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Project Manager, Facility Engineering & Cleanroom Infrastructure

Job in Bradley, Kankakee County, Illinois, 60915, USA
Listing for: Planet Pharma
Full Time position
Listed on 2026-09-05
Job specializations:
  • Engineering
    Quality Engineering, Regulatory Compliance Specialist, Validation Engineer
Salary/Wage Range or Industry Benchmark: 95 - 115 USD Hourly USD 95.00 115.00 HOUR
Job Description & How to Apply Below

Project Manager, Facility Engineering & Cleanroom Infrastructure

Location: Bradley, IL (100% Onsite)
Duration: October 2026 - December 2028
Employment Type: Contract Consultant

Pay Rate: $95-$115/hour + expenses

Position Overview

We are seeking a Project Manager to lead facility and infrastructure improvement projects within a highly regulated pharmaceutical manufacturing environment. The successful candidate will manage projects involving clean rooms, HVAC systems, material flows, personnel flows, environmental controls, facility modifications, and GMP compliance initiatives.

Key Responsibilities
  • Lead facility engineering and infrastructure projects.
  • Manage 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.
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 clean rooms and controlled environments.
  • Experience managing facility modifications or capital projects.
  • Strong knowledge of GMP manufacturing environments.
Preferred Qualifications
  • HVAC design or upgrade experience.
  • Facility remediation experience.
  • Material and personnel flow optimization experience.
  • Aseptic manufacturing experience.
  • Cleanroom classification knowledge.
  • Engineering consulting or owner's representative experience.
  • Commissioning and qualification support experience.
Target Experience
  • Pharmaceutical manufacturing facilities
  • Vaccines
  • Biologics
  • Sterile injectables
  • Medical device manufacturing
  • Regulated production environments
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