Principal task: 1) Monitoring Analytical method development, Validation study and method transfer activities.

- Review the analytical method development data, validation study data and method transfer protocol and reports.
- Preparations of justifications 4) To maintain and observed GLP/GDP in working setting.
- Investigation Study as per requirement.

Responsibilities: 1) Review of analytical method validation and method transfer protocol and report as per the current regulatory requirement.
- Review Regulatory Queries of product receiving form different regulatory agencies.
- Preparation and review of standard operating procedure.
- Maintaining HPLC calibration report.
- Trouble shooting during day-to-day analysis with proper instrument care.
- Taking care of Analytical HPLC Spare.
- Maintain records for all analytical reports by entering all the data and timely release the analytical reports to concern dept.
- Maintain Coordination with Plant site during Method transfer activity.

📌 Research Associate - II (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka