Posted:3 months ago|
Platform:
Work from Office
Full Time
1. Testing of Samples.
2. Handling instruments such as HPLC, GC, UV Spectrophotometer, etc.
3. Development of Analytical methods for various formulations.
4. Validation of Analytical methods.
5. Preparing analytical method development reports.
6. Method Transfer.
7. Literature survey for existing analytical methods on Internet.
8. Carry out literature survey by establishing the strategies.
9. Pre-formulation sample analysis. (Solubility, Force-degradation, photo stability etc.)
10. Drug Excipient Compatibility Sample Analysis.
11. Trial batch Analysis.
12. Trial batch Stability sample analysis.
13. Reference product Analysis.
14. Prepare cGLP/cGMP documents.
15. Maintenance of reference standard, working standards and their standardization.
16. Coordinating the activities in Chemical and Instrumentation.
17. Analytical Method Development and handling of Troubleshooting.
18. Preparation and Review of Raw Material, Packing Material, Finished Product Release Specification and Standard Test Procedure. Analysis of Raw Material, Packing Material & Finished Products. Performing quality control activities as per daily analysis plan.
Avery Pharmaceuticals Pvt. Ltd
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