Head Regulatory Affairs / Medtech (m/f/d)

Tasks / Main Responsibilities:

• Lead and support the registration and approval processes for all medical devices outside the EU.
• Collaborate effectively with distribution partners, service providers, and regulatory authorities.
• Assess international approval requirements, and prepare and review regulatory documentation with internal specialists.
• Manage regulatory projects, ensuring timely adherence to deadlines and schedules.

Qualifications / Personality:

• University degree and initial professional experience in the field of international medical device approvals
• Good understanding of technology and complex interrelationships
• Interest in working with international legal requirements and regulations
• Good problem-solving and communication skills
• Intercultural competence and very good command of spoken and written English

Benefits:

• Flexible working hours
• Induction programme and on-demand training
• Family-friendly work environment
• Occupational health and safety management
• Occupational pension plan
• Secure job in a modern company