Preparation of validation protocols and its reports.
Preparation of monthly reports
Ensuring that the production facilities are clean and hygienic.
Handling of Deviations followed by preparation of investigation reports by discussing with cross-functional team and closure for deviations in GMP Pro.
Initiation and closure of planned change, change controls, initiation of procedure and CAPA manufacturing of intermediates and API\xe2\x80\x99s.
Handling of Risk assessments and impact assessments for respective changes. Ensure that new appropriate, modified facilities and equipment are qualified.
Ensure the premises and equipment are maintained.
Ensure that all the production deviations are reported and evaluated, that critical deviations are investigated, and the conclusions are recorded.
Participating in cGMP, production, and safety-related training activities.
Train the concerned personnel as a department training coordinator.
Prepare and approve the (If required) protocols and reports.
Co-operate with the maintenance department in the execution of preventive maintenance schedules for production-related equipment and other Job orders.
Coordinate with all CFT departments.
Qualification B.Sc(chemistry)/M.Sc(organic Chemistry) Experience 04 to 08 Years
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