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Senior Project Manager; Pharmaceutical Manufacturing - CAPEX, GMP, CQV

Job in San Francisco, San Francisco County, California, 94199, USA
Listing for: GL Global
Full Time position
Listed on 2026-07-27
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist
  • Management
    Project & Program Management, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 150000 - 190000 USD Yearly USD 150000.00 190000.00 YEAR
Job Description & How to Apply Below
Position: Senior Project Manager (Pharmaceutical Manufacturing) - CAPEX, GMP, CQV

Senior Project Manager (Pharmaceutical Manufacturing) - CAPEX, GMP, CQV

Are you an experienced Project Manager with a proven track record of delivering capital projects within pharmaceutical manufacturing?

We are looking for a Senior Project Manager to lead the delivery of major CAPEX projects across pharmaceutical manufacturing facilities. You'll be responsible for managing projects from business case and design through construction, commissioning, qualification (CQV), and handover, ensuring safe, compliant, and on-time delivery.

What you'll bring:

  • Proven experience delivering CAPEX projects within pharmaceutical manufacturing or another highly regulated industry.
  • Strong knowledge of GMP environments, CQV, validation, and FDA/EMA compliance.
  • Experience managing multidisciplinary teams, contractors, and engineering partners throughout the full project lifecycle.
  • Ability to manage project scope, budgets, schedules, risks, and stakeholder engagement to ensure successful delivery.
  • Strong communication skills with the ability to work effectively across engineering, quality, operations, procurement, and senior stakeholders.
  • Degree qualified in Engineering, Project Management, or a related discipline. Project management certification (APM, PMP, PRINCE2) is advantageous.

This is an excellent opportunity to deliver high-value investment projects that improve manufacturing capability, compliance, and operational performance within a leading pharmaceutical environment.

If you're looking to lead technically challenging projects in a GMP-regulated manufacturing environment, we'd love to hear from you.

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Position Requirements
10+ Years work experience
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