Related substance and dissolution by Chromatographic methods) 2. Analytical method validation and method transfer.
- Preparation of specification, standard test procedure, Method development Reports of drug products and excipients.
- Maintenance and upkeep of the GLP documents.
- Maintain GLP workplace.
- To provide timely support in resolving regulatory quires.
- To help and supports site QC investigations
Work Experience
0-5Y
Education
Masters in Analytical Chemistry or Pharmacy
Competencies
📌 Research Associate : IRF Analytical (Pune)
🏢 Lupin
📍 Pune
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