Project Manager CQV – Life Sciences (Flanders)

 We are currently looking for a Project Manager CQV to start on a project at one of our clients within the pharmaceutical industry in Flanders.

Main responsibilities

• Define and align project scope, planning, and budget.
• Organize the project team.
• Draft technical specifications and lead the tendering process.
• Prepare and execute FAT, SAT, and commissioning activities.
• Supervise construction works.
• Create lifecycle documents such as URS, Risk Assessments, IOPQ.
• Execute and document protocols and summary reports.
• Perform and document tests in compliance with GMP guidelines, CFR21 Part 11, and testing procedures.
• Knowledge of data integrity, user access, and security settings.
• Participate in safety analyses such as SWIFT, HAZOP, FMEA, etc.
• Document quality incidents, deviations, and follow-up actions as per the protocol.

Main requirements

• Master’s degree in Industrial Sciences or equivalent through experience.
• Broad technical knowledge; experience with OSD equipment is a plus.
• 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).
• Quick understanding of P&IDs and other technical documents with the ability to translate them into a solids system.
• Experience: ≥ 7 years (for a medior 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.

What ALTEN has to offer

• A permanent contract
• A salary package in line with your experience and extra benefits (meal vouchers, recovery days, insurances)
• The possibility to join a great team and be part of the success story of an international group