CQV engineer

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;