QC Analytical Molecular Associate — In-Process & Stability Testing

Biopharma Careers; Harvard (MA); On-site; USD 50,000 - 62,000; Full time

Benefits offered by this job

Health Coverage

Wellbeing Programs

401(k) plan

Job summary

Bristol Myers Squibb is seeking a QC Analyst to support in-process, final product, and stability testing. The role includes assisting with documentation, deviations, investigations, and continuous improvement while working a Wed-Sat night shift in Devens, MA.

Ideal candidates have 0-2+ years in analytical QC in a regulated setting, strong attention to detail, and ability to follow procedures with clear communication in a fast-paced team environment.

Qualifications

• Bachelor's degree preferred in science; Associate’s degree with equivalent education may be considered.
• 0-2+ years of relevant analytical testing or QC experience in a regulated environment.
• Demonstrated experience with basic laboratory techniques and laboratory safety practices.

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.

Skills

Procedures compliance

Analytical testing

Communication

Attention to detail

Teamwork

Education

Bachelor's degree in science

Associate’s degree equivalent

Job description

Bristol Myers Squibb is seeking a QC Analyst to support in-process, final product, and stability testing. The role includes assisting with documentation, deviations, investigations, and continuous improvement while working a Wed-Sat night shift in Devens, MA.

Ideal candidates have 0-2+ years in analytical QC in a regulated setting, strong attention to detail, and ability to follow procedures with clear communication in a fast-paced team environment.