Full-time
QA Batch Record Review Intern: GMP Compliance
Posted by Lonza • stalden (vs), wallis, Switzerland
About the Role
Lonza in Stalden (VS), Switzerland is seeking an Intern - QA Specialist for Batch Record Review. This role supports the Quality Assurance team by reviewing and verifying GMP manufacturing documentation, ensuring compliance with regulatory standards.
The ideal candidate will have a Bachelor degree in a relevant field and strong organizational skills. The position offers hands-on exposure to regulated practices, teamwork opportunities, and a dynamic work culture.
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