About GSK :
The company has more than 100 years of history which established long back around late 1800. This is one of the leading pharmaceutical company in India.
Company has numerous NDA and ANDA with API filings across Europe, south Africa, Canada, Brazil and Australia. Company emphasis on upcoming technology and has many formulation research based centers, with 150 bed bioequivalent centers around Vadodara, and Gujarat. Initiated state of art R&D center in Hyderabad. Firm is investing around 11% of its profit in its R&D Operation.
Company has pipeline in Oncology products, dermatology, auto immune disorders and injectable formulations.
About the Job :
Experience : Candidate should have masters with exposure in regulated environment in DP development
and in the field of CMC and labelling and legislative requirements
Job role :
Need to collect the data and deliver the action items with in the timelines as per the regional and global agreements
Need to work closely with IT team
Need to identify the global regulatory affairs procedures and update them