Analytical Method development and report preparation on LCMS/MS (for Nitrosamine impurities,
azido impurities etc.)
Analytical methods validation and report preparation on LCMS/MS (for Nitrosamine impurities,
azido impurities etc.)
Routine and stability sample analysis.
Analytical method verification of drug products and drug substances on LCMS/MS.
Documentation as per the GLP requirement.
Maintain GLP in the laboratory as per regulatory requirement.
Analytical Method transfer to QC Lab
Taken care of laboratory equipment and breakdown.
Routine analysis and stability sample analysis.
Maintain cleanliness in Lab.
To develop analytical method for drug substances and drug products on LCMS/MS.
Review of analytical reports.
Review of analytical data.
📌 Deputy Manager (Dholka)
🏢 Bioksha
📍 Dholka
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