Quality Assurance CSV Specialist
vor 3 Wochen
Talent Acquisition Consultant at Coopers Group AG – Life Science Duration: 12 months Location: Visp Home office option: yes, 2 days home office possible For our Pharma client, we are looking for an experienced QA CSV Specialist, with minimum 5 years of experience in the Pharma industry. Main responsibilities Identify or create industry best practices and implement these within the framework of existing GAMP regulations. Implement continuous improvements, procedures and local Validation Plans and Master Plans to ensure the department operates efficiently by eliminating activities that do not positively impact production capacity or compliance. Develop a project scope, implementation plan and tracking mechanisms; 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 to identify validation requirements. Act on behalf of, or be a conduit to, the QA CSV Manager on CSV issues to ensure GMP issues are identified and addressed timely and correctly. Your experience Bachelor’s degree in Engineering, Information Technologies, Natural Sciences or related. Fluent in English required; German is an advantage. Minimum 5 years experience in the Pharma industry. Experience and in-depth understanding of all system lifecycle deliverables from Commissioning & Qualification (C&Q) and Computer System Validation (CSV) documents through System Retirement, as well as the regulatory requirements applicable (GMP Annex 11, 21CFR, GAMP, PICS...). Seniority level Mid-Senior level Employment type Contract Job function Quality Assurance Industries: Pharmaceutical Manufacturing Get notified about new Quality Assurance Specialist jobs in Visp, Valais, Switzerland. #J-18808-Ljbffr
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QA CSV Specialist
vor 3 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 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 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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Quality Assurance Csv Lead
vor 1 Woche
Visp, Schweiz Lonza VollzeitSwitzerland, Visp Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas,...
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Quality Assurance Manager Csv
vor 1 Woche
Visp, Schweiz Lonza VollzeitSwitzerland, Visp Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas,...
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QA CSV Specialist
vor 2 Wochen
Visp, Schweiz Randstad (Schweiz) AG VollzeitJobdescription 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...
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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, 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
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 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...