EDUCATION: M.SC / B.SC/ M.Pharm/ B.Pharm
Design, execute and interpret formulation and process development experiments with Quality by Design concept leading to the solid oral pharmaceutical dosage forms (IR and modified release) for(Para II, Para III & ROW Para IV) and WHO Geneva.
* Execution of scale-up batches like Pre-exhibit, Exhibit (Submission batches) and PV batches.
* Generation & review of scale-up and regulatory submission documents
* Resource organization & co-ordination with relevant departments viz. ADL, R&D - QA, Regulatory, Commercial, Manufacturing and Engineering etc.