuous improvement.
  • Train analysts on general job duties and priorities.

Connaissances

cGMP knowledge
LIMS
ELN
Data verification
Analytical testing
Communication
Technical writing
Team collaboration

Formation

Bachelor's degree in science

Outils

LIMS
ELN

Description du poste

Bristol Myers Squibb is seeking a Quality Control Analyst to perform routine testing of in-process, final product, and stability samples at the Summit, NJ facility. The role supports method transfer, validation, data verification, and GMP documentation within a fast-paced team.

Ideal candidates hold a science degree with 2+ years in analytical QC, experience with cell biology techniques, and the ability to train others while adhering to regulatory standards.

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