CQV Project Manager Job Description
Main Tasks
* Define project scope, planning, and objectives.
* Lead a project team.
* Develop technical specifications and manage the tendering process.
* Prepare and execute FAT, SAT, and commissioning activities.
* Oversee construction works.
* Create lifecycle documents like URS, Risk Assessments, IOPQ.
* Document protocols and summary reports.
* Perform tests in compliance with GMP guidelines, CFR21 Part 11, and testing procedures.
* Ensure data integrity, user access, and security settings.
* Participate in safety analyses like SWIFT, HAZOP, FMEA, etc.
* Record quality incidents, deviations, and follow-up actions according to the protocol.
Requirements
* Masters degree in Industrial Sciences or equivalent through experience.
* Broad technical knowledge; experience with OSD equipment is advantageous.
* Project management experience – able to lead a project team.
* Preferably pharmaceutical experience with knowledge of machinery directives, ATEX regulations, PED regulations, piping standards, and risk analyses (HAZOP, FMEA).
* Rapid understanding of P&IDs and other technical documents with the ability to translate them into a solid system.
* Experience: ≥ 7 years (for a mid-level profile), preferably ≥ 12 years (for a senior profile).
* Fluency in written and spoken Dutch and English for daily professional use.
* Proficient in Microsoft Office (Excel, Word, etc.) and MS Project.
Job Offer
* A permanent contract.
* A salary package aligned with your experience and additional benefits (meal vouchers, recovery days, insurances).
* The opportunity to be part of an international group.
We look forward to getting to know you and your ambitions.