Stryker Senior Director Regulatory Affairs and Quality Assurance (m/f) in Freiburg, United States
Your key responsibilities
As a Senior Director you are part of the Craniomaxillofacial (CMF) leadership team and responsible for the Regulatory Affairs and Quality Assurance department for our CMF division.
You provide leadership and direction for the development, implementation, and maintenance of the applicable regulatory and quality system requirements for all Craniomaxillofacial products and markets.
You are responsible for establishing a state of “audit readiness” and support successful regulatory audits.
In your role you collaborate strongly with R&D, marketing, sales and operations.
As a strong leader you will lead and develop an international team of talented manag-ers and RA/QA experts and focus on proactive succession planning.
What are we looking for?
You have a degree in business or related discipline.
You have at least 8 to 10 years of professional and leadership experience in a regulated industry working in Quality, Regulatory Affairs or similar.
You operate with confidence in international and complex surroundings.
You are characterized by a high level of communication skills, strategic thinking, analytical and negotiation skills as well as extensive interface competencies.
You have the willingness to travel domestically and internationally.
Your excellent English language skills enable you to collaborate with stakeholders on a global basis; German is preferable.
If you have any further questions please feel free to reach out to Kristina Boch via +49761 4888-766.
Work From Home: Yes
Travel Percentage: Up to 25%
Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. More information is available at www.stryker.com