Must have broad understanding of the development of pharmaceutical products, regulatory and patent law globally. Patent and regulatory databases in different countries
Lead Commissioning, Qualification & Validation activities for equipment, utilities, and computerized systems. Develop & approve IQ, OQ, PQ, cleaning validation, process validation, and CPV documentation.
Perform accurate Book-in and data entry ICSRs into safety databases within defined timelines. Ensure compliance with regulatory guidelines, SOPs, and company quality standards for PV processes.
Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates.