Executive
Cadila Pharmaceuticals Ltd
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Posted: 13 Jun 26
Job 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."
• 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."
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2906630
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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