Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries?
Due to our constant growth, we are looking for a Medior Computer System Validation (CSV) Consultant to support our projects in Fleurus. This is a full-time position focused on the validation and documentation of regulated computerized systems within a GMP environment.
Collaborating with cross-functional teams including IT, Quality Assurance (QA), and Operations to ensure validation processes meet all regulatory requirements.
Ensuring the proper implementation of quality systems and maintaining high standards in all documentation processes.
Fluency in both French and English, with the ability to communicate effectively with cross-functional teams.
Ability to work independently and as part of a team.
Previous experience working in a pharmaceutical or medical device industry is preferred.
Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview.
As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills, and interact with colleagues from all corners of the world.