From the 19 March 2020
Academic degree(s) with focus on qualification / validation.
First experience in qualification / validation in the pharmaceutical, biotech, chemical or similar industries.
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.