Founded in 1927 and headquartered in Warsaw, Indiana, USA, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopedic reconstructive products; sports medicine, biologics, extremities and trauma products; spine, bone healing, craniomaxillofacial and thoracic products; dental implants; and related surgical products.
We collaborate with healthcare professionals around the globe to advance the pace of innovation. Our products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Together with healthcare professionals, we help millions of people live better lives.
For the European Headquarters, based in Winterthur (Switzerland), we are looking for a
Job Summary
In this multifaceted position (Project one Year or longer) you will be responsible for the management of timelines, supporting the implementation of EU Medical Device Regulation (MDR) to assure compliance with its requirements.
Up to 5%.
If you seize this opportunity, you will be able to develop your international experience and be a part of a great and truly global team. Zimmer Biomet offers a wide range of challenging career advancement opportunities and a dynamic work environment. We look forward to receiving your complete application online.
Zimmer GmbH
Martin Th. Feusi
Human Resources Senior Generalist
Sulzerallee 8
8404 Winterthur
058 854 81 66
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