Regulatory Affairs Consultant - REMOTE India

Responsibilities:

• Handle new registrations, lifecycle management, and renewals of biologicals, vaccines, and other pharmaceutical products.
• Contribute to the preparation and delivery of regulatory submissions from a global and regional perspective.
• Prepare and review Marketing Authorization Applications & Variations for multiple regions.

Requirements:

• 6+ years of experience in regulatory affairs, specifically in pharmaceuticals and related products.
• Expertise in managing lifecycle and compliance for biologicals, vaccines, and small molecules.
• Strong knowledge of global pharmaceutical legislation and guidelines related to regulatory CMC aspects.

Benefits:

• Opportunity to work remotely and manage your own schedule.
• Collaborative team environment focused on health improvement.
• Access to continuous professional development and training.