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Health Jobs
1 month
India
Rajasthan
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ID: 762094
Published 1 month ago by Cadila Pharmaceuticals Ltd
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In Health Jobs category
Udaipur, Rajasthan, India
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Ensuring Finish Section ,RM Section, PM Section, Equipment Qualifications, Validations (Analytical Method validation, Cleaning Method Validation Process Validation, Hold time studies and Stability study in QC lab, Udaipur
Principle task and Responsibilities:
• To ensure the compliance of Finnish Product/RM/PM in Quality Control Lab.
• To analyze the finished products, in process and samples by chemically / instrumental method.
• To receive the samples for analysis and making entry in Inward register.
• To maintain the Instruments log books related to FP analysis/RM analysis/PM analysis
• Over all responsibilities of FP/RM/PM/Validations section in absent of first and second line in charge.
• To plan the analysis and trouble shooting in absent of first and second line in charge.
• To analyze all validation samples and compilation of documents.
• To enter the finished product / raw material /Packing materials results through LIMS/Available resources.
• To analyze Market complaints samples.
• Follow cGMP in Laboratory.
• Any other activity assigned by QC head. Read more

Published on 2025/09/10. Modified on 2025/09/10.

Description

Ensuring Finish Section ,RM Section, PM Section, Equipment Qualifications, Validations (Analytical Method validation, Cleaning Method Validation Process Validation, Hold time studies and Stability study in QC lab, Udaipur
Principle task and Responsibilities:
• To ensure the compliance of Finnish Product/RM/PM in Quality Control Lab.
• To analyze the finished products, in process and samples by chemically / instrumental method.
• To receive the samples for analysis and making entry in Inward register.
• To maintain the Instruments log books related to FP analysis/RM analysis/PM analysis
• Over all responsibilities of FP/RM/PM/Validations section in absent of first and second line in charge.
• To plan the analysis and trouble shooting in absent of first and second line in charge.
• To analyze all validation samples and compilation of documents.
• To enter the finished product / raw material /Packing materials results through LIMS/Available resources.
• To analyze Market complaints samples.
• Follow cGMP in Laboratory.
• Any other activity assigned by QC head.
Cadila Pharmaceuticals Ltd
Cadila Pharmaceuticals Ltd
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