Executive
Cadila Pharmaceuticals Ltd
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Posted: 03 May 26
Job Description
• Follow cGMP and GLP practices in Quality Control Lab.
• To follow safety procedure in qc department.
• To analyze the Sample of in process validation and finish product on instrument such HPLC, GC,
UV, FTIR 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 online documentation.
• 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 Id2884381
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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