A leading recruitment partner in Life Sciences is seeking a QA CSV Specialist for a one-year contract in the Valais area, Switzerland. The role requires extensive experience in CSV within the Pharma industry, focusing on implementing best practices in compliance with GAMP regulations. Responsibilities include acting as a liaison for QA CSV, monitoring industry trends, and developing project plans. Candidates must have a relevant degree, Swiss residency or EU citizenship, and English proficiency. Hybrid work is possible with 2 days of home office. #J-18808-Ljbffr