September 2025

The candidate must have a Diploma in Pharmacy from the State Board of Technical Education or a Degree in Pharmacy from a recognized University. (Preference will be given to those with a degree in Pharmacy.)

B.Pharm and M.Pharm in the relevant specialization with first class or equivalent in any one of the two degrees.

Masters degree in pharmacology, Pharmaceutics, Pharmaceutical Regulatory Affairs, and Biotechnology.

M.Sc in life sciences, PG diploma in Clinical Research and Pharmacovigilance 

As a PPD FSP Clinical Research medical Advisor you may support a variety of designated therapeutic areas including Cardio-Renal-Metabolic/Immunology/Neuroscience.

Participation in Trade Association calls in listening & learning, observer mode by leveraging the discussion and lessons learnt onto CMC Regulatory Intelligence databases.

Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information, in line with regulatory requirements and the agreed strategy defined by the cross functional team

The incumbent will be responsible for performing analytical method development and validations for USP/NF monographs and maintaining safety and GLP environment in the lab.

Review of Product Quality Complaint Investigation Reports Drug Products.Coordinate with other stakeholders involved in the complaint handling process.