2 – 5 Years
Having an overview on GAMP requirements related to control system & IT systems.
Support in establishing compliance related to CSV like data integrity, RERS etc.
Able to participate in execution and review process of all qualification documents during testing phase like IQ, OQ & PQ stages of project.
Able to assist and review the requirements mentioned in the Validation plan to complete the validation summary reports.
Act as core support in completion of qualification documentation between cross functional teams.
Having good oral & written communication skills.
Please note this a contract role for 12 months period.
PG – M.Tech – Any Specialization, M.Pharma – Pharmacy
Doctorate – Doctorate Not Required
GSK is one of the world’s leading research based pharmaceutical and healthcare companies. GSK will be investing up to INR 1000 Crores (Â£100m) in a new ‘state of the art’ pharmaceutical factory in Vemgal (45 KMs away from main city), Bengaluru. The factory will initially supply a range of solid dose form products. After completion of the project, the factory will produce more than 9 Billions tablets and capsules per year, supplying the Indian market with product, with production ramp-up through 2017. The factory is being built to the highest international standards using the latest process technology.
GSK intends to create an environment where development of staff is key, where people delight in where they work and are inspired to deliver their best. A modern way of working will be created where people are valued for the contribution they make and where their career aspirations can be met.
This is an exciting development for GSK and the new factory at Vemgal aims to be recognized as a ‘benchmark’ operation.
To know more about our organization please login to www.gsk.com, www.gsk-india.com