5 - 8 years
4 - 7 Lacs
Posted:3 hours ago|
Platform:
Work from Office
Full Time
1. Sampling of raw material, packing material, intermediates, APIs as per approved sampling plan.
2. Carry out analysis of raw material, finished product and packing material as per approved specifications & Method of analysis.
3. Preparation and maintenance of volumetric solutions, reagents, buffers and chemicals.
4. Perform Calibration of QC Instruments and maintain records.
5. Preparation of analytical method transfer and analytical method validation protocols.
6. Perform Analytical method transfer/Analytical Method validation related activities.
7. Prepare Standard operating procedures and to train concerned staff.
8. Preparation of Analytical Protocols, Specification and Method of analysis.
9. Preparation and execution of IQ/OQ/PQ documents as per CVG/CSV SOP’s.
10. To coordinate with R&D team and ensure completion of Analytical Method Validation/Transfer of a product before start of campaign.
11. Preparation of COA as per requirement.
12. Working /Reference/In-house standards and Impurity management.
Solara Active Pharma Sciences
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