QC Analytical Scientist

Bristol Myers Squibb EU Policy

West Summit (UT)

On-site

USD 34,000 - 58,000

Full time

5 days ago
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Benefits offered by this job

Flexible Time Off
11 paid company holidays
Paid vacation

Job summary

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support in-process, final product, and stability testing, with data review and verification responsibilities. The role includes potential method transfer, deviations, investigations, and continuous improvement initiatives.

Shift: Wed – Sat, 1:30pm – 11:30pm. Reporting to QC management, you will collaborate with cross-functional teams to ensure quality and compliance in a fast-paced environment.

Qualifications

  • Bachelor's degree or equivalent required, preferably in science.
  • Demonstrated 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).

Responsibilities

  • Perform routine testing of in-process, final product, and stability samples.
  • Perform testing for method transfer/validation/verification.
  • Perform data verification, data review and review of GMP documentation for general methods.
  • May perform document revision, CAPA and deviation/investigation tasks and continuous improvement efforts.
  • Train analysts on general job duties.
  • Perform other tasks as assigned.

Skills

cGMP knowledge or interpretation
LIMS/ELN knowledge
Problem-solving
Effective communication
Technical writing
Teamwork under pressure

Education

Bachelor's degree in science
2+ years QC/analytical testing
Cell & molecular biology techniques

Tools

LIMS
ELN

Job description

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support in-process, final product, and stability testing, with data review and verification responsibilities. The role includes potential method transfer, deviations, investigations, and continuous improvement initiatives.

Shift: Wed – Sat, 1:30pm – 11:30pm. Reporting to QC management, you will collaborate with cross-functional teams to ensure quality and compliance in a fast-paced environment.

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