Opening for Laboratory Quality Assurance @ Zydus Cadila
Job Description
Experience: 3 to 5 yrs
Qualification: M.Pharma
To prepare / review Chemical and Microbiological analytical method validation, Transfer and Verification protocol and report.
To review RM/PM specification, in-process specification, finished product specification, shelf life specification and its relevant MOA.
To review Testing work sheet of RM/PM, In-process, finished product, shelf life and its relevant reports.
To review SOPs of quality control department.
To perform routine checks in quality control department for assurance of cGMP in the Quality Control Department.
To ensure the compliance of current Good Manufacturing Practices in the Quality Control Department.
Handling, storage and withdrawal of stability samples.
To review stability results summary.
To prepare standard operating procedures at regular intervals to meet regulatory requirements.
To prepare / review stability study protocol/other study protocol and its reports.
To raise Change control, Deviation control, Incident, Corrective & Preventive Action.
Issuance, Retrieval, destruction of SOP, protocol, specification, method of analysis, job responsibilities and other documents.
Any other responsibility assigned by the Department Head.
Click here to apply directly
Job Description
Experience: 3 to 5 yrs
Qualification: M.Pharma
To prepare / review Chemical and Microbiological analytical method validation, Transfer and Verification protocol and report.
To review RM/PM specification, in-process specification, finished product specification, shelf life specification and its relevant MOA.
To review Testing work sheet of RM/PM, In-process, finished product, shelf life and its relevant reports.
To review SOPs of quality control department.
To perform routine checks in quality control department for assurance of cGMP in the Quality Control Department.
To ensure the compliance of current Good Manufacturing Practices in the Quality Control Department.
Handling, storage and withdrawal of stability samples.
To review stability results summary.
To prepare standard operating procedures at regular intervals to meet regulatory requirements.
To prepare / review stability study protocol/other study protocol and its reports.
To raise Change control, Deviation control, Incident, Corrective & Preventive Action.
Issuance, Retrieval, destruction of SOP, protocol, specification, method of analysis, job responsibilities and other documents.
Any other responsibility assigned by the Department Head.
Click here to apply directly
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