At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world.

What You Can Expect

You will be responsible for supporting the Quality Assurance & Regulatory Affairs function of Portugal by:

• Ensuring compliance with the requirements of ISO 13485 Quality Management System, appropriate company policies and any other ISO if applicable or required in country (e.g. ISO9001, ISO14001, ISO37001 e.t.c).
• Ensuring local organization comply with industry specifications, standards and European as also in country regulations (e.g. European Medical Device Regulation (EU) 2017/745).

How You'll Create Impact

Qual...