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Job Description : |
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| 1. |
Ensuring 100% cGMP compliance in all the processes of manufacturing |
| 2. |
Overlooking batch release and its documentation |
| 3. |
Involvement in market complaint and ensuring implementation of corrective and preventive actions at the shop floor |
| 4. |
Ensuring validations related to sterility assurance |
| 5. |
Reviewing proper facility qualification and equipment qualification |
| 6. |
Responsible for preparation of master validation plan |
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| Qualification : B.Pharm / M.Sc. (Bio-Chemistry, Chemistry, Microbiology)
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| Experience : 9 - 10Yrs.
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| Desired profile : Candidate should have exposure of QA function of a pharma industry. Candidates having injectable exposure will be given preference. Exposure of regulatory plant is a must.
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| Location : Plant near Ahmedabad
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