From the 19 March 2020
Academic degree(s) with focus on quality assurance.
First experience in quality assurance in the pharmaceutical, biotech, chemical or similar industries.
As part of the Quality Department, you actively participate in the management and improvement of the quality system in compliance with GMP.
You launch and manage the deviation process • As part of your job, you are involved in the management of OOS quality deviations (out of specification) and OOT (out of trend).
After analyzing the causes, you’re able to implement corrective and preventive actions related to deviations (CAPA) as well as the processing of initiated change requests (Change Control).
In charge of writing quality procedures (SOP), you also participate in their reviews and approvals.
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