Laurus Bio is a subsidiary of Laurus Labs and is an integrated research-driven biomanufacturing organization with over 15 years of experience in precision fermentation and recombinant DNA technology.
You will be working closely with internal Product Management and external stakeholders to ensure Product Launches for our Life Science Business are on time. You must understand laws and regulations across the globe governing GHS, Safety data Sheets, Trade Compliance and Chemical Registration.
Provide accurate, timely, and value-added scientific responses to medical queries from healthcare professionals, patient groups, consumer groups, government authorities, and the field force.
The role holder is responsible for supervising and executing the manufacturing operations for Compression, Encapsulation, Coating, and Packing sections in a highly regulated pharmaceutical environment.
To manage and support European regulatory activities for medicinal products across the EU lifecycle, including new registrations, variations, renewals, and regulatory maintenance, while coordinating with EU CMOs, MAHs, and regulatory authorities to ensure full compliance with EU legislation.