QA Validation

☞ AUSY by Randstad

Ver: 170

Día de actualización: 16-11-2025

Ubicación: Wavre Walloon Brabant

Categoría: Gerencia ejecutiva Producción / Operación Mecánica / Técnica Mantenimiento

Industria:

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Contenido de trabajo

You have a previous experience as QA validation in a biopharmaceutical company? this position is for you !
Feel free to contact me : julie.licoppe@professionals.randstad.be


The QA Validation Consultant must be able to:

  • Understand quickly the characteristics and the mechanism of a broad range of production equipment and process including their potential impact on product and patient safety
  • Use a risk based approach for problem solving and prioritization of tasks
  • Blow aquality and compliance mindset through the validation activities
  • Develop and continuous improve expertises linked to the primary validation activities

The function requires:

  • A knowledge of good practices in biopharmaceuticals
  • A knowledge of different regulations and standards related to validation activities
  • to maintain andkeep up to date its knowledge and experience necessary to the function


We offer an attractive salary with extra-legal advantages :

  • Group insurance
  • Hospitalisation insurance
  • Meal vouchers of 7 euros gross per working day
  • Reimbursement km or company car
  • Monthly allowance (80 euros net per month)
  • A 13th month
  • Training
  • Etc.
A rate as freelance is also possible.


Our client – one of the world’s leading research-based pharmaceutical and healthcare companies – is committed to improving the quality of human life by enabling people to do more, feel better and live longer.


The QA Primary Validation Consultant ensures the QA oversight of the continuous validation activities for one or several vaccine bulk production units.

Mains objectives of this function are:

  • To take part in the establishment, the implementation, the follow-up and the maintenance of the continuous validation plan (CVP),
  • To define the validation strategies through the change control process (RPC),
  • To writ some validation documentation (VP, VSR, Risk Assessment, Gap Analysis)
  • To review and approve specific qualification and validation documentation (IQ, OQ, PQ, PV),
  • To ensure the correct application of the validation quality systems on the field and to define improvement plan as required
  • To support the production & technical services teams in the implementation of the validation activities
  • To ensure the adequate management of validation deviation (be QA GMP Responsible) and potentials CAPA (be Compliance Authority).
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Plazo: 31-12-2025

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