QA Specialist, CSV
vor 1 Woche
Join to apply for the QA Specialist, CSV & Automation role at JobCourier . We are seeking an experienced QA Specialist, CSV & Automation to support large‑scale CAPEX projects within a GMP‑regulated manufacturing environment for our pharmaceutical client based in Visp . Responsibilities Ensure qualification/validation plans and execution for equipment, infrastructure and computerized systems are in place in accordance with Lonza Quality policies. Approve SOPs, commissioning/qualification/validation protocols and reports, and project‑related CSV documents (e.g., URS, FAT/SAT). Provide QA leadership, oversight and support to staff on qualification/validation topics related to ongoing projects and ensure selected vendors are qualified. Act as the first point of contact within GQE for any area related to the lifecycle and compliance for equipment, infrastructure and computerized‑systems qualification/validation, including documentation in shared global systems (e.g., Kneat, Trackwise, DMS, Unifier). Manage quality deviations, changes and CAPAs/tasks in a timely manner, taking leadership for their resolution and escalating when necessary. Qualifications Bachelor or Master’s degree in Engineering, Life Sciences or related field. Significant experience in the GMP‑regulated pharmaceutical industry, preferably in a role within a Quality Unit. Experience in a QA role for the CSV/Automation of GMP systems related to aseptic fill‑finish processes and facilities (filling equipment, lyophilization, clean utilities, and clean room facilities). Fluency in English; German would be an advantage. Location: Visp, Valais, Switzerland (may be remote) Contact: Alba Jansa – – Seniority level: Mid‑Senior level. Employment type: Full‑time. Job function: Quality Assurance. #J-18808-Ljbffr
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QA CSV Specialist
Vor 5 Tagen
Visp, Valais, Schweiz Gi Group VollzeitQA 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 Specialist, CSV
vor 4 Wochen
Visp, Schweiz Experis Switzerland VollzeitJob Title QA Specialist, CSV & Automation Job Description 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....
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QA Specialist, CSV
vor 1 Woche
Visp, Schweiz Experis Switzerland VollzeitJob Title QA Specialist, CSV & Automation Job Description 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....
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QA Specialist, CSV
vor 2 Wochen
Visp, Schweiz JobCourier VollzeitJoin to apply for the QA Specialist, CSV & Automation role at JobCourier.We are seeking an experienced QA Specialist, CSV & Automation to support large‑scale CAPEX projects within a GMP‑regulated manufacturing environment for our pharmaceutical client based in Visp.ResponsibilitiesEnsure qualification/validation plans and execution for equipment,...
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QA CSV Specialist
Vor 2 Tagen
Visp, Valais, Schweiz Adryan VollzeitJob Description: QA Computer System Validation (CSV) SpecialistDuration: 1 year contractLocation: VispSummaryThe QA CSV Specialist is responsible for establishing and enhancing best practices for Computer System Validation (CSV) within the framework of current GAMP and international regulatory guidelines. The role includes both strategic development of CSV...
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QA Specialist, CSV
Vor 7 Tagen
Visp, Valais, Schweiz Experis Switzerland Vollzeit: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...
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QA Specialist, CSV
Vor 6 Tagen
Visp, Schweiz Experis Schweiz VollzeitFor 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...
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QA CSV Specialist
vor 2 Wochen
Visp, Valais, Schweiz Hays VollzeitTheQA 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...
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GMP QA: CSV
vor 2 Wochen
Visp, Schweiz JobCourier VollzeitA pharmaceutical engineering company in Visp is looking for a QA Specialist, CSV & Automation. This full-time role involves supporting large-scale CAPEX projects in a GMP-regulated environment. The ideal candidate will have a degree in Engineering or Life Sciences, significant experience in the pharmaceutical industry, and leadership capabilities in QA. The...
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GMP QA: CSV
vor 1 Woche
Visp, Schweiz JobCourier VollzeitA pharmaceutical engineering company in Visp is looking for a QA Specialist, CSV & Automation. This full-time role involves supporting large-scale CAPEX projects in a GMP-regulated environment. The ideal candidate will have a degree in Engineering or Life Sciences, significant experience in the pharmaceutical industry, and leadership capabilities in QA. The...
