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Planet Pharma Group

Project Manager, Sterility Assurance Systems & Process Engineering

Pay: $105–$125/hr

Posted: 2 days ago

Location: Bradley, IL (Onsite)

Last Updated: 4 hours ago

Hours: Full-Time

Expires: 10/4/2026

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What they do

An Engineering Manager oversees engineering and technical design of large projects, and manages communication and coordination among different types of engineers working on a project. Supervises project schedule, budget, and communications with stakeholders.

$154,424 / year median in Illinois

+4% projected growth

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Job Description

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