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Post: Back to all jobs In Process QA for a WHO/GMP Approved Pharma unit
No.of post: 12
- Preparation and Approval of Standard operating Procedures
- Preparation of Process validation Protocols and summary reports based on the Analytical results and Batch documents data.
- To co-ordinate the Qualification / Validation of the Equipment, Systems and Process.
- To ensure the issuance of required documents and samples for Drug and Regulatory Affairs.
- To ensure the preparation, Issuance, Revision/Review and Retrieval of the documents.
- To investigate the cause of any non conformance and its corrective / preventive action.
- To ensure the Analytical method validation of cleaning process before conducting Cleaning validation.
- Preparation of Cleaning Validation Master plan.
- Preparation and Execution of Cleaning validation protocols.
- Cleaning Validation Analytical Data collection and Summary report preparation cleaning validation.
- To conduct or organise revalidation activity at the defined frequency.
- To control the inventory of control samples.
Experience: 1 -5 yrs
Education: B.Pharma/M.Pharma,BSc/ M.Sc, any Science Background.
Industry Type: Pharma/ Biotech/Clinical Research.
Compensation: 2 - 3.5 lakhs/anum
Experience: 1-5 Years
Qualification: Any science stream
Industry Type: Pharma-WHO GMP
Functional Area: QA/qc
End Date: 4th October, 2016
You can send resume on PBSOLUTION3@GMAIL.COM
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