Job Overview
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Date PostedJanuary 14, 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 product within the budget, timeline, and regulatory standards
Accountabilities
- Collate and review Pharma literature from USFDA etc. in order to utilize knowledge during product development
- Plan the device development and ensure implementation and execution of related activities within a predefined time for the successful completion of quality products
- Review & analyze all the design development documents viz. design development plan, design input (URS), design output, design verification, design validation, and design transfer, etc. to maintain quality & regulatory standards
- Ensure timely delivery of projects by assessing and mitigating the risk involved in various stages of the projects
- Design review meeting with CFT and component vendor.
Education Qualification
M.Pharmacy, Ph.D
Relevant Work Experience
3 -6 Years in R&D