Senior Bioprocess Manufacturing Lead

Bristol Myers Squibb; Harvard (MA); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Comprehensive benefits

Job summary

Bristol Myers Squibb in the United States is seeking a Technical Lead to serve as the shift's technical expert for commercial manufacturing of therapeutic proteins under cGMPs, with a 5PM–5AM rotating schedule (3-2-2).

You will oversee routine and complex manufacturing tasks, drive process improvements, lead investigations and CAPAs, and coach team members to ensure safety, quality, and schedule adherence.

Qualifications

• BS in science, engineering, biochemistry or related discipline.
• Minimum 5+ years of GMP-driven process operations in automated biotech manufacturing.
• Strong knowledge of GMP regulations and SOPs; experience in upstream and/or downstream unit operations.
• Proven ability to solve complex technical issues in biologics manufacturing.

Responsibilities

• Operate and oversee routine and complex manufacturing assignments.
• Coordinate change controls and drive process improvements.
• Act as acting Shift Supervisor/Manager in absence of the supervisor.
• Perform real-time process monitoring and data review.
• Lead investigations and CAPAs with cross-functional teams.

Skills

GMP knowledge

Process monitoring

Leadership

Problem solving

Coaching

Safety culture

Education

BS in science/engineering/biochemistry or related

Tools

DeltaV

Syncade

Pi Vision

SAP

Maximo

Infinity

Job description

Bristol Myers Squibb in the United States is seeking a Technical Lead to serve as the shift's technical expert for commercial manufacturing of therapeutic proteins under cGMPs, with a 5PM–5AM rotating schedule (3-2-2).

You will oversee routine and complex manufacturing tasks, drive process improvements, lead investigations and CAPAs, and coach team members to ensure safety, quality, and schedule adherence.