QA CSV Specialist
vor 2 Wochen
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 GAMP regulations. - Strategic implementation of CSV process improvements and tactical support of CSV operations to meet the changing needs of the business. - Continually monitor industry regulation and trends and apply this knowledge to optimize clients policies and procedures. - Carry-out a variety of tasks relating to the validation and lifecycle management of computerized systems including process control systems (MES, Delta V), spreadsheets and bench top equipment. - Provide expert technical guidance for GMP decisions regarding the validation and lifecycle management of computerized systems - Responsible for implementing continuous improvements, procedures and, local Validation Plans and Master Plans - Ensure the department is operating as efficiently as possible by eliminating activities that do not positively impact production capacity or compliance. - Develop a project scope, implementation plan and tracking mechanisms, while being forward looking to identify roadblocks and solutions prior to issues affecting the project schedule. - Actively audit projects and systems to ensure that the appropriate validation activities are carried out and are in compliance with regulatory requirements & corporate standards - In conjunction with engineering, automation, operations and other departments, evaluate new applications in order to identify validation requirements - Act on behalf of, or be a conduit to, the QA CSV Manager on CSV issues to ensure that GMP issues are identified and addressed timely and correctly. Qualifications: - Education Required: Bachelors degree in Engineering, Information Technologies, Natural Sciences or related - Advanced Level Pharma Industry minimum 5 years experience. - Experience and in-depth understanding of all system lifecycle deliverables from Commissioning & Qualification (C&Q) and Computer System Validation (CSV) documentation - Knowledge of applicable regulatory requirements (GMP Annex 11, 21CFR, GAMP, PICS...). - Language: English required, German advantage Christopher Woodward
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QA CSV Specialist
vor 1 Woche
Visp, Schweiz Gi Group VollzeitQA 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...
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QA CSV Specialist
vor 2 Wochen
Visp, Valais, Schweiz Gi Group Vollzeit CHF 90'000 - CHF 120'000 pro JahrQA 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...
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QA CSV Specialist – 6760 ASH
vor 1 Tag
Visp, Schweiz CTC Resourcing Solutions VollzeitCTC 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...
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QA CSV Specialist
vor 2 Wochen
Visp, Schweiz Actalent VollzeitJoin 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...
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QA CSV Specialist
vor 3 Wochen
Visp, Schweiz Proclinical Group VollzeitDo 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...
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QA CSV Specialist
vor 1 Woche
Visp, Schweiz Proclinical Staffing VollzeitDo 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...
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Hybrid QA CSV Specialist – Pharma
vor 1 Tag
Visp, Schweiz CTC Resourcing Solutions VollzeitA 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...
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Hybrid QA CSV Specialist — Pharma/GAMP
vor 1 Woche
Visp, Schweiz Gi Group VollzeitA 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...
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QA CSV Consultant
Vor 2 Tagen
Visp, Valais, Schweiz Consultys Suisse Vollzeit CHF 80'000 - CHF 120'000 pro JahrWe 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...
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QA CSV Specialist — Regulated Systems
vor 3 Wochen
Visp, Schweiz Proclinical Group VollzeitA 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...
