Senior Project Manager, GMP Cleanroom & Facility Engineering

Planet Pharma

Bradley (IL)

On-site

USD 272,214,000 - 328,420,000

Part time

6 days ago
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Job summary

Planet Pharma is seeking an experienced Project Manager to lead facility engineering and infrastructure improvements within a highly regulated pharmaceutical environment.

The role focuses on cleanrooms, HVAC systems, material and personnel flows, and GMP compliance initiatives, with 100% onsite work in Bradley, IL. Excellent coordination with Quality, Validation, Manufacturing, and Facilities teams is required.

Qualifications

  • Bachelor's degree in Engineering or related discipline.
  • 10+ years of pharmaceutical, biotech, or life sciences experience.
  • 7+ years of project management experience.
  • Experience with cleanrooms and controlled environments.
  • Experience managing facility modifications or capital projects.
  • Strong knowledge of GMP manufacturing environments.

Responsibilities

  • Lead facility engineering and infrastructure projects.
  • Coordinate engineering design reviews and contractor activities.
  • Coordinate cleanroom and HVAC improvement initiatives.
  • Support construction planning, execution, and turnover.
  • Drive schedule development and project tracking.
  • Manage project budgets, risks, and change controls.
  • Support commissioning and qualification activities.
  • Coordinate with Quality, Validation, Manufacturing, and Facilities teams.
  • Ensure projects meet GMP and regulatory requirements.
  • Provide routine status updates and reporting.

Skills

Project management
GMP compliance
Facility management
HVAC systems
Regulated environment
Stakeholder coordination

Education

Bachelor's degree in Engineering or related discipline

Job description

Planet Pharma is seeking an experienced Project Manager to lead facility engineering and infrastructure improvements within a highly regulated pharmaceutical environment.

The role focuses on cleanrooms, HVAC systems, material and personnel flows, and GMP compliance initiatives, with 100% onsite work in Bradley, IL. Excellent coordination with Quality, Validation, Manufacturing, and Facilities teams is required.

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