B.Pharm

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.

B.Pharm with experience in Oral Liquid manufacturing. Should have good knowledge of documentation and qualification activities. Liquid Approved is desirable.

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.

Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world.

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

The applicant needs to attend the Walk-in-interview on the scheduled date & time. Any delay will not be entertained any point of time.

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.