Tablet Packaging Documentation Lead - GMP & Compliance

GlaxoSmithKline in Worthing is seeking a Tablet Packaging Documentation Specialist to own and improve the tablet packaging Batch Production Records (BPRs) for oral solid dose products, ensuring compliance with updated global packaging standards, GMP and data integrity principles.

The role will design, implement and lifecycle manage hybrid MERP and Veeva batch documentation, coordinating with Operations, MSAT, QA, QP, Supply Chain, Artwork and E2E stakeholders to enable right first time batch