Head of Quality and Regulatory Affairs (m/w/d)

• You will take on a highly visible leadership role with full ownership
• Join a dynamic, international company at the forefront of MedTech innovation

About Our Client

Our client is an international, innovation-driven MedTech company with a strong growth trajectory in Europe. The organization operates in a highly regulated environment, combining cutting‑edge technology with a clear focus on quality, compliance, and patient impact.

Job Description

• Full ownership and leadership of the Quality & Regulatory Affairs function, including team development and performance
• Definition and execution of regulatory strategies across the product lifecycle
• Ensuring compliance with all relevant regulatory requirements and quality standards (e.g., MDR, ISO 13485)
• Oversight and continuous improvement of the Quality Management System (QMS)
• Management of regulatory submissions, approvals, and interactions with authorities and notified bodiesActing as a key strategic partner to internal stakeholders across R&D, Medical, and Commercial functions

The Successful Applicant

• Proven leadership experience in Quality and/or Regulatory Affairs within a highly regulated industry, ideally MedTech
• Deep expertise in relevant regulations and quality standards (e.g., EU MDR, ISO 13485)
• Strong track record in building, leading, and developing high‑performing teams
• Strategic mindset combined with hands‑on execution capabilities
• Excellent stakeholder management skills and ability to operate in an international matrix environment
• Degree in Life Sciences, Engineering, or a related field

What's on Offer

• A high-impact leadership position with strong visibility and direct influence on business success
• An international, innovative MedTech environment with significant growth ambitions
• The opportunity to shape regulatory and quality strategy in a cutting‑edge technology setting
• A competitive compensation package along with long‑term career development opportunities