• Are you a structured, conscientious, and precise fast learner?
• Are you a real team player who can also work independently?
• Do you have a CAN-DO mentality who can think proactively?
• Do you have the knowledge and practical experience of the latest developments in the CSV (Computer system validation) and cGMP.

We love meeting smart and forward-thinking talents, so don’t hold back!

• You will be part of a young team of CSV engineers under the guidance of a project manager.
• You will prepare project CSV deliverables:
  • User Requirement Specifications
  • Risk and Impact Analysis/Assessment (Process, Business, EHS, Regulatory)
  • Validation Master Plan (VMP)
  • Design Review/Qualification
  • Test Matrices
  • FAT, SAT, Commissioning, IQ, OQ, PQ protocols and reports
• You will broaden your knowledge of current industry standards, regulatory requirements, and Authority expectations regarding CSV.
• You will support the project schedule for CSV activities.
• You will organize, execute and document CSV testing.
• You will support during system/installation start-up in the function of CSV test activities.
• You will set up and follow up of Project documentation System and Management.
• You will work in close collaboration with Project, Engineering, and CQV Management.

The projects are mainly situated in the Life science/Biotech Industry:

• Vaccines: m-RNA, viral vector, mAbs…
• Cell/gene/protein therapies
• DS/DP/Formulation/Filling

The projects consist of the following packages/discipline:

• Facilities: HVAC, cleanroom finishes, Interlock, EMS,
• Clean Utilities production, storage and distribution (WFI, PW, PS, clean gasses)
• Prim. & Sec. Process equipment: bioreactors, filter systems, autoclaves , decontamination systems, ….
• Filling systems
• Automation and process control

We are looking for different people in different regions:

• Wallonia
• East/West Flanders and Antwerp
• Limburg, Kempen and adjacent Netherlands

The CSV Engineer has proven record of

• a (Professional) Bachelor or a Master’s degree (or equivalent by experience), ideally in automation-regulation, IT or relevant other expertise.
• a first experience in Life Sciences industries and industrial automation processes.

The CSV Engineer has

• excellent communication skills in English, French and/or Dutch (written and spoken).
• knowledge of current Industry Standards, Regulatory requirements and Authority expectations (Eudralex, FDA, PICS, ICH, ISO, ASTME2500, ….) is an advantage.
• a field experience with the following is an advantage:
• Scada, supervision and computerized system
• IT regulation
• Computerized System Validation

Besides an exciting flexible environment, a unique chance to participate in challenging and innovative projects and interaction with inspiring colleagues, who have a professional attitude and attach considerable importance to teamwork.

We stand for:

• a challenging position
• a full time contract
• location: Flexible depending to clients’ locations
• a challenging job in a dynamic and knowledge-sharing network company
• the freedom to develop yourself in line with your ambition
• a great autonomy in your role, an excellent working atmosphere within a great team of Experts in their domain
• a competitive salary
• other benefits including a company car, fuel card, lunch vouchers, eco vouchers, pension plan, phone subscription