Regulatory Affairs Manager (m/f/d)

Your Mission

• You support the “Imaging” product line throughout its entire lifecycle
• Coordinating and creating technical documentation for the assigned medical device groups is part of your responsibilities
• You identify global regulatory requirements for the assigned medical device groups
• Developing testing and approval strategies for global distribution is one of your tasks
• You continuously analyze and optimize processes
• Monitoring regulatory compliance throughout the entire product lifecycle is part of your role
• You work closely with development teams from other departments and ensure that they receive targeted training on regulatory requirements

Your Talents

• Completed scientific or technical studies
• Several years of professional experience in the field of regulatory affairs for active medical devices
• Knowledge of the relevant product standards
• Expertise in the field of medical devices, especially in the area of endoscopy/imaging and electrical safety desirable
• Confident manner in international project structures
• Strong communication skills and independent working style
• Very good knowledge of German and English

Your Benefits

• Flexible working hours & mobile working: In many areas, working hours and location can be arranged as required​
• 30 vacation days and various special payments​​
• Further training opportunities: Open in-house seminar program, extensive e-learning offering, professional development courses and much more
• Corporate benefits and bicycle leasing​
• Subsidy for private pension plan and company health management​
• Various childcare options – at the headquarters in Tuttlingen​
• Health, sports, cultural and leisure activities – offers vary depending on location​