Pharma Qualification Engineer: Quality & Compliance

Select Projects; Geel; Sur place; EUR 30 132 - 42 408; Plein temps

Avantages offerts par ce poste

Company car option

Meal vouchers

Eco-vouchers

Health insurance

End-of-year bonus

Holiday pay

Training via Select Academy

Résumé du poste

Select Projects is seeking a Qualification Engineer for an assignment with our client in Geel, Belgium. You will support the engineering team in qualifying equipment throughout its lifecycle, ensuring GMP/GDP and safety documentation are upheld.

You review and approve qualification and validation documents, assist with new or updated systems, and advise on cGMP aspects during qualification activities while maintaining clear communication with QA teams.

Qualifications

• You hold a professional bachelor’s or master’s degree in a scientific or technical field.
• You have proven work experience with qualification or validation activities in the pharmaceutical sector.
• You are knowledgeable about GMP, GDP, and safety documentation.
• Experience with change control management (TrackWise) is an asset.
• You have strong verbal and written communication skills.

Responsabilités

• Reviewing and approving qualification and validation documents (SOPs, URS, risk assessments, test plans, scripts, change controls, CAPAs, etc.).
• Supporting engineering teams with the introduction of new or updated systems and processes.
• Providing advice on cGMP aspects and compliance during qualification and validation activities.
• Following up on deviations and communicating status updates to QA teams.

Connaissances

verbal and written communication

Formation

Bachelor's or Master’s degree in scientific/technical field

Outils

TrackWise

Description du poste

Select Projects is seeking a Qualification Engineer for an assignment with our client in Geel, Belgium. You will support the engineering team in qualifying equipment throughout its lifecycle, ensuring GMP/GDP and safety documentation are upheld.

You review and approve qualification and validation documents, assist with new or updated systems, and advise on cGMP aspects during qualification activities while maintaining clear communication with QA teams.