Head of regulatory affairs Medical devices
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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:
Your profil:
University degree in life sciences, biomedical engineering, or a related field. At least 10 years experience in regulatory affairs, preferably in the medical devices sector. In-depth knowledge of local and international regulations related to medical devices, such as FDA, EMA, and European directives. Proven experience in team management and leadership. Excellent communication skills and demonstrated ability to work collaboratively with multifunctional teams. Ability to work independently, manage priorities, and meet tight deadlines. Proficiency in English and German, both spoken and written; proficiency in french would be an advantage.