Night Shift Lead, Cell Therapy Manufacturing

Bristol Myers Squibb EU Policy; Harvard (MA); On-site; USD 55,000 - 67,000; Full time

Benefits offered by this job

Flexible Time Off (FTO)

11 paid holidays

Comprehensive benefits package

Retirement and financial protection

Job summary

Bristol Myers Squibb in Devens, MA, is seeking a Night Shift Specialist, Lead Manufacturing Associate, to execute cell therapy manufacturing tasks on a rotational night schedule. You will work within cleanroom GMP environments, following SOPs and batch records to ensure compliant production and safe handling of materials.

The role requires a 4+ year background in cGMP bioprocessing or related fields, a science/engineering degree, and ability to work in a team across shifts.

Qualifications

• Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.
• Ability to work assigned shift (including nights, holidays, weekends).
• Cleanroom environment and aseptic processing capability.
• Comfort with exposure to human blood components.
• Able to be near magnets during manufacturing processes.
• Experience in cell therapy manufacturing and related equipment.

Responsibilities

• Execute operations per SOPs and batch records.
• Set up manufacturing areas and equipment; assist in commissioning.
• Support investigations and problem solving in cross-functional teams.
• Train others on SOPs and work instructions for manufacturing tasks.
• Collaborate with production planning to meet daily schedule.

Skills

cGMP knowledge

Cleanroom aseptic

Biologics/cell therapy

Shift flexibility

Blood exposure safety

Magnet proximity awareness

Team collaboration

Education

Bachelor's degree in science/engineering

Job description

Bristol Myers Squibb in Devens, MA, is seeking a Night Shift Specialist, Lead Manufacturing Associate, to execute cell therapy manufacturing tasks on a rotational night schedule. You will work within cleanroom GMP environments, following SOPs and batch records to ensure compliant production and safe handling of materials.

The role requires a 4+ year background in cGMP bioprocessing or related fields, a science/engineering degree, and ability to work in a team across shifts.