Overall, you are likely to take on the following responsibilities:
In dialogue with the client, you develop the validation strategy (VMP) as well as the validation plans in compliance with the quality standards;
You write the validation protocols;
You initiate, execute and supervise the validation operations of the packages entrusted to you;
You carry out documentary verification and approval during the project.
Profile:
Master or bachelor degree in the pharmaceutical field;
At least a first year of relevant experience in the pharmaceutical, medical devices or diagnostics industry;
GMP knowledge;
Teamplayer;
Very good communication, planning and organization skills;
You are fluent in French and have a good professional knowledge of English (being able to read and write technical documentation);
Offer:
An attractive salary package in line with your experience;
Through our Q-Academy we offer you an extensive training package to continuously increase your knowledge;
Work-life balance;