Shift Manager, Biopharma Manufacturing

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

Job summary

Bristol Myers Squibb in Devens, MA is seeking a Shift Manager to lead manufacturing unit operations for therapeutic protein production in a cGMP environment. You will train staff, guide troubleshooting, and ensure compliance with quality systems while partnering with Manufacturing Operational Engineering Support for data review and improvements.

The role requires strong knowledge of biologic manufacturing, SOPs/cGMPs, and leadership experience.

Qualifications

BS in science/engineering or related field.
6+ years of biologic manufacturing experience.
Supervisory or leadership experience in a manufacturing setting.
Extensive knowledge of SOPs and cGMPs in a regulated environment.
Experience with pharma/biopharma manufacturing processes and tech transfer.
Strong written and verbal communication skills.

Responsibilities

Oversee execution of manufacturing unit operations (bioreactors, chromatography, media/buffer prep).
Provide on-the-floor training, guidance and problem solving to ensure right-first-time execution.
Lead team development and leverage internal/external relationships to build a strong squad.
Ensure adherence to GMP and SOPs and coordinate day-to-day manufacturing schedule.
Communicate shift updates, conduct huddles, and provide handovers across shifts.
Review critical attributes, oversee equipment checks, and drive process improvements.