Evening Cell Therapy QC Analyst

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

Benefits offered by this job

Flexible Time Off

11 paid holidays

Vacation time

Stock options

Job summary

Bristol-Myers Squibb Company in Summit, NJ is seeking a Specialist, QC Analytical (Cell Therapy) to support in-process, final product and stability testing, including data review and verification. The role involves method transfer, deviations, investigations and participation in continuous improvement.

You will work Wed–Sat, 1:30pm–11:30pm, perform routine testing, data verification, GMP document review, and assist with training and cross-functional projects.

Qualifications

• Bachelor's degree or equivalent required, preferably in science.
• 2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience.
• Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and 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, project, CAPA and deviation/investigation related tasks and/ or continuous improvement efforts.
• Train analysts on general job duties.
• Perform other tasks as assigned.

Skills

cGMP knowledge

Data review/verification

LIMS experience

ELN experience

Communication skills

Training analysts

Education

Bachelor's degree or equivalent

Tools

LIMS

ELN

Job description

Bristol-Myers Squibb Company in Summit, NJ is seeking a Specialist, QC Analytical (Cell Therapy) to support in-process, final product and stability testing, including data review and verification. The role involves method transfer, deviations, investigations and participation in continuous improvement.

You will work Wed–Sat, 1:30pm–11:30pm, perform routine testing, data verification, GMP document review, and assist with training and cross-functional projects.