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
#J-18808-LjbffrTablet Packaging Documentation Lead — GMP & Compliance in Worthing employer: GlaxoSmithKline
GlaxoSmithKline is an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the pharmaceutical industry. With a strong commitment to employee development, you will have access to numerous growth opportunities while enjoying a competitive salary, annual bonus, and a flexible hybrid working model that promotes work-life balance. Located in the UK, GSK's culture prioritises teamwork and inclusivity, making it a rewarding place for professionals passionate about making a difference in healthcare.
