ZipRecruiter

Log In

1

Senior Gmp Project Manager Jobs (NOW HIRING)

Anveta

Senior CSA CTOP Coordinator

Lebanon, IN

... GMP, project sequencing, and validation readiness requirements. The ideal candidate has hands-on ... Develop, manage, and track CSA CTOPs in alignment with project turnover strategy and schedule ...

Project Manager Construction

Be Seen First

Sr Project Manager

Naples, FL · On-site

$120K - $150K/yr

About the Role We are seeking a Senior Project Manager to join our team! In this role, you will oversee the management and delivery of complex construction projects, ensuring they are executed ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Ensure all projects are executed in compliance with GMP requirements, company procedures, and ... Experience managing multiple projects, stakeholders, and competing priorities simultaneously.

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Ensure all projects are executed in compliance with GMP requirements, company procedures, and ... Experience managing multiple projects, stakeholders, and competing priorities simultaneously.

Balfour Beatty

Senior Project Manager

Dallas, TX · On-site

Summary Balfour Beatty Construction is seeking a Senior Project Manager to join our Special ... Creates Project Incentive Compensation Plan within 30 days of GMP acceptance. Preconstruction ...

next page

Showing results 1-20

People also search for

All JobsSenior Gmp Project Manager Jobs

Senior Gmp Project Manager information

See salary details

$62.5K

$126.7K

$184.5K

How much do senior gmp project manager jobs pay per year?

As of Jun 7, 2026, the average yearly pay for senior gmp project manager in the United States is $126,702.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,500.00 and $146,000.00 per year, depending on experience, location, and employer.
Senior CSA CTOP Coordinator

Senior CSA CTOP Coordinator

Anveta

Lebanon, IN

Other

Posted 19 days ago

Job description

Senior CSA CTOP Coordinator

Location: Lebanon, IN 100% on site

Contract Length: 2+ Years

8+ years CTOP experience, some pharma required

Specific to CSA scope

Position Overview

The Senior CSA CTOP Coordinator is responsible for managing Construction Turnover Packages (CTOPs) for CSA scopes on large-scale pharmaceutical capital projects. This role serves as the link between construction, quality, commissioning, and project controls to ensure CSA systems are completed, documented, and turned over in compliance with GMP, project sequencing, and validation readiness requirements.

The ideal candidate has hands-on experience supporting CTOP execution on regulated life sciences projects and understands how CSA turnover directly impacts commissioning, qualification, and subsequent validation activities.

Key Responsibilities
  • Lead the CSA Construction Turnover Package (CTOP) process from mechanical completion through turnover to Commissioning/Quality
  • Develop, manage, and track CSA CTOPs in alignment with project turnover strategy and schedule milestones
  • Coordinate with CSA construction teams to verify system boundaries, punch list closure, and mechanical completion readiness
  • Work cross-functionally with Commissioning, CQV, QA, and Document Control to support timely and compliant system handover
  • Review and validate CSA turnover documentation, including:
    • As-built drawings
    • Inspection and test records
    • Material traceability and certifications
    • Punch list and deficiency closeout documentation
  • Maintain CTOP tracking logs and dashboards; provide regular status updates to project leadership
  • Participate in turnover meetings, walkdowns, and system readiness reviews
  • Ensure turnover packages meet GMP, FDA, and project-specific quality requirements
  • Identify risks to turnover readiness and proactively drive resolution with construction and project teams
  • Support audit readiness related to CSA construction and turnover documentation
Required Qualifications
  • 8+ years of experience in CSA construction, turnover, or project coordination roles within pharmaceutical, biotech, or regulated life sciences facilities
  • Direct experience managing or supporting CTOPs for CSA scopes on large capital projects
  • Strong understanding of:
    • CSA construction sequencing in GMP environments
    • Mechanical completion vs. system turnover requirements
    • How CSA readiness affects commissioning and qualification
  • Experience working onsite with EPC/EPCM teams and multiple subcontractors
  • Familiarity with GMP documentation standards and audit expectations
  • Proficiency with CTOP tracking tools, project management systems, and document control platforms
  • Excellent organizational, communication, and stakeholder coordination skills
Preferred Qualifications
  • Experience on large greenfield pharmaceutical manufacturing projects
  • Prior exposure to CQV interfaces for CSA systems (rooms, finishes, envelopes, etc.)

Apply