Senior QC Analyst, Cell Therapy - In-Process & Validation

Bristol Myers Squibb; Summit (NJ); On-site; USD 117,372,000 - 141,893,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible Time Off

Job summary

Bristol Myers Squibb is seeking a Senior Specialist, QC Analytical, Cell Therapy to support in-process, final product and stability testing. You will review data, perform method transfer/validation, and assist with deviations and CAPA. The role requires strong technical writing and collaboration in a fast-paced environment.

Shift is Sunday to Wednesday, 1:30pm to 11:30pm, in Summit, NJ. Candidates should have a science degree and 4+ years in a regulated QC setting, with familiarity in cell

Qualifications

• Bachelor's degree or equivalent in science; 4+ years QC experience.
• Experience with cell/molecular biology techniques (cell-based assays, qPCR, ELISA).
• Ability to interpret and apply global regulatory and cGMP requirements.

Responsibilities

• Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
• Troubleshoot and solve problems with minimal guidance.
• Review GMP documentation and perform data verification and data review.
• Revise documents, manage projects, CAPA and deviations/investigations.
• Train and mentor others on QC methods and procedures.

Skills

Problem-solving

Technical writing

Communication

Team collaboration

Education

Bachelor's degree in science

Tools

LIMS

ELN

Lab data systems

Job description

Bristol Myers Squibb is seeking a Senior Specialist, QC Analytical, Cell Therapy to support in-process, final product and stability testing. You will review data, perform method transfer/validation, and assist with deviations and CAPA. The role requires strong technical writing and collaboration in a fast-paced environment.

Shift is Sunday to Wednesday, 1:30pm to 11:30pm, in Summit, NJ. Candidates should have a science degree and 4+ years in a regulated QC setting, with familiarity in cell