M.Sc

To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods.

Preparation of additional information or responses as requested by regulatory agencies. Prepare or maintain technical files as necessary to obtain and sustain product approval. Direct the collection and preparation of laboratory samples as requested by regulatory agencies. 

Pharma knowledge of Solid orals & Quality process. USFDA, MHRA, ANVISA & Other regulatory exposure is preferred including ICH guidelines.

Analytical Method development. Handling HPLC, GC, UV IR, KF, Dissolutions

FFS, LVP, Flow wrapping, SHWSS, Terminal Sterilizer, Dry powder injection, Injection Labelling, Capsule Filling, Compression, Granulation, Coating

Post Graduate, Graduate, Diploma in Pharmacy, Commerce, Science

Lead the assessment of existing ecosystems across key pillars, including client portfolio plans & objectives, technical architecture, data models etc. Collaborate with cross-functional teams to design and implement the optimal solution, ensuring seamless integration with existing processes

Responsible for fund disbursal to the selected applicants under the scheme based on the parameters and milestones as set by the implementing authority. Preparation of agenda items for meetings of the Committees set-up under the scheme, and providing secretarial assistance to DoP for the same.