Equipment CQV Lead: GMP & Validation

Bristol Myers Squibb; Summit (NJ); On-site; USD 107,000 - 129,000; Full time

Benefits offered by this job

Flexible Time Off (FTO)

11 paid company holidays

Comprehensive benefits package

Annual company shutdown

Job summary

Bristol Myers Squibb is seeking a Project Engineer/Manager for Equipment Commissioning & Qualification (ECQ) Delivery in Summit, NJ. You will coordinate CQV activities for equipment, facilities, and utilities across a multi-product site, balancing project deadlines with budget constraints.

The role requires strong project leadership, familiarity with cGMP and validation practices, and the ability to manage a team while contributing hands-on as needed.

Qualifications

• BS in Engineering or a science-related discipline; substitution with relevant experience possible.
• Minimum of 7 years of experience in pharmaceutical validation/applications in GMP environments.
• Minimum of 3.5 years of experience managing personnel and/or projects.
• Strong instrumentation background for lab and manufacturing operations.
• Experience with investigations, deviations, and CAPA management.
• Ability to train, develop, delegate and motivate project teams.

Responsibilities

• Leads multiple projects or contractor teams to on-time, within-budget delivery.
• Coordinates project execution and resource allocation for CQV activities.
• Occasionally contributes to hands-on project work.
• Ensures compliance with cGMP, GXP, and 21 CFR Part 11 requirements.
• Maintains effective communication with stakeholders and customers.

Skills

Project management

cGMP knowledge

Interpersonal skills

Communication

Education

BS in Engineering or sciences

Tools

CMMS

Validation systems

GxP software

MS Office

Job description

Bristol Myers Squibb is seeking a Project Engineer/Manager for Equipment Commissioning & Qualification (ECQ) Delivery in Summit, NJ. You will coordinate CQV activities for equipment, facilities, and utilities across a multi-product site, balancing project deadlines with budget constraints.

The role requires strong project leadership, familiarity with cGMP and validation practices, and the ability to manage a team while contributing hands-on as needed.