QC Equipment Lifecycle Lead, Cell Therapy

Bristol Myers Squibb; Massachusetts; On-site; USD 91,000 - 110,000; Full time

Job summary

Bristol Myers Squibb in Devens, MA, seeks a Senior Specialist to manage the lifecycle activities of QC laboratory equipment and potentially serve as the QC equipment system owner. This role requires navigating GMP/cGMP requirements and collaborating with cross-functional teams.

You will create user requirements and validation protocols, coordinate commissioning and decommissioning, perform qualifications and calibrations, maintain records, and mentor others while driving continuous improvement.

Qualifications

• Experience with equipment qualification and validation.
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Responsibilities

• Manage lifecycle activities of QC laboratory equipment and act as system owner.
• Create user requirements and validation protocols for equipment.
• Coordinate commissioning/decommissioning with QC and site engineering for labs.
• Schedule, perform qualifications, calibrations, maintenance and repairs.
• Maintain GMP-compliant records and logs.
• Train others on equipment lifecycle processes and drive continuous improvement.

Skills

Regulatory knowledge

Problem solving

Communication

Team collaboration

Time management

Technical writing

Education

Bachelor’s degree or equivalent

Advanced degree preferred

Tools

SAP

Valgenesis

Maximo

Job description

Bristol Myers Squibb in Devens, MA, seeks a Senior Specialist to manage the lifecycle activities of QC laboratory equipment and potentially serve as the QC equipment system owner. This role requires navigating GMP/cGMP requirements and collaborating with cross-functional teams.

You will create user requirements and validation protocols, coordinate commissioning and decommissioning, perform qualifications and calibrations, maintain records, and mentor others while driving continuous improvement.