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Pharmaceutical industry





  • Start date

    From the 19 March 2020

Ideal profile

  • Educational background

    Academic degree(s) with focus on qualification / validation.

  • Experience

    First experience in qualification / validation in the pharmaceutical, biotech, chemical or similar industries.

Proposed project

Reporting to the Head of Qualification / Validation, you are in charge of the commissioning and qualification of production and laboratory equipment.

In this role you write protocols and perform acceptance tests at the supplier and at the customer site (FAT/SAT).

You are also responsible for the Installation, Operational and Performance Qualification (IQ, OQ, PQ) and write the reports.

Finally, in collaboration with the Validation Department, you work on various process validation projects (e.g. cleaning, sterility, freeze-drying).

On the other hand, you are responsible for the drafting of Validation Plans (VMP) up to Validation reports.

The different steps to integrate the tribe

  • First interview with the HR team
  • Technical interview with a Business Engineer
  • Physical meeting in our office and constitution of the skills file
  • Last exchange with one of our leaders

Apply for this position

Join the tribe !