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;
