Regulatory Affairs Specialist

About This Role

This Regulatory Affairs Specialist role involves securing regulatory approvals for innovative medical devices in the Indian market. The position offers an opportunity to work at the intersection of medical technology, regulatory compliance, and product innovation. You will collaborate with regional and global regulatory teams to support product registrations, submissions, and documentation. The role suits a regulatory professional seeking to deepen their expertise in a dynamic, internationally connected healthcare technology environment.

Responsibilities

• Collaborate with regional and global regulatory teams to support product registrations, submissions, and regulatory documentation
• Interpret local regulatory requirements and assess their impact on product development and commercialization
• Contribute to maintaining compliance with applicable Indian medical device regulations and import/export requirements
• Work closely with cross-functional stakeholders to help ensure that regulatory processes are accurate, efficient, and aligned with business objectives

Application Process

• Your application will be reviewed quickly, objectively, and fairly against the role's core requirements using an AI-powered matching process
• A shortlist of top-fitting candidates will be shared directly with the hiring company
• The final decision and next steps (interviews, assessments) are managed by the hiring company's internal team