Will be responsible for effective and smooth Technology Transfer of various dosage forms for regulated market.
Managing projects focused on various techniques .
To Ensure the transfer of project with proper manufacturing process (BMR), Protocols,
Analysis and planning of the Holding time for transfer the project from development of dosage forms like, Tablets (Conventional, Modified or Extended release, enteric) MUPS, Capsules & Injections (Liquid and Powder)
Expertisations in solving the FDA queries during filling of the dossier.
Process Optimization & Scale up.
M. Pharma. with similar experience in Technology transfer involving in reputed Pharma R&D.