Head of regulatory affairs Medical devices

As the Head of Regulatory Affairs, you will be responsible for overseeing and leading the regulatory affairs team for a company specializing in medical devices. You will work closely with the research and development, quality, manufacturing, marketing, and sales departments to ensure regulatory compliance for all products and processes.

Responsibilities:

• Manage and lead the regulatory affairs team, including activity planning, goal setting, and performance evaluation.
• Develop and implement regulatory strategies to ensure compliance with local and international standards.
• Ensure timely and effective submission of regulatory filings to relevant authorities, including new product approvals, renewals, and modifications.
• Evaluate regulatory requirements for new products and changes to existing products, providing strategic guidance to the product development team.
• Manage interactions with regulatory agencies and external ...