Job DescriptionMy client, an Innovative Global Medical Device Company is looking to on-board a Validation Engineer to join their growing Quality team on a contractual basis (6 months). The individual hired will follow the validation procedure outlined, working on each of the different phases aligned to operational objectives, statutory and regulatory requirements and the principles of GMP. The role incorporates the delivery and documentation of validation procedures & reporting.
They are looking for an engineer with experience in a regulated environment that has worked on Medical Device projects with knowledge of FDA and European regulations.
You will be based in Nyon, Switzerland and have a full time contract - 40 hours per week. You will receive a great base rate and additional benefits.
- 3 years Validation experience
- Fluent in French & English
- Degree in Engineering or Science