August 2024

M. Pharm M.S. in Natural Products. Pharmaceutical Chemistry, Medicinal Chemistry or equivalent degree from a recognized University or equivalent. or M.Sc. in Organic Analytical Chemistry. Phytopharmaceutical Mission Phase III

B.Pharm OR D.Pharm with working experience in Dispensary, Pharmacy of the Hospital having minimum 200 beds. Registration with State Pharmacy Council with duly allotted Registration Number is mandatory. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India. TMC is affiliated to Homi Bhabha National Institute.

Doctoral Degree in Science, Engineering, Technology, Pharma, MD, MS from a recognized University or equivalent. Genetic and transcriptomic insights into anti-pathogenic activity and ecology of Xanthomonas sontii, a non- pathogenic species of rice microbiome

responsible for providing Specialized Service such as IP management, Technology Transfer, Technology Acquisition and to ensure their execution assuring highest quality. In addition he, she will provide support to all HR and Administrative matters of the Company which include recruitments, managing the Contracts, day-to-day administration, management of meetings, conferences and events, procurement matters and HR policy.

Ph.D Tech in Pharmacy Pharmaceutics, Pharmacology, Pharmcognosy and Pharmaceutical Chemistry; Online applications are invited for the following Ph.D. Tech. / Ph.D. Science programmes at ICT Mumbai, ICT-IOC Bhubneswar and ICT Marathwada Jalna campuses.

To perform investigation for Deviation, OOS, OOT observed at plant.Preferably to have regulated market Science based scale up factor based Tech transfer experience.

Collaboration with R&D and other stakeholders to enable timely filing and review of documents for EU, UK, CA, AUS for solid oral and topical dosage forms RA strategy in collaboration with partners with focus on cost implications.

Experienced in qualification documents preparation i.e. protocol preparation. Risk assessment, technical documents review and execution. Hands on experience on QMS - investigation, change control, impact assessment: Drafting and review.

Compile registration dossiers for submission to various health authorities like – US, Canada, Europe, Australia. Prepare responses to deficiency letters received from various agencies.