Remote QA CSV Specialist — GMP Validation Expert

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...

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...

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...

Do you thrive on ensuring every system meets rigorous validation standards while empowering a CMO's vision? Proclinical is seeking a QA CSV Specialist to support the validation and lifecycle management of computerized systems within a regulated environment. This role focuses on implementing industry best practices in alignment with GAMP regulations, driving...

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...

Do you thrive on ensuring every system meets rigorous validation standards while empowering a CMO's vision? Proclinical is seeking a QA CSV Specialist to support the validation and lifecycle management of computerized systems within a regulated environment. This role focuses on implementing industry best practices in alignment with GAMP regulations, driving...

A leading pharmaceutical consultancy in Switzerland is seeking a QA CSV Specialist to support validation and lifecycle management within a regulated environment. This role involves ensuring compliance with GMP regulations and collaborating with cross-functional teams. The ideal candidate holds a Bachelor's degree and possesses strong project management...

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...

A leading life sciences recruiter is seeking a QA CSV Specialist in Visp, Valais, Switzerland. This full-time position involves ensuring compliance with strict validation standards in a regulated environment. Candidates should possess a Bachelor's degree in a related field and strong understanding of system lifecycle and regulatory requirements. Excellent...