Principal task: 1) To maintain and observe GLP in working setting in GC.
- Timely respond development of the Regulatory Queries of products.
- Preparation of COAs Responsibilities: 1) Preparation of New Analytical method validation and Method Transfer Protocol and Report as per the current Regulatory requirement.
- Prepare Protocol of analytical method validation and method transfer report and routine analysis data.
- Preparation of standard operating procedure.
- Maintaining GC calibration report.
- Trouble shooting during day to day analysis with proper instrument carc.
- Taking care of PM of all the instrument of Analytical GC.
📌 Research Associate (Dholka)
🏢 Cadila Pharmaceuticals
📍 Dholka
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.