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 recognized.

 

What You Can Expect

 

As a Quality & Regulatory Affairs Specialist (m/w/d), you will be in charge of providing support to Capital Equipment servicing as well as to EMEA Quality and Regulatory Organisation to ensure quality and regulatory compliance.

How You Create Impact

 

Establish, implement and improve service processes, procedures and best practicesEnsure efficiency and accuracy of service department's administrative processes Coordinate and administrate scheduled maintenance activities, emergency repairs and equipment installationsParticipate in special projects and special duties like (re-)validation of technical systems and proceduresPlay a key role in growing revenue and margin from spare parts and service contractsParticipate and join strategic initiatives for the service department that align with overall business objectivesAdvise general management and work close together with other departments to support the businessWhat Makes You Stand Out

 

You have a proven track record in working within Capital Equipment servicing, ideally in Medical Devices or Pharmaceutical industry. 

You have developped the ability to work both independently as well as in a matrix organisation and to collaborate with stakeholders across all organisation. 

What Will Make You Successful

 

Knowledge of ISO 13485 and the Medical Device Regulation desirableAbility to prepare high quality, clear communication materials to the appropriate audienceAdvanced IT skills – Excel, PowerPoint, Windchill, SAPFluency in German and in EnglishDiscretion and confidentiality

EOE/M/F/Vet/Disability