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1) Responsible for regulatory affairs.
2) Responsible for organizing product licenses
3) Responsible for authorization of production, BMRs and document review
4) Responsible for Marketing Authorization
5) Responsible for supervising QMS.
6) Ensures GMP is adhered.
7) Ensure customer complaints are resolved.
8) Liaison with Government and Statutory Agencies and Medical Institutions
9) Conduct training for pharmacists on QMS, CGMP and Job related aspects.
10) Attend to any incidental work that may be required by the factory manager.
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