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. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards.  We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.

What You Can Expect

The QARA Assistant, as part of the EMEA Quality Commercial & Distribution Team within the Commercial Organization, will be responsible for supporting the Quality Assurance & Regulatory Affairs function of the assigned region.

How You'll Create Impact Ensure compliance with the requirements of ISO 13485 Quality Management System, appropriate company policies and any other ISO if applicable or required in country (i.e. ISO9001, ISO14001, ISO37001 etc.).Ensure that local organization comply with industry specifications, standards and European as also in country regulations (i.e. European Medical Device Regulation (EU) 2017/745).What Makes You Stand Out

Quality Management System (QMS) Assistance.

Support EMEA teams on uploading EMEA SOPs.

Support EMEA teams managing / uploading local SOPs.

Initiating the ECN for EMEA documents.

Follow-up with Local teams on translations.

Support HR in creating and maintaining the EMEA curricula.

Support HR in assigning curricula to the right employee

Support EMEA colleagues for training completion

Provide support the EMEA organization in projects

Support the Quality Assurance and Regulatory Affairs function within EMEA Zimmer Biomet organization.

Assist with the maintenance, continuance, and improvement of the local Quality Management System (QMS) according to ISO 13485, European Medical Device Regulation (EU) 2017/745, any applicable local laws and corporate guidelines/policies.

Your Background General Secondary Education.English language is a basic requirement, high standard of English speaking-writing skillsFurther Education / Qualifications desirable, though not essential.Experience in working with / within Quality Management Systems.Experience with Windows Office Software, especially Excel and Power Point, and various databases SAP.

EOE/M/F/Vet/Disability