Join the client as a highly visible leader with full ownership of the Quality & Regulatory Affairs function, including team development and performance. This role provides end-to-end leadership across quality and regulatory activities, ensuring clear direction, strong execution, and continuous improvement to support business success and patient impact.
Responsibilities include defining and executing regulatory strategies across the product lifecycle, ensuring compliance with applicable regulatory requirements and quality standards (e.g., EU MDR and ISO 13485), and overseeing and continuously improving the Quality Management System (QMS). You will manage regulatory submissions and approvals, and coordinate interactions with relevant authorities and notified bodies as needed.
The client is seeking proven leadership experience in Quality and/or Regulatory Affairs within a highly regulated industry, ideally MedTech, along with deep expertise in relevant regulations and quality standards. The ideal candidate has a strong track record of building, leading, and developing high-performing teams, a strategic mindset with hands-on execution capabilities, and excellent stakeholder management skills in an international, matrix environment. A degree in a relevant field such as Life Sciences or Engineering is expected.