Sr QC Manager
Sr QC Manager
Posted on :
02-01-2025
Employer Active
1 Vacancy
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Job Description
Job description:
To approve or reject as sees fit starting materials packing materials intermediate bulk and finished product.
Checking & approval of finished product reports.
Preparation & approval of standard operating procedures in quality control (chemical section).
Preparation & approval of specifications & method of analysis for raw materials bulk & finish products.
Documentation of finished products.
Documentation & maintenance of samples for stability study.
Overall documentation of quality control (chemical section)
Communication to a public testing lab.
Stability sample sending to public lab
Preparation of analytical chemist validation and maintaining the records for the same.
To ensure that all necessary testing is carried out and the associated records evaluated.
To approve specifications sampling instruction test methods and other Quality Control Procedures
To approve and monitor any contract analysts.
To ensure the qualification and maintenance of the department premises and equipment.
Preparation of excel sheet validation.
Checking of all instrument calibration records and prepared the calibration schedule.
To ensure that the appropriate validations are done.
To ensure that all necessary testing is carried out and the associated records evaluated.
To approve specifications sampling instruction test methods and other Quality Control Procedures
To ensure that the required initial and continuing training of his department personnel is carried out and adapted according to need.
Checking of all instrument calibration records and preparation of calibration schedule.
Daily job allocation Pharma Background Only
To approve or reject as sees fit starting materials packing materials intermediate bulk and finished product.
Checking & approval of finished product reports.
Preparation & approval of standard operating procedures in quality control (chemical section).
Preparation & approval of specifications & method of analysis for raw materials bulk & finish products.
Documentation of finished products.
Documentation & maintenance of samples for stability study.
Overall documentation of quality control (chemical section)
Communication to a public testing lab.
Stability sample sending to public lab
Preparation of analytical chemist validation and maintaining the records for the same.
To ensure that all necessary testing is carried out and the associated records evaluated.
To approve specifications sampling instruction test methods and other Quality Control Procedures
To approve and monitor any contract analysts.
To ensure the qualification and maintenance of the department premises and equipment.
Preparation of excel sheet validation.
Checking of all instrument calibration records and prepared the calibration schedule.
To ensure that the appropriate validations are done.
To ensure that all necessary testing is carried out and the associated records evaluated.
To approve specifications sampling instruction test methods and other Quality Control Procedures
To ensure that the required initial and continuing training of his department personnel is carried out and adapted according to need.
Checking of all instrument calibration records and preparation of calibration schedule.
Daily job allocation Pharma Background Only
Employment Type
Full Time
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