Job Overview
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Date PostedJanuary 27, 2023
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Location (State / UT)
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Expiration date--
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Experience3 Years, 6 Years
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GenderAny
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Desired QualificationMaster’s Degree
Job Description
Execute end-to-end formula and process development of products following good laboratory practices and continuously monitor its data and quality to have a robust effect within the budget, timeline, and regulatory standards
Key Accountabilities
- Collate and review Pharma literature from USFDA etc. in order to utilize knowledge during product development
- Provide and submit all stage gates documents to CFT on the basis of data generated from development trials to execute batches at the plant
- Gather data from pre-formulation studies by carrying out the characterization of the reference products and optimize the formula in order to develop a robust product
- Provide indent through supply chain management to procure the Filters, RM and PM required during product development and submission batches
- Prepare regulatory submission data by conducting R&D trials and executing regulatory submission batches at the unit for successful filing
- Provide deficiency response support by generating data at R&D/Unit required for approval of the product
Education Qualification
Master in Pharmacy (Specialization in Pharmaceutics)
Relevant Work Experience
- 3-6 years experience in R&D