Responsible for safety monitoring and evaluation of assigned GSK products. Conduct safety monitoring and evaluation for assigned products, including signal detection and risk assessment.
Masters degree in Chemistry or Biochemistry or Pharmacy or Pharmaceutical Chemistry or Pharmacology or Bacteriology or Medicine or Microbiology or Biotechnology of a recognised university or institute.
Bachelors degree in life sciences, pharmacy, or a related field. An advanced degree is preferred. Extensive experience in pharmacovigilance or drug safety reporting, with a strong understanding of relevant regulations and guidelines.
BS degree in Pharmacy or Life Sciences or relevant education. Minimum 1 year of relevant experience in regulatory affairs, quality or product development in the pharmaceutical, medical devices or similar FMCG industries.
M.Tech / M.S (Pharm) / M. Pharm / MSc in Pharmacy / Nanotechnology from a recognized University with sound knowledge in the application of nano formulations in drug delivery plus GPAT/GATE/NET/ any national- level entrance test, qualified
Post Graduates in Life Sciences / Pharmacy/Statistics/Social works/ Sociology/BAMS,BSMS and MD in AYUSH with at least 55% marks with one year of post qualification experience in the related field.
Handling the Incidents / Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory.
Supports to the Laboratory functions to handle Investigations, Deviation Management, Specifications ,test methods, method validations equipment qualifications ,internal audits and escalations if any.