Cadila Pharmaceuticals
Technical Supervisor
- Compensation
- Not disclosed
- Location
- Dholka
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- Not specified
- Category
- Not specified
- Posted
Full description
- 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.
- 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.
- 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.