Biologics Manufacturing Technology Scientist

Bristol Myers Squibb; Harvard (MA); On-site; USD 88,000 - 107,000; Full time

Job summary

Bristol Myers Squibb is seeking an Associate Scientist/Engineer in Manufacturing Technology at the Devens, MA site. You will act as a process technical expert for large-scale cell culture and single-use manufacturing, driving deviations investigations, CAPA, and ongoing improvements to ensure GMP compliance and reliable production of life-changing therapies.

You will collaborate with Manufacturing, Quality, Validation, Analytical, and Technical Product Teams to advance process robustness, tech

Qualifications

• Bachelor’s degree in engineering, life sciences, biochemistry, biotechnology or related field; typically 3–5 years in biopharma manufacturing.
• Working knowledge of commercial biologics manufacturing, upstream/downstream unit ops, GMP.
• Familiarity with SOPs, cGMPs, quality systems and regulatory expectations in manufacturing.

Responsibilities

• Provide technical support for commercial biologics manufacturing operations, including deviation troubleshooting and process robustness improvements.
• Lead/root-cause investigations for deviations with data review, risk assessments and CAPA development.
• Support regulatory inspections and health authority responses with inspection-ready documentation.
• Provide on-call technical support for 24x7 large-scale cell culture operations as needed.
• Contribute to technology transfer, validation, and lifecycle management activities across teams.

Skills

Cross-functional collaboration

Analytical problem-solving

Written communication

Education

Bachelor's degree in engineering, life sciences, biotechnology or related field

Tools

CAPA systems

Job description

Bristol Myers Squibb is seeking an Associate Scientist/Engineer in Manufacturing Technology at the Devens, MA site. You will act as a process technical expert for large-scale cell culture and single-use manufacturing, driving deviations investigations, CAPA, and ongoing improvements to ensure GMP compliance and reliable production of life-changing therapies.

You will collaborate with Manufacturing, Quality, Validation, Analytical, and Technical Product Teams to advance process robustness, tech