Senior QA Specialist
vor 3 Wochen
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 will work closely with quality, engineering, and operational functions to ensure cGMP‑compliant manufacturing and documentation. What You’ll Get An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. A variety of benefits dependent on role and location. What You’ll Do Coordinate QA interests during different project phases. Responsible for project‑specific QA operation tasks during commissioning and qualification. Responsible for review and final release of records such as SOPs, Master Batch Records, Material Specifications, Quality Risk Assessments, Deviations, CAPAs, Change Requests, Effectiveness Checks, Testing Protocols & Reports. Manage stakeholders and their needs independently in a customer‑focused environment. Participate and support regulatory inspections and customer audits. What We’re Looking For Bachelor’s or master’s degree in biotechnology, biochemistry, or a related field. Significant experience in biopharmaceutical manufacturing, preferably in a QA function. Strong background in cGMP and broad knowledge of biotechnological manufacturing processes, validation approaches, and risk management. Sound experience representing quality and compliance in projects. Good communication skills and experience interacting with all interfaces within the organization. Experience with TrackWise, LIMS, DMS, and SAP preferred. Excellent written and spoken English. Knowledge of German is an advantage. Our products and services have a positive impact on millions of people. We respect and protect our people and environment, and we expect all employees to act ethically. Lonza is an equal‑opportunity employer. All qualified applicants will receive consideration without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability status, or veteran status. Reference: R71290 Apply #J-18808-Ljbffr
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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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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 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 Specialist 100 %
vor 3 Wochen
Visp, Schweiz Careforce24 VollzeitIn 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...
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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 Analytics Lead — GMP, Data
vor 3 Wochen
Visp, Schweiz Lonza VollzeitA leading life sciences company in Visp, Switzerland, is seeking a Senior QA Specialist to ensure quality oversight on GMP-relevant activities. The role involves reviewing and approving SOPs and analytical methods to ensure compliance with standards. Ideal candidates will have a degree in Chemistry or related fields, along with significant experience in the...
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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
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...
