Job Detail

Temp Senior Development Engineer (until December 2021) 100%

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Requisition Number

EMEA06367

Employment Type

Full-time

Location

Winterthur

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 Headquarter, based in Winterthur (Switzerland), we are looking for a

Temp Senior Development Engineer (until December 2021) 100%

In this position you will be responsible for the implementation of MDR (Medical Device Regulation) in Design Control and Risk Management for the existing orthopedic instruments and implants. You will work in a cross functional environment with Development teams such as Research, Quality Engineering, Regulatory Affairs, Supplier Quality and Operations ensuring all MDR aspects are captured in the Design Control and Risk Management files of all devices.

Your main responsibilities:

• Identifying and closing gaps to meet European MDR requirements as related to Design Control and Risk Management


• Initiating, managing and completing Technical Files, DHFs and change projects for design control and risk management documentation update


• Being involved in creating Design Control & Risk Management procedural adjustments to comply with MDR


• Interacting with research, quality engineering, labelling, sourcing and supplier quality departments in their design control and risk management related work


• Educating internal colleagues across departments and divisions

Your Qualifications and Experience:

• BSc degree in Mechanical or Biomechanical Engineering, or related discipline


• Minimum of 3-5 years of experience with Medical Device Product Development; preferably in orthopedic medical device industry with related regulatory requirements (MDD/MDR, international standards)


• Familiar with ISO 13485, quality management for medical devices as well as ISO 14971


• Knowledge of medical device product function & design (SAP)


• Demonstrating strong written and verbal communication skills, being comfortable to make presentations to internal audiences


• Fluent in German (written and spoken); working knowledge of English is a must

Travel Requirements:

This dynamic job position requires a willingness to travel (up to 5%).

 

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 online.

 

Zimmer GmbH
Angela Galliker
Sulzerallee 8
8404 Winterthur

www.zimmerbiomet.com

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