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Enzene Biosciences Ltd. is seeking an experienced QC professional to plan analytical studies for DS, DP, and stability samples and to review data for routine analyses.
The role includes preparation and review of controlled documents such as Specifications, STPs, TDS, SOPs, CoAs, and method validation plans, while managing QC reference standards and consumables to support reliable QC activities.
Responsible for analysis planning of DS, DP, Stability and protocal based samples.
Responsible for review of analytical data for routine samples.
Responsible for management of reference standard in Quality Control Dept
Responsible for preparation and review of documents like Specificaiton, STPs, TDS, SOP, CoA, MTP, MVP, MVR, MTR.
Responsible for inventory management of QC consumable items
Qualification : MSc, MPharm
Experience : 10 to 12 years of experience in the task such CEX-HPLC, SE-HPLC, RP-HPLC, ELISA, Maurice system