Head of Site Project Engineering

CSL Plasma • Kankakee, IL

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About The Position

The Head of Project Engineering role is responsible for leading the end-to-end execution of strategic capital projects that expand manufacturing capacity and capability. This role ensures delivery of cGMP-compliant equipment and facilities that meet FDA and global regulatory standards, while aligning with enterprise-wide strategic objectives. The incumbent will lead cross- functional teams through the full project lifecycle—from scoping and design through procurement, construction, qualification, and turnover to commercial operations.

Requirements

• Bachelor’s degree in engineering (Chemical, Mechanical, Electrical) required, a master’s preferred.
• Minimum of ten years’ experience in the pharmaceutical, food, or chemical process industry.
• 5+ years’ experience in engineering and/or leadership roles in project management/engineering, in the chemical industry
• Experience in process control, automation, construction, quality, project management, safety, and engineering.
• Collaborative team player with decision-making and influencing skills.
• Strong understanding of cGMPs and FDA regulations.
• Knowledgeable in project management principles, risk management, and critical path analysis.
• Financial acumen in managing multimillion-dollar budgets.
• Ability to lead cross-functional teams and manage multiple projects.
• Strategic thinker with a proactive approach to problem-solving.

Nice To Haves

• PMP certification preferred.
• Experience with biologics, sterile manufacturing, and advanced modalities (e.g., ADCs, mRNA).
• Familiar with validation, CMC, and regulatory submission requirements.

Responsibilities

• Project Leadership & Execution: § Lead multi-disciplinary teams through all phases of project delivery, ensuring alignment with global and local strategic goals. § Oversee the development, procurement, construction, and qualification of new equipment and facilities to meet production throughput demands. § Ensure projects are executed in alignment with CSL’s Operating System (COS), Site Management System (SMS), and global engineering standards. § Ensure projects are delivered on time, within budget, and in compliance with cGMP and regulatory requirements.
• Strategic Alignment & Governance: § Ensure all initiatives are aligned with business objectives and the strategic philosophy of the organization. § Translate CSL’s long-term capacity and technology strategies into executable site-level project plans. § Provide regular updates to senior site leadership and global steering committees, including financial status, schedules, risks, and progress summaries.
• Compliance & Quality § Ensure all project activities result in facilities and processes suitable for FDA and global regulatory approval. § Partner with Quality Assurance and Regulatory Affairs to support validation and submission requirements.
• Resource Management § Manage internal and external resources, including engineering firms, contractors, and consultants. § Build and maintain high-performing project teams with clear accountability and performance metrics.
• Completes any other duties/responsibilities assigned by senior management.

Benefits

• For more information on CSL benefits visit How CSL Supports Your Well-being | CSL
• At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1,001-5,000 employees