Head of Site Project Engineering

CSL•Kankakee, IL

10d

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.
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.
Collaborative team player with decision-making and influencing skills.

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.