In Process QA for a WHO/GMP Approved Pharma unit

    • Haridwar, Haridwar, Uttarakhand, India
Job Description

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

Job Description:

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.
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