Cell Therapy QC Analyst In-Process & Final Product

Bristol-Myers Squibb Co; Summit (NJ); On-site; USD 48,000 - 58,000; Full time

Benefits offered by this job

Comprehensive benefits package

Flexible Time Off (FTO)

Paid holidays

Job summary

Bristol-Myers Squibb Co. is seeking a Specialist, QC Analytical, Cell Therapy for Summit, NJ. The role supports in-process, final product, and stability testing with data review and potential method transfers. Responsibilities include GMP documentation review and continuous improvement efforts.

Shift: Wed–Sat, 1:30pm–11:30pm. Requires a science degree and 2+ years of QC experience with strong data interpretation and problem-solving abilities.

Qualifications

• Bachelor's degree or equivalent required, preferably in science.
• 2+ years of relevant analytical testing or QC experience or equivalent.

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, project, CAPA and deviation/investigation related tasks.
• Train analysts on general job duties.
• Perform other tasks as assigned.

Skills

GMP knowledge

LIMS

ELN

data review

problem solving

communication

technical writing

Education

Bachelor's degree or equivalent

2+ years QC experience

Tools

LIMS

ELN

Job description

Bristol-Myers Squibb Co. is seeking a Specialist, QC Analytical, Cell Therapy for Summit, NJ. The role supports in-process, final product, and stability testing with data review and potential method transfers. Responsibilities include GMP documentation review and continuous improvement efforts.

Shift: Wed–Sat, 1:30pm–11:30pm. Requires a science degree and 2+ years of QC experience with strong data interpretation and problem-solving abilities.