Lead, Equipment Qualification & Commissioning

Biopharma Careers; Summit West (CA); On-site; USD 125,000 - 152,000; Full time

Benefits offered by this job

Health Coverage

401(k) plan

Paid Time Off

Stock options may be available

Employee assistance programs

Job summary

Bristol Myers Squibb is seeking a Senior Manager, Equipment Commissioning & Qualification Delivery to oversee multi-site equipment qualification and validation programs. You will lead large teams, coordinate with internal customers and external providers, and ensure on-time, on-budget delivery of critical GMP activities.

The role emphasizes budgeting, regulatory compliance, and cross-functional leadership across site operations, engineering, and QA teams in a fast-paced pharmaceutical setting.

Qualifications

• BS in Engineering or Science required with minimum 7 years in pharmaceutical validation.
• Experience leading large teams and projects in GMP environments.
• Strong knowledge of cGMP, 21 CFR Part 11 and computer systems validation.

Responsibilities

• Directly manage ECQ equipment qualification and computerized system validation teams.
• Lead projects with up to 50 staff across multiple departments.
• Maintain budgets, resource forecasting and safety/compliance adherence.

Skills

ECQ Leadership

Regulatory Compliance

Budget Management

Cross-functional Collaboration

Project Management

cGMP / GXP

Education

BS in Engineering or Science

Tools

CMMS

Microsoft Office

Validation Software

Job description

Bristol Myers Squibb is seeking a Senior Manager, Equipment Commissioning & Qualification Delivery to oversee multi-site equipment qualification and validation programs. You will lead large teams, coordinate with internal customers and external providers, and ensure on-time, on-budget delivery of critical GMP activities.

The role emphasizes budgeting, regulatory compliance, and cross-functional leadership across site operations, engineering, and QA teams in a fast-paced pharmaceutical setting.