Validation Engineer
Contracting – Brabant Wallon
Your responsibilities ?
- Write final URS, finalize URS reviews
- Perform risk assessments, FMEA (quality and safety) and DoE
- Follow-up manufacturers (design, manufacturing, testing, FAT-SAT)
- Write and/or review validation protocols (FAT, SAT, IQ-OQ and PQ)
- Schedule and design validation activities, priorities, logistics, supplier interventions
- Perform or manage validation and flows of documentation
- Write standard Visual Inspection and/or Leak Detection instructions
- Write change management documents
Your profile?
- You have a scientific background or equivalent acquired through professional experience
- You have minimum 3 years experiences in validation and/or metrology
- You have an experience in Qualification/validation process in a pharmaceutical environment (GMP)
- You are a good communicator
- You are autonomous, rigorous, team player with a critical mind
Our offer?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply.
Do you have any questions? You can contact Anaïs Malikian, [email protected]
