M.Pharm

Experience in Regulatory Affairs, CMC, Manufacturing, Quality Assurance/Control, Process Development, or Analytical Development in the pharmaceutical or biotechnology industry

B.Pharm / M.Pharm; Archival and life cycle management of the CTD, e-CTD submission. Senior Executive Regulatory Publishing eCTD

M.Pharm, B.Pharm, M.Sc ; Analysis and sampling of the drug products, Drug substances, excipients, and water sample.

BPharm, MPharm, Pharm D, or MSc. Regulatory Affairs and Submissions Management.

Masters/ Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences. Or Bachelor s degree in Engineering or Technology or Medicine from a recognized University or equivalent.

Thorough understanding of Quality Control investigations, including Lab Incidents, OOS, and OOT. Relevant experience in Oral Solid Dosage formulations and / or Active Pharmaceutical Ingredient processes.

You will be embedded in our client's study team and have a dedicated ICON line manager to support you. Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports

Ph.D. from a recognized University in subject Pharma, Chemistry, Biochemistry, Biotechnology. Level 11 of Pay Matrix Rs.67,700-2,08,700, 7th CPC Scale.

To conduct situational analysis and field visits for enabling informed decision by the states in implementation of the initiative. To assist states and MoHFW in adoption, customization of the IT based Inventory Management system developed by CDAC and NIC e.g. e-Aushidhi, DVDMS etc.