Admin Coordinator/Regulatory Assistant

About the Company

We are a growing medical device company committed to delivering high-quality healthcare solutions that meet international regulatory and quality standards. We are seeking a motivated and detail-oriented professional to join our Regulatory Affairs team.

Key Responsibilities

• Prepare, review, and maintain regulatory documentation for medical devices

• Handle product registrations, renewals, and regulatory submissions with local and international authorities

• Maintain technical files, product licenses, declarations, and compliance records

• Ensure products comply with applicable medical device regulations and standards

• Monitor updates and changes in regulatory requirements and communicate impacts internally

• Coordinate with manufacturers, suppliers, and internal departments to obtain required regulatory documentation

• Maintain document control systems and regulatory databases accurately

• Ensure smooth office operations and timely completion of assigned tasks

• Coordinate with internal teams and external vendors when required

How to Apply

Please email your CV to [synlifesolutionsv@gmail.com]

Whatsapp: 076 828 5054