Validation – Senior

  • Lieu: Wavre
  • Travail #24060

Validation – Senior

Contracting – Brabant Wallon
 

Your responsibilities ?  

The mission consists of:

  • Ensuring quality for the validation part in the relevant projects (e.g., PUPSIT, RTU, …)
  • Conducting QA Oversight of validation activities
  • Actively participating in defining validation strategies in collaboration with project/validation teams and in compliance with GS requirements
  • Reviewing and approving all documentation related to validation (URSFMEA-LRA-CRA-DQ-IOQ-PQ-Leveraging Reports)
  • Participating in deviation investigations and troubleshooting

Key responsibilities:

  • Reviewing and approving all documentation related to the projects under their responsibility: validation plans, validation summary reports, URS, FMEA, Leveraging Reports, IQOQ protocols and reports, PQ protocols and reports, CRA, LRA
  • Actively participating in the project and process design phase to understand the project and establish an appropriate implementation and validation strategy
  • Establishing workload planning based on project schedules
  • Ensuring the chronological and logical execution of validation activities
  • Actively participating in project follow-up meetings, troubleshooting, and addressing various issues to anticipate validation impacts or risks and contribute to developing solutions
  • Ensuring QA Oversight of implemented methods
  • Providing coaching/transferring/handover of knowledge related to different projects

Your profile ?

  • Engineer or university degree in biotechnology, agronomy, chemistry, pharmacy, etc.
  • Minimum of 5 years of experience in an aseptic laboratory/industry, quality, or production environment
  • Experience in a regulated environment such as cGMP
  • Experience in industry validation; and in specific documents: URS, FMEA, Leveraging Reports, LRA (L=Leachables), CRA (C=Compatibility)
  • Knowledge of IPV (In-Process Verification) and PA (Proces Analytical Technology) processes is a plus
  • Advanced knowledge of aseptic technologies, closed systems
  • Experience as a QA Validation professional
  • Knowledge of GMP and aseptic environments

Our offer ?

We offer you a permanent contract and an attractive salary package. You'll also benefit from the opportunity to develop personally and professionally through in-house training.
If you're interested, don't wait any longer!

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