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• Identify, develop, and secure new business opportunities to achieve sales targets and expand market share in the assigned territory. • Build and maintain strong, long-term relationships with existing and prospective…
Prepare, review, compile, and submit regulatory dossiers for pharmaceutical products, including LVPs, sterile injectables, for domestic and export ROW markets. Handle regulatory submissions through CDSCO, State DCA,…
1. Responsible for implementation of cGMP in the plant. 2. Responsible for review of SOPs. 3. Responsible for preparation of Quality Documents such as SMF, Quality Policy etc. 4. Responsible for review and compilation…