1) Responsible for complete life cycle management of approved products 2) Compilation, update & Review of Clinical-Non-clinical part of the EU registration dossier [Module 2.4-2.7, Module 4 & 5] 3) Periodic /timely review & update of product information [SmPC, PIL & Labelling] 4) Review, update & approval of commercial artworks, print-proofs & change control. 5) Timely update of in-house regulatory software & XEVMPD database. Job Type: Full-time Salary: ?429,884.97 - ?1,454,482.11 per year Schedule:
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