Senior QA Specialist
vor 2 Wochen
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. What you will get: An agile career and a dynamic work culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below. Benefits in Visp: What you will do: Take ownership of quality-related activities for Microbial manufacturing processes and Master Cell Banking (MCB) Responsible for review and final release of records (QMS, SOPs and GMP documentation) Provide guidance to stakeholders and ensure compliance with cGMP through risk assessments and proactive identification of non-conformities Primary QA contact for contamination prevention and control strategies across microbial operations and collaborate with local and global teams to share best practices Represent QA during customer audits and regulatory inspections, and actively participate in internal audits Drive continuous improvement projects to strengthen quality and regulatory adherence What we are looking for: Academic degree in Life Sciences (Microbiology / Biotechnology, or a related field) Profound experience in a GMP regulated environment, preferably withing QA/QC Strong communication skills and ability to collaborate effectively with colleagues across different functions Proactive, detail-oriented mindset with a focus on continuous improvement and problem-solving Excellent verbal and written communication in English. German language is a plus About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now. Reference: R71489
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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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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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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 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 Specialist 100 %
vor 4 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 2 Tagen
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...
