A pharmaceutical organisation is seeking an experienced Commissioning, Qualification & Validation (CQV) Engineer to manage validation activities related to equipment and facilities in a cGMP-regulated environment. The candidate will prepare technical documentation, execute validation protocols, and ensure compliance with cGMP requirements. The role requires a Bachelor's degree and significant industry experience. Strong communication and organisational skills are essential. This position is 100% on-site in Switzerland, Wallis. #J-18808-Ljbffr