PM parenterals

Join a leading global life sciences organisation at the forefront of pharmaceutical product development. This is your chance to take ownership of critical parenteral equipment projects in a multi‑product pilot plant environment, where sterile manufacturing excellence meets cutting‑edge engineering.

As a C&Q Project Manager you will…

• Lead planning, execution, and documentation of equipment qualification/validation for parenteral manufacturing systems (e.g. processors, fill‑finish, CIP/SIP, lyophilizers, autoclaves, dry heat ovens, nano‑milling).
• Prepare, execute, and review aseptic process simulations, including media fills and re‑validations.
• Draft technical specifications, URS, risk assessments, and validation protocols/reports.
• Manage FAT/SAT, commissioning, and construction supervision for new or modified equipment.
• Facilitate GMP risk analyses and lead CAPA/change control management.
• Act as equipment owner in multidisciplinary teams, liaising with QA and other stakeholders.
• Drive improvement initiatives and gap assessments within the pilot plant environment.

As a C&Q Project Manager you have…

• Master's degree in a technical field (or equivalent experience).
• 5+ years' pharmaceutical engineering experience with proven qualification/validation expertise.
• Strong GMP, GDP, and data integrity knowledge.
• Direct experience with parenteral manufacturing equipment & aseptic processing.
• Expertise in risk analysis tools (FMEA) and regulatory compliance.
• Project leadership skills using FPX or equivalent methodologies.
• Professional fluency in Dutch and strong English communication skills.
• Proficiency in MS Office (Excel, Word, Teams, MS Project).
• Willingness to travel ~20% for FAT activities.