You are specialist and disciplinary manager of the Regulatory and Clinical Affairs department of one or more product lines in the respective division (BS)

You are overseeing a team with an emphasis on talent development.

You are responsible for driving the Regulatory Affairs Development and Strategy.

You have the overarching responsibility, approving and obtaining approval for product of the product line, implementing for the Regulatory Affairs Lifecycle or Clinical Affairs (Clinical Evaluation and Strategy)

You are supporting the further development of the department, effectively enhancing expertise by introducing innovative concepts for the design and implementation of (global) clinical trials.

You are fostering collaboration with interface departments and guarantee increased value to our specialty department.

Completed natural science or technical studies with bachelor or master's degree (or corresponding professional experience)

Significant professional background, which includes experience in regulatory/clinical fields.

Relevant expertise in the international product registration of Class I to Class III medical devices

Proven leadership and team management skills within international, inter-cultural and diverse environments.

Solid business understanding and entrepreneurial approach

Interaction with regulatory bodies and outside representatives

Stakeholder management of different disciplines and hierarchy levels

Understanding Regulatory Compliance

Understanding processes, digitalization in medical technology and operational excellence

Exceptional English and fluent German communication skills, both spoken