Key Responsibilities:

• Further development and optimisation of existing products and technologies

• Analysis of customers and market requirements, technical clarification with customers and suppliers

• Development of new products and technologies up to series production

• Planning of project structures and organizations with internal and external partners

• Applying for and maintaining appropriate patent protection, competition and patent monitoring

• Approvals of new products with a focus on CE, FDA

• Preparation, monitoring and adherence to budget plans

• Efficient planning, coordination and management of the development project portfolio

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Key Requirements:

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• You are a visionary, assertive and at the same time down-to-earth leader with a degree in Mechanical Engineering, Biomedical Engineering or related field - Ph D a plus

• At least 15 years of professional and management experience in research and development work in the field of medical technology

• 10 years of experience in Management building and leading teams

• Leadership skills, ability to work in a team and in-depth knowledge of modern project management methods including development tools

• Knowledge of regulatory requirements (MDR, FDA, NMPA, DIN EN ISO 13485, DIN EN ISO 14971)

• A high degree of initiative and motivation

• Analytical way of thinking, independent and decisive way of working

• A friendly, confident and consistent manner in communication with the necessary tact

• Very good written and spoken French and English skills