Hybrid CSV Compliance Lead

A recruitment agency is seeking a QA CSV Specialist in Switzerland. This contract role involves ensuring compliance with regulation and managing CSV processes effectively within the pharmaceutical sector. The ideal candidate will have a Bachelor's degree and extensive experience in the industry, coupled with strong project management and communication...

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...

QA CSV Specialist (m/f/d) 📄 Contract: Temporary - 1 year Summary: The QA CSV Specialist plays a key role in defining and implementing industry best practices for Computer System Validation (CSV) within the framework of GAMP regulations. This position combines strategic initiatives to improve CSV processes with hands‑on support for operational...

Join the team as a QA CSV Specialist and play a key role in ensuring compliance and driving continuous improvement in computerized system validation (CSV) processes. Duration: 1 year Home Office: 2 days Your Responsibilities Represent QA and act as liaison for CSV-related topics. Implement and optimize validation processes in line with GAMP, GMP Annex 11, 21...

CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed. Our client, a global market leader in the...

CSV Subject Matter Expert (SME) – Leadership Role in Pharma/BiotechAre you ready to take ownership of Computer System Validation (CSV) across critical systems in a fast-paced, innovative environment? We're seeking aCSV SMEto lead validation activities for platforms such as eQMS, LIMS, and ERP, ensuring compliance with GAMP 5 and data integrity...

QA CSV Specialist (m/f/d) Start: Jan 2026 Location: Visp, Valais Contract: Temporary - 1 yearSummary:The QA CSV Specialist plays a key role in defining and implementing industry best practices for Computer System Validation (CSV) within the framework of GAMP regulations. This position combines strategic initiatives to improve CSV processes with hands-on...

Jobdescription QA CSV Specialist For our Client in Visp we are searching for a Computer System Validation Specialist/Engineer (CSV) to carry out a variety of tasks related to the validation and lifecycle management of computerized systems Key Responsibilities: - Identify or create industry best practices and implement these within the framework of existing...

We are looking for a QA CSV Specialist to join our teams in Visp and support the Quality Assurance department in ensuring robust validation and lifecycle management of computerized systems.Your ResponsibilitiesServe as the primary QA CSV representative, acting as a liaison between QA and internal/external stakeholders to ensure clear alignment on CSV...

Main responsibilities: Identify or create industry best practices and implement these within the framework of existing GAMP regulations Implementing continuous improvements, procedures and local Validation Plans and Master Plans to ensure the department is operating as efficiently as possible by eliminating activities that do not positively impact production...