QA Specialist 100 %
vor 3 Wochen
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 qualification documents, and assessing technical change requests. Start Date: 01/06/2025 Duration: 6 Months Key Responsibilities - Act as the QA Qualification representative within project teams for new facilities and projects, ensuring compliance in the qualification of facilities, utilities, equipment, and systems - Coordinate and align diverse QA interests throughout the project lifecycle, including processes and cleaning strategies - Drive the execution of a new qualification strategy, making informed decisions as necessary - Compile, review, and release essential qualification documents such as URS, Qualification Plans & Reports, and DQ/IQ/OQ/PQ Reports while supporting quality risk analysis (e.g., FMEA) - Conduct assessments and approve technical change requests relevant to the qualification of various systems and equipment during different project phases - Represent qualification aspects during audits by customers and regulatory bodies - Lead CAPA initiatives and Effectiveness Checks to ensure timely resolution and appropriate documentation of deviations in Deviation Reports Candidate Profile - Bachelor’s degree in Engineering, Chemistry, Biotechnology, or a related discipline - Extensive experience in qualification processes within the pharmaceutical industry - General knowledge of engineering and manufacturing processes - Proven ability to monitor project execution and identify non-compliance with quality standards - Strong understanding of applicable cGMP regulations is advantageous - Languages: Fluent in German & English #J-18808-Ljbffr
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eBR (Electronic batch record) Reviewer QA / OPs
vor 2 Wochen
Visp, Schweiz QA VollzeiteBR (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...
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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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Senior QA Specialist, cGMP Biopharma
vor 2 Wochen
Visp, Schweiz Lonza VollzeitA 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,...
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Senior QA Specialist, QA Analytics 80-100%
vor 3 Wochen
Visp, Schweiz Lonza VollzeitOverviewSenior QA Specialist, QA Analytics 80-100% (f/m/d) role at Lonza in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Lonza is a global leader in life sciences, focused on people, ideas, and ethical business practices.As a Senior Quality Assurance (QA) Specialist for Analytics, you will...
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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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Senior QA Specialist
vor 3 Wochen
Visp, Schweiz Lonza VollzeitSenior 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...
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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 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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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...
