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