QA Operations Specialist

eBR (Electronic batch record) Reviewer QA / OPsat KPC International4 days agoElectronic Batch Reviewer 3–6-month contract Immediate start.Visp, Valais, Switzerland (On-site)KPC International - Excellence from Concept to CompletionKPC International began operations in 2001, our team of Engineers and Scientists have helped our clients achieve project success...

A leading life sciences company in Visp, Switzerland, is looking for a QA specialist to join its operations team. This role involves coordinating QA interests, managing quality-related records, and supporting project-specific QA tasks in a cGMP environment. Ideal candidates will have a bachelor's or master's degree in biotechnology or biochemistry,...

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...

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...

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...

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...

In this role, the QA Specialist in Qualification will ensure quality assurance for new pharmaceutical facilities. The specialist will collaborate with project teams to ensure compliance with regulatory standards, guiding qualification strategies. Key responsibilities include representing QA in qualifications, coordinating QA interests, compiling...

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...

Senior QA Specialist (f/m/d) 80‑100% Location: Visp, Switzerland. Lonza is a global leader in life sciences operating across five continents. We’re looking for a QA specialist to join the multifunctional QA Operations team in the Bioconjugates Business unit and support the establishment and maintenance of quality management & compliance processes. You...

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...