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Tatva Chintan Pharma Chem logo
Assistant Manager - DQA Tatva Chintan Pharma Chem

5.0 - 10.0 years

4 - 8 Lacs

vadodara

Work from Office

Should understand and have hands on experience on the preparation and documentation of below subjects required for new and existing products during development, scale up & commercialization: Literature search report Feasibility Report Optimization Report / Lab Validation report/Standard laboratory process etc. Demo Report / Scale up report etc. Technology Transfer Document Trend Analysis in Synthesis and Quality Analytical Method Development, specs/STP/STDs/INT & validation Root of synthesis, Process Flow New ADL methods / Analytical Method Transfer protocol/Stability Studies protocol. SOP / BMR / BPR Stability report study Interacting closely with R & D and ADL to develop new documents & tr...

Posted 1 week ago

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