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 talent 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 included, respected, empowered and recognised.
What You Can Expect
The Quality and Regulatory Affairs Associate is responsible of the product registration in different markets in accordance with the local legal requirements. You will also be the main contact between the organization and authorities to ensure reliable forward of information.
How You'll Create Impact
Top Level:
Support the implementation, maintenance, continuance, and control of a quality management system according to international standards and corporate guidelines/policies, where applicableAssure an effective, consistent, and reliable forward of information in terms of product surveillance in assigned region and local market in accordance with legal requirements and Zimmer Biomet procedures and as per instructions of the direct manager, where applicableEnsure the surveillance and forward of information concerning changes and/or new upcoming local legal requirements to assure the continuity of Zimmer Biomet’s business in assigned region
Detailed Tasks:
Support implementation, development, maintenance, and control of a quality management system according to international standards and corporate guidelines/policies/proceduresBe responsible for product registration on the market in accordance with local legal requirements; main contact for the local competent authority and responsibility for the maintenance of the business in the local marketAssure an effective, consistent and reliable forward of information in terms of product surveillance on the local market in accordance with legal requirements and Zimmer procedures Surveillance and forward of information concerning changes and/or new upcoming local legal requirements to assure the continuity of Zimmer Biomet’s business Support the internal and external audits; also within an internal auditor team coordinated by headquarters (if applicable)Be in continuous communication with QA/RA EMEASupport other Zimmer Biomet distribution organizations with regards to QA/RA requirements (e.g., product registrations)Get involved in special projects and special duties like (re-)validation of technical systems and proceduresWhat Makes You Stand Out
Experience with Windows Office Software, SAP eligibleEnglish language is a basic requirementSolid problem solving skillsAbility to work independently and under pressureOrganizational, follow up and time management skillsYour Background
B.S. degree in engineering, business, political science or equivalent experience0 to 3 years’ experience in registration activities and/or quality assurance
EOE/M/F/Vet/Disability