Senior Manager, ECQ Delivery
Bristol Myers Squibb · Summit West, NJ
The apply link worked recently (not employer-confirmed).
Role summary
This senior manager role oversees equipment commissioning and qualification activities at a multi-site pharmaceutical facility. Responsibilities include directing validation teams, managing project lifecycles, ensuring regulatory compliance, and maintaining qualified equipment systems. The position requires supervising multiple professionals and managing budgets across ongoing projects of moderate complexity.
What they're looking for
- Expert knowledge of cGMP, GXP, GAMP, SDLC regulations and 21 CFR Part 11
- Computer systems validation and good documentation practices experience
- Equipment commissioning and qualification program management expertise
- Supervisory experience managing multiple team levels and up to 50 personnel
- Project management across complex, multi-phase initiatives with budget oversight
- Strong technical and compliance guidance for validation activities
What you'll be doing
- Directly manage equipment commissioning and qualification teams performing validation activities
- Lead resource allocation and budget management for commissioning and qualification programs
- Oversee development and approval of procedures, protocols, and validation deliverables
- Supervise entry, junior, and experienced-level staff; conduct hiring and performance reviews
- Respond to customer support requests and maintain stakeholder communication on system status
Privacy & handoff
This role links to Bristol Myers Squibb's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.