Biomanufacturing Shift Lead, Single-Use Facility

Biopharma Careers; Harvard (MA); On-site; USD 105,000 - 127,000; Full time

Benefits offered by this job

Health Coverage

401(k) plan

Paid Time Off

Stock options

Job summary

Bristol Myers Squibb in Devens, MA is seeking a Shift Manager to lead commercial manufacturing processes for therapeutic proteins with emphasis on cGMP compliance and efficient production on the floor. You will train and develop a team, coordinate with cross-functional groups, and drive safety, quality, and continuous improvement, focusing on right-first-time execution.

Applicants should have strong leadership, manufacturing experience, and knowledge of GMP processes, with a track record of

Qualifications

• BS in science/engineering or related discipline; highly desired.
• 6+ years of biologic manufacturing experience; supervisory/leadership experience.
• Extensive knowledge of SOPs and cGMPs in a regulatory environment.
• Knowledge of pharmaceutical/biopharmaceutical manufacturing processes.
• Able to adapt to a fast-paced, changing environment.

Responsibilities

• Oversee execution of manufacturing unit operations on the floor.
• Provide training, guidance, and real-time problem solving to ensure right-first-time execution.
• Lead team development and cross-functional collaboration.
• Ensure adherence to cGMPs and SOPs; manage scheduling and communications.
• Coordinate with support groups to review data and drive improvements.

Skills

B.S. in science/engineering

6+ years manufacturing experience

Supervisory/leadership

cGMP/SOP knowledge

Technical communication

Education

B.S. in science/engineering/biochemistry

Tools

DeltaV

OSI/Pi Historian

SAP

Veeva Vault

Maximo

Job description

Bristol Myers Squibb in Devens, MA is seeking a Shift Manager to lead commercial manufacturing processes for therapeutic proteins with emphasis on cGMP compliance and efficient production on the floor. You will train and develop a team, coordinate with cross-functional groups, and drive safety, quality, and continuous improvement, focusing on right-first-time execution.

Applicants should have strong leadership, manufacturing experience, and knowledge of GMP processes, with a track record of