Biopharma Manufacturing Shift Lead — Single-Use Facility

Bristol Myers Squibb EU Policy

Harvard (MA)

On-site

USD 105,000 - 127,000

Full time

3 days ago
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Benefits offered by this job

Health Coverage
Wellbeing Programs
401(k) plan
Disability & Life Insurance

Job summary

Bristol Myers Squibb is seeking a Shift Manager to lead manufacturing of therapeutic proteins, ensuring compliant operations and a culture of continuous improvement. You will supervise a team, guide troubleshooting, and drive data-driven decisions on the floor in a cGMP environment.

The role emphasizes on-time execution, training, and collaboration with support groups to maintain quality and productivity.

Qualifications

  • B.S. in science/engineering/biochemistry or related field.
  • 6+ years biologic manufacturing experience; leadership preferred.
  • Strong knowledge of SOPs and cGMPs in regulated env.
  • Experience with pharma tech transfer and process development.
  • Adaptable to fast-paced, changing business environment.
  • Effective communication and technical writing skills.

Responsibilities

  • Oversee execution of manufacturing unit operations (bioreactors, chromatography, media/buffer prep).
  • Drive right first time (RFT) execution with on-floor training and guidance.
  • Develop and mentor the team; build a high-performing unit.
  • Ensure adherence to GMPs and SOPs across the shift.
  • Coordinate daily manufacturing schedule and shift handovers.
  • Lead investigations and drive process improvements.

Skills

BS in science/engineering
Biologic manufacturing exp
Leadership / supervision
SOPs & cGMPs
Pharma manufacturing
Communication & writing

Education

BS in science/engineering/biochemistry

Tools

SAP
DeltaV
Syncade
OSI/Pi Historian
Veeva Vault
Maximo

Job description

Bristol Myers Squibb is seeking a Shift Manager to lead manufacturing of therapeutic proteins, ensuring compliant operations and a culture of continuous improvement. You will supervise a team, guide troubleshooting, and drive data-driven decisions on the floor in a cGMP environment.

The role emphasizes on-time execution, training, and collaboration with support groups to maintain quality and productivity.

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