M.Pharm

Develop detailed project budgets, including cost estimates. Monitor project expenditures and ensure adherence to budgetary constraints. Develop project timelines and schedules, identifying critical milestones and dependencies. Also Monitor progress against timelines and implement adjustments as necessary to ensure on-time delivery

Analytical method development, stability samples analysis and impurities identification and characterization with hands on experience in HPLC, GC, LC-MS, GC-MS, ICP-MS and other analytical techniques. Preparation of analytical method development reports, validation protocols and reports in accordance with guidelines.

Experience in into HVAC, Calibration,Utility Electrical, Documentation, Finished Goods, Raw Material, Stability, Dispensing & receipt of Raw Material & Packing Material

Evaluation of immunomodulatory and anti-cancer properties of Hydroxychavicol, a major constituent of Piper betel. Perform the project related experiments, develop new techniques and protocols for drug screening using cell culture technology.

M.Sc or M.Pharm. Coordinate with all concerned department to ensure timelines and compliance to regulatory or sponsor requirements for preparation, compilation and delivery of reports. Electronically generate, review study documents and submission of study reports in CTD/eCTD format as per regulatory requirements.

The incumbent would need to build a strong New Product Portfolio and its management and delivery in a time bound manner for India Business of Sun. Works closely with the Business/Marketing, Business Development, R&D, Manufacturing, Regulatory, IP, Market Research, SFE, CEO Office, Commercial, Medical, Clinical Research, CQA, Finance, PMO, New Product Launch, Network Strategy, Packaging development teams etc.

To develop approaches for Downstream processes, designing and managing multiple process development projects; to take up new technology initiatives within the downstream development group. To draft primary documents for functional deliverables.

Provides critical support and coordination in the review of safety and regulatory publishing documents, ensuring timely and accurate processing upon receipt. Plays a key role in maintaining document quality by tracking safety and regulatory publishing data, ensuring seamless uploading into internal and/or external electronic trial master files.