A world-renowned Medical Technology firm is looking to expand their team and are actively looking to recruit a Director of Quality Assurance and Regulatory Affairs. The role offers you the opportunity to join a fast-paced and vibrant company which firmly believes in a methodical, detail-based approach to ensure the highest quality product possible.
The role:
Maintaining the Quality Management System in accordance with regulatory standards (ISO13485, 14971, EU MDR and FDA)
Leading a team of 15 Quality Associates, facilitating the expansion of the company and the development of personnel
Development of mechatronic systems to be approved by notified bodies
Helping the firm to remain at the cutting edge of the market by mapping market trends, innovating new techniques and participating in ongoing training to keep the team up to date with these factors.
Requirements:
Bachelor's degree in biomedical engineering or another relevant field
10+ years' experience in industry, additional experience managing a team
Extensive knowledge of ISO 14971 and ISO 13485
FDA, EU MDR and ISO literacy
French and English fluency required, spoken German preferred but NOT essential
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Benefits:
Facilitation of exponential career growth
Extensive bonus packages and incentives
The opportunity to work alongside an advanced and ever evolving team within the Class III Medical Devices field
Research and publication opportunities
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Location- Brussels
Employment type - Permanent, Hybrid working
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How to Apply:
To apply for this exciting opportunity, please register your interest by emailing your CV to Charlotte at
