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Project Manager, Sterility Assurance Systems & Process Engineering

Job in Bradley, Kankakee County, Illinois, 60915, USA
Listing for: Planet Pharma
Full Time position
Listed on 2026-09-05
Job specializations:
  • Engineering
    Regulatory Compliance Specialist, Validation Engineer
Salary/Wage Range or Industry Benchmark: 105 - 125 USD Hourly USD 105.00 125.00 HOUR
Job Description & How to Apply Below

Project Manager, Sterility Assurance Systems & Process Engineering

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

Consultant Compensation

Pay Rate: $105-$125/hour

Position Overview

We are seeking a Project Manager with expertise in sterile manufacturing systems and process engineering to oversee implementation of critical compliance, process improvement, and equipment qualification initiatives. This individual will manage projects involving aseptic processing technologies, sterile filtration systems, manufacturing equipment upgrades, commissioning, validation, and operational readiness activities.

Key Responsibilities
  • Lead process-focused engineering projects from initiation through completion.
  • Manage equipment implementation and qualification activities.
  • Coordinate cross-functional engineering and operational teams.
  • Support vendor selection, procurement, and technical reviews.
  • Develop project plans, schedules, budgets, and risk mitigation strategies.
  • Ensure project deliverables meet quality and compliance requirements.
  • Support commissioning, qualification, and validation execution.
  • Facilitate stakeholder communication and project governance.
  • Drive resolution of technical and operational challenges.
  • Maintain accurate project documentation and reporting.
Required Qualifications
  • Bachelor’s degree in Engineering, Life Sciences, or related discipline.
  • 10+ years of pharmaceutical or biotechnology experience.
  • Significant experience in sterile manufacturing environments.
  • Project management experience supporting technical and engineering initiatives.
  • Experience with qualification and validation programs.
  • Strong knowledge of GMP requirements.
Preferred Qualifications
  • Sterile filtration experience.
  • Container closure integrity testing (CCIT) experience.
  • Fill-finish manufacturing experience.
  • Isolator technology experience.
  • Sterility assurance experience.
  • Aseptic processing expertise.
  • Risk assessment and quality systems experience.
Target Backgrounds
  • Process Engineering Manager
  • Manufacturing Engineering Manager
  • Validation Project Manager
  • Technical Project Manager
  • Sterility Assurance Manager
  • Pharmaceutical Engineering Manager
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