- Extensive Exposure and Experience in oral solids, liquids, and injectables. Also both domestic as well as major export markets
- Responsible for cGMP & GLP Compliance & Quality Management System as per US-cGMP, EU-GMP, D&C Act.
- Responsible for Validation Programme & other regulatory documentation
- Must have Exposure to US / EU regulatory audits.
Qualification: B.Sc/B.Pharma, MS/M.Sc/M.Pharma
Experience: 10-15 Yrs
Ms. Payal Kapoor