Cadila Pharma

Principal task:
1) To developed Analytical Method Development, Routine analysis and Validation, by GC &
GCMS.
2) To take care of CSBU projects of Analytical Method Development and Validation, Method
Transfer and Regulatory Queries by GCMS, and GC with scientific guidance.
3) To maintain and observe GLP in working environment in GC.
4) Timely respond development of the Regulatory Queries of products.
Responsibilities:
1) Preparation of New Analytical method validation and Method Transfer Protocol and Report as per the current Regulatory requirement.
2) Prepare Protocol of analytical method validation and method transfer report and routine analysis data.
3) Preparation of standard operating procedure.
4) Maintaining GC calibration report.
5) Trouble shooting during day to day analysis with proper instrument care.
6) Taking care of PM of all the instrument of Analytical GC.
7) Ensure the compliance in Lab.
8) To close the change control and incidence

Job Details

Skills Required

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