1. Hands on 12 -15 years experience on HPLC, UPLC, Dissolution, UV, IR and Wet Analysis.
2. Exposure on Analytical Method Development and Analytical Method Validation for Solid Dosage Forms, sterile, eye drops and topical dosages forms and troubleshooting in analytical methods for the same & reporting the documents.
3. Should have a prior experience in Analytical Method Transfer activities.
4. Should have awareness on good documentation practices and comply with EU / USFDA regulations. Generation of validation protocols, development reports, stability & Departmental SOPs.
5. Should be up to date with regulatory requirements and Guidelines.
6. Perform and assist in Method. Dev and Method Validation
7. Perform routine analysis to support product Development.
8. Write or assist in preparation of analytical protocols and reports.
9. Must be capable of maintaining clear and consistent laboratory records.