Description

• Development of Lyophilized Complex/Peptide Injectable & Biosimilar Product Development (Thaw, filter, fill & Finish).
• Drug Product R&D Stability, Compatibility & Development Studies.
• Participate in scale-up, toxicity/clinical exhibit batches of the Drug Products under development.
• Authoring regulatory filling & TTD Documents i.e. MF, RA, PDR, Stability Study Plan & R&D Stability Studies.

Qualifications

M.Pharm - Pharmaceutics

Experience

Tenure : 2-6 years