Technical SupervisorJobs Opening in Cadila Pharmaceuticals Ltd at Dholka
Technical Supervisor
Cadila Pharmaceuticals Ltd
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Posted: 13 Jun 26
Job Description
• Follow cGMP and GLP practices in Quality Control Lab.
• To analyze the Sample of In process validation and finish product on non-chromatographic instrument such as FTIR, UV, Dissolution, DT , Hardness etc by following test procedure.
• To attend the training as per schedule.
• To follow safety procedure in qc department.
• To receive the samples for analysis and making entry in Inward register.
• To maintain the Instruments log books related to sample analysis.
• To analyze the sample and compilation of documents.
• Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS.
• Responsible for cleaning & monitoring of laboratory.
• Responsible for online documentation.
• 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.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2906674
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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