Found Description
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:
What you will do:
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