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Job Description
- Validation,Qualification & Calibration
- Technical Writing of Validation Documents (Risk Assessment, Validation Plan, Design Configuration/Specification, User Requirements, Functional Requirements, IQ OQ PQ, Trace Matrix, Validation Summary Report), SOPs, Maintenance Procedures, Calibration Procedures, and other instrument support documents.
- Follow up overall qualification/validation activities include( HVAC, thermal mapping, machine qualification, laboratory instrument qualification, etc….).
- Provide inputs to and administration of the site master validation program as well as assist in maintaining the site validation master plan.
- Develop validation policy with roles and responsibilities.
- Author, Review, Execute process validation protocols and validation summary reports.
- Perform validation testing and analyze data for validation documentation to determine acceptability.
Job Requirements
- BSC: Pharmacy or Science
- Gender: Male
- Experience: not less than 4 years’ experience in a similar position in
the pharmaceutical
