QA Validation

☞ Jefferson Wells

Visualizza: 175

Giorno di aggiornamento: 26-11-2025

Località: Wavre Walloon Brabant

Categoria: Produzione / Funzionamento

Industria:

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Contenuto del lavoro

  • Location: Wavre
  • Type: Contracting
  • Job #15283
QA Validation

Contracting – Walloon Brabant

#QA #validation #documentation #procedures #gmp #pharma

Are you a dynamic person? You have experience in validation in the pharmaceutical industry? Keep reading your future job description.

Our partner is looking for a QA Validation to join its team. This international company is well-known for its pharmaceuticals and vaccines.

What are your responsibilities?

As a QA Validation, you provide a compliance expertise in validation. To be successful in your role, here are your tasks:

  • Ensure QA oversight in validation activities (IQOQ / PQ / PV…)
  • Review/Approve the validation documentation regarding the GMP requirements and the procedures
  • Ensure that production practice are aligned with validation conclusion
  • Attend all project meetings as QA validation representative
  • Ensure timely escalation to Management of critical issues during validation
  • Contribute to the deviation process providing QA oversight and approving deviation for deviations related to validation activities and/or impact of manufacturing deviations to validation activities
  • Pro-actively identify potential quality and compliance risks and manage these risks through the risk register and quality plan process
  • To define the validation strategies through the change control process
  • To write and implement some validation documentation (Validation Plan, Validation Summary Report, Risk Assessment, Gap Analysis , Periodic review ….)
  • To ensure the correct application of the validation quality systems in the field and to define improvement plan as required
  • To support the production, QA and technical service teams in the implementation of the validation activities.

Who are you?

You have a university degree in a scientific domain. You have a relevant industrial experience in validation and quality assurance in a biopharmaceutical industry. You have a goog knowledge of GMP, CFR, Eudralex, … You have a good knowledge of different regulations and standards related to validation activities. You speak fluently French and English. You are solutions and achievment oriented. You are a good team player.

What can you expect?

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 Marie Defruit, [email protected]

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Scadenza: 10-01-2026

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