Intern QA Documentation Support

vor 20 Stunden

Visp Valais, Schweiz Lonza Vollzeit

Switzerland, Visp

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're expanding our team in Visp and are currently seeking a motivated Intern for QA Documentation Support (m/f/d). In this role, you'll report directly to the QA Operations Group Leader and collaborate closely with cross-functional teams in Quality and Operations. Your mission: to help ensure that our manufacturing activities and documentation meet the highest standards of cGMP compliance.

What You'll Get

  • A dynamic, agile career path with room to grow
  • An inclusive, ethical, and supportive workplace culture
  • Performance-based compensation programe
  • A comprehensive benefits package tailored to your role and location

*What you'll do:*

  • Conduct thorough reviews of executed Batch Records, including production documentation, test procedures, raw data, and logbooks
  • Support batch release by verifying the completeness and accuracy of documentation packages
  • Analyze and clarify comments within Batch Records in collaboration with Operations and the responsible QA Manager
  • Assist in initiating deviations and investigations related to Batch Record observations
  • Regularly collect and assess KPI data to support continuous improvement
  • Draft and update SOPs within your area of expertise

**What we are looking for:****

  • A degree in Biology, Chemistry, Biotechnology, Life Sciences, or a related field
  • Structured, detailed and well-organized working attitude; open-minded for new insights and suggestions; agile, highly motivated and dynamic drive
  • Proficiency in English (required); German language skills are a strong plus

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.

Reference: R70414

Apply

Similar Jobs

R70567

R71273

  • 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 Batch Record Reviewer

    vor 2 Wochen

    Visp, Valais, Schweiz CTC Resourcing Solutions Vollzeit CHF 60'000 - CHF 90'000 pro Jahr

    QA Batch Record Reviewer - 6767Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is recruiting for a talentedQA Batch Record Reviewer to be based in Visp, Switzerland.QA Batch Record ReviewerLocation: Visp, SwitzerlandContract Duration: to possibility...

  • QA Batch Record Reviewer

    vor 2 Wochen

    Visp, Valais, Schweiz Actalent Vollzeit CHF 60'000 - CHF 90'000 pro Jahr

    QA Batch Record ReviewerLocation:Visp, SwitzerlandStart Date:01 January 2026 – 30 September 2026Workload:100%Language:English (C1), German skills preferredAbout the RoleWe are looking for aQA Batch Record Reviewerto join a leading life sciences organization in Visp. In this role, you will ensure compliance and accuracy of production documentation,...

  • QA CSV Consultant

    Vor 3 Tagen

    Visp, Valais, Schweiz Consultys Suisse Vollzeit CHF 80'000 - CHF 120'000 pro Jahr

    We are looking for a QA CSV Specialist to join our teams in Visp and support the Quality Assurance department in ensuring robust validation and lifecycle management of computerized systems.Your ResponsibilitiesServe as the primary QA CSV representative, acting as a liaison between QA and internal/external stakeholders to ensure clear alignment on CSV...

  • 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 Batch Record Reviewer

    vor 2 Wochen

    Valais, Schweiz BioTalent Vollzeit CHF 60'000 - CHF 90'000 pro Jahr

    QA Batch Record Reviewer – Pharmaceuticals9 month contract - Valais.Open to Swiss residents + EU Citizens who can relocate.Onsite (2 days home office possible)BioTalent looking for a detail-oriented Batch Record Reviewer to join our team and help ensure every batch meets strict GMP and regulatory standards.What you'll do:Review Executed Batch Records...

  • QA Batch Record Reviewer 100%

    vor 2 Wochen

    Visp, Schweiz Careforce Vollzeit

    Key Responsibilities Review executed batch records including production documentation and raw data Ensure full and accurate documentation to support batch release Clarify record comments with operational teams and assess with the responsible QA Manager Support the initiation of deviations and investigations related to record-review findings Job ID 18408

  • QA Batch Record Reviewer 100%

    vor 2 Wochen

    Visp, Schweiz Careforce Vollzeit

    Key Responsibilities Review executed batch records including production documentation and raw data Ensure full and accurate documentation to support batch release Clarify record comments with operational teams and assess with the responsible QA Manager Support the initiation of deviations and investigations related to record-review findings Job ID 18408

  • QA RP

    vor 19 Stunden

    Visp, Valais, Schweiz NonStop Consulting Vollzeit

    QA Responsible Person (RP) / Commercial Quality Assurance HeadOur client, a leading entity in the pharmaceutical industry, offers a chance to spearhead quality assurance operations within their esteemed organization. They uphold the highest standards of medicinal product safety, efficacy, and quality, making them a cornerstone in the health sector. Dedicated...

  • QA Bath Record Reviewer

    vor 2 Wochen

    Visp, Schweiz Experis Switzerland Vollzeit

    QA Batch Record Reviewer We are looking for a motivated QA Batch Record Reviewer for one of our clients based in Visp. This role ensures that batch records are accurately prepared and compliant with regulatory requirements. Responsibilities Review executed batch records, including production documentation and raw data. Support batch release by ensuring...