Intern - QA Specialist Batch Record Review — Lonza

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Descrizione completa

The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation. This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation control, and compliance with internal procedures and regulatory standards. The intern will work closely with QA specialists and cross‑functional teams to ensure timely and accurate batch record processing. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get:

  • An agile career and a dynamic work culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance. What you will do:
  • Review of the Executed Batch Records (e.g. cleaning logs, production documentation review, temperature reports, test procedures, raw data, logbooks)
  • Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
  • Support the initiation of deviations and investigations for Batch Record review related observations What we are looking for:
  • Bachelor degree or relevant work/ internship experience in Biology, Chemistry, Biotechnology, Life Science or other related field
  • Previous experience in GMP regulated pharmaceutical / API industry is an advantage
  • Ability to identify non-compliance and gaps from quality standards
  • Structured, precise and well-organized working attitude; open-minded for new ideas and suggestions; agile, highly motivated and dynamic drive
  • English: Fluent. German: Good to have. 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. Lonza is a global leader in pharma and biotech manufacturing. The company operates major production facilities in Visp (Valais), Basel, and Stein (Aargau), Switzerland.

Dettagli dell'offerta

  • Azienda: Lonza
  • Posizione: Intern - QA Specialist Batch Record Review
  • Sede: CH, Ticino
  • Stipendio: CHF 49'500 - 66'500 (fonte non verificata)
  • Settore: Farmaceutica / Biotecnologia
  • Scaduta il: 2026-07-23

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