Executive

Cadila Pharmaceuticals LimitedDholka, GujaratOn-siteFull-timeMid level, 2–5 yearsListed 6 hours ago

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About this role

"Follow cGMP and GLP practices in quality control lab. To prepare Specification Master as per STP in SAP/LIMS. To follow safety Procedure in QC department. Preparation of COA as per current specification for Packing samples (whenever required) To receive the sample for analysis and making entry in inward register/LIMS. To maintain the report within QC Department. To provide the report to QA department for releasing the product. To enter the results in SAP/LIMS for maintain the specification Packing Material wherever required. To do any other Work assign by HOD." Sampling and Microbiological/ chemical testing of Purified water, Water for injection, Potable water samples and pure steam condensate samples. Plate / Tube verification and release and on-line data recording Work allocation and distribution To ensure the training about the changes in standard operating procedures (SOP), if required. Review of analytical data Change control, master document preparation and review Regulatory Audits and Periodic self-inspection Do any other Work assign by HOD."