Founded in 1927 and headquartered in Warsaw, Indiana, USA, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopaedic 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 asap for a
Quality and Regulatory Affairs Specialist TEMP
Your main responsibilities:
Supporting the MDR (European Medical Device Regulation) project by supporting the EAR function of Zimmer GmbH by preparing the notifications of products to Swissmedic.
Support the Project Team in administrative tasks such as the collection of data and follow-up tasks as required in respect of EMEA QA Commercial and Distribution.
Support the Project Team in the role of Zimmer GmbH as a distributor of 3rd party products and support the implementation of respective actions.
Assist in preparing documents and procedures as required.
Your Qualifications and Experience:
Sound technical or administrative background (higher technical education preferred).
Broad knowledge of regulatory requirements (ISO 13485) and Quality processes.
Fluent in German and English and good report, business correspondence writing skills in English.
Good computer skills, including Microsoft Office, Excel, PowerPoint, Visio, SAP and SharePoint.
Autonomous, organized, rigorous and methodical operating.
Effective communication skills.
If you seize this opportunity, you will 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.