QA Specialist, CSV

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...

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...

:The "QA Specialist, CSV & Automation" is responsible for the qualification and validation compliance of equipment and computerized systems related to aseptic facilities, equipment and utilities related to the GMP manufacturing of drug products as part of Lonza CAPEX project portfolio in Stein, AG. Responsible for the compliance of commissioning and...

For our pharmaceutical client based in Visp, we are currently seeking an experienced QA Specialist, CSV & Automation to support large-scale CAPEX projects within a GMP-regulated manufacturing environment. Description The "QA Specialist, CSV & Automation" is responsible for the qualification and validation compliance of equipment and computerized systems...

TheQA CSV Specialistplays a key role in ensuring compliance and efficiency in the validation and lifecycle management of computerized systems. Reporting to the QA Validations & Qualifications Head, this position combines strategic process improvement with hands-on operational support, ensuring systems meet both regulatory requirements and business...

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...

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 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...