Cell Therapy QC Associate: In-Process & Final Product

Bristol-Myers Squibb Co; Harvard (MA); On-site; USD 51,000 - 62,000; Full time

Job summary

Bristol Myers Squibb Co. is seeking an Associate, QC Analytical for its Devens, MA site. You will support QC testing across in-process, final product, and stability samples, and assist with documentation and investigations in a fast-paced environment.

The role requires 0-2+ years in analytical testing or QC, familiarity with GMP documentation, and the ability to work as part of a team. Full-time, on-site schedule is provided with comprehensive benefits.

Qualifications

• Bachelor's degree preferred in science.
• 0-2+ years of relevant analytical testing or QC experience or equivalent.
• Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
• Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.

Responsibilities

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

Skills

Follow procedures

Analytical testing basics

Communication

Attention to detail

Team collaboration

Education

Bachelor's degree in science

Job description

Bristol Myers Squibb Co. is seeking an Associate, QC Analytical for its Devens, MA site. You will support QC testing across in-process, final product, and stability samples, and assist with documentation and investigations in a fast-paced environment.

The role requires 0-2+ years in analytical testing or QC, familiarity with GMP documentation, and the ability to work as part of a team. Full-time, on-site schedule is provided with comprehensive benefits.