QA Specialist

vor 1 Woche

Visp, Schweiz Lonza AG Vollzeit CHF 60'000 - CHF 90'000 pro Jahr

Location: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

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, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

We are looking for a QA Specialist (f/m/d) to join multinational QA Operations team in the Bioconjugates Business Unit at the Visp site. You will work closely with various quality and operational functions to ensure GMP-compliant manufacturing and documentation. You will also get exciting insights into our IBEX environment and can develop into QA project management role in perspective.

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 dependant on role and location

The full list of our global benefits can be also found on

What you'll do:

  • Review executed electronic and/or manufacturing protocol for compliance to GMP

  • Review and support of review and release of master manufacturing protocols / electronic master recipes for GMP manufacturing

  • TrackWise record management (e.g: CAPAs)

  • Ensure that internal/ external GMP standards and regulatory requirements related to process validations are adhered to in projects

  • Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures

  • Participate on disposition package preparation according to internal and customer requirements

  • Participate and support regulatory inspections and customer audits. Represent the Quality Unit in cross-functional teams

What we're looking for:

  • Academic degree in Biology/ Chemistry/ Biotechnology, Life Science or other related field

  • Previous experience in GMP regulated pharmaceutical industry is required

  • Fluent English is required, good command of German is an advantage

  • Ability to prioritize and manage work to critical project timelines in a fast-paced environment

  • Excellent verbal, written and interpersonal communications skills

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

  • eBR (Electronic batch record) Reviewer QA / OPs

    vor 2 Wochen

    Visp, Schweiz QA Vollzeit

    eBR (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...

  • QA Specialist 100 %

    vor 3 Wochen

    Visp, Schweiz Careforce24 Vollzeit

    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...

  • QA CSV Specialist

    vor 1 Woche

    Visp, Schweiz Gi Group Vollzeit

    QA 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...

  • Senior QA Specialist, cGMP Biopharma

    vor 2 Wochen

    Visp, Schweiz Lonza Vollzeit

    A 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,...

  • QA CSV Specialist – 6760 ASH

    Vor 2 Tagen

    Visp, Schweiz CTC Resourcing Solutions Vollzeit

    CTC 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...

  • QA CSV Specialist

    vor 2 Wochen

    Visp, Valais, Schweiz Gi Group Vollzeit CHF 90'000 - CHF 120'000 pro Jahr

    QA 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...

  • QA CSV Specialist

    vor 3 Wochen

    Visp, Schweiz Proclinical Group Vollzeit

    Do 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...

  • QA CSV Specialist

    vor 1 Woche

    Visp, Schweiz Proclinical Staffing Vollzeit

    Do 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...

  • QA CSV Specialist

    vor 3 Wochen

    Visp, Schweiz Actalent Vollzeit

    Join 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...

  • QA CSV Specialist

    vor 2 Wochen

    Visp, Schweiz Randstad (Schweiz) AG Vollzeit

    Jobdescription 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...