QC Analytical Specialist — In-Process & Final Product

Bristol Myers Squibb; Summit (NJ); On-site; USD 4,822,000 - 5,786,000; Full time

Benefits offered by this job

Flexible Time Off (FTO)

11 paid holidays per year

Company benefits package

Paid vacation for new hires

Job summary

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support testing of in-process, final product and stability samples. You will assist with method transfers and data verification, and contribute to investigations and CAPAs within a GMP environment.

The role requires strong knowledge of regulatory requirements, data systems, and teamwork. Shift: Wed–Sat, 1:30pm–11:30pm, based in Summit, NJ with full benefits and growth opportunities.

Qualifications

• Bachelor's degree in science preferred
• 2+ years of QC analytical testing experience
• Experience with cell/molecular biology techniques (e.g., flow cytometry, qPCR, ELISA) preferred

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• Perform testing for method transfer/validation/verification.
• Data verification and GMP documentation review.
• Assist with deviations, investigations and continuous improvement efforts.

Skills

GxP compliance

LIMS/ELN experience

Data verification

Technical writing

Team collaboration

Problem solving

Education

Science degree

2+ years QC experience

Cell/molecular biology techniques

Tools

LIMS

ELN

Job description

Bristol Myers Squibb is seeking a Specialist, QC Analytical to support testing of in-process, final product and stability samples. You will assist with method transfers and data verification, and contribute to investigations and CAPAs within a GMP environment.

The role requires strong knowledge of regulatory requirements, data systems, and teamwork. Shift: Wed–Sat, 1:30pm–11:30pm, based in Summit, NJ with full benefits and growth opportunities.