Lonza in Visp, Switzerland is seeking a motivated Intern for QA Documentation Support. In this fully site-based role, you will collaborate with cross-functional teams to ensure manufacturing activities meet cGMP compliance standards.

Key responsibilities include reviewing Batch Records, supporting batch release, and drafting SOPs. Ideal candidates hold a degree in a relevant field and possess proficiency in English. Join us at Lonza to contribute to the future of life sciences.