Location: On-site
Contract: Until 31 December 2026
Function: Engineering
About the Role
We are seeking an experienced Project Manager - Engineering & Automation to lead automation and process equipment projects within a highly regulated CAR-T manufacturing environment.
This position sits within the Engineering & Automation department and works closely with the Director and Managers of the Make Asset Management (MAM) function. The role combines technical depth in GxP-compliant automation systems with strong project leadership and stakeholder management capability.
This is a hands-on engineering project management role in a pharmaceutical/biotech setting - not a purely administrative PM position.
Key Responsibilities
Project & Portfolio Leadership
- Manage long-term planning of engineering and automation projects.
- Initiate and deliver projects aligned to departmental strategy and capacity planning.
- Own full project lifecycle (scope, budget, timeline, risk, and reporting).
- Support portfolio-level resource planning and prioritization.
- Represent engineering projects to internal MAM stakeholders and external partners.
Automation & Technical Scope
- Lead design and implementation of GxP-compliant automation systems.
- Oversee historian integration and server-hosted software for equipment connectivity.
- Manage PLC and HMI system design and deployment.
- Ensure compliance with GMP and data integrity standards.
- Resolve complex technical challenges impacting operational priorities.
Compliance & Continuous Improvement
- Ensure systems meet regulatory and validation requirements.
- Identify and implement continuous improvement initiatives.
- Support knowledge management, capability development, and training of junior engineers.
- Conduct gap analyses to strengthen departmental performance.
Requirements
- Master’s degree in Engineering or equivalent through experience.
- 10+ years of relevant professional experience.
- Minimum 5 years in project management or people leadership roles.
- Proven experience in automation engineering within GMP/GxP-regulated environments.
- Strong knowledge of PLC, HMI, and historian systems.
- Demonstrated stakeholder management experience in a manufacturing environment.
Preferred Experience
- Pharmaceutical or biotech manufacturing background.
- Systems engineering expertise.
- Experience with qualification and validation of pharmaceutical systems.
- Exposure to advanced therapy or cell therapy manufacturing environments.
What We’re Looking For
- Strong safety and quality mindset.
- Clear and effective communicator, able to explain complex engineering concepts.
- Structured and solutions-oriented approach.
- Transparent and accountable in project execution.
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