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EU MDR is a new EU regulation which requires all Medical Device’s to comply as per the required timelines. Supplier Quality Lead role lies within the Supplier Workstream to support implementation activities Divisionally. The following activities are responsibilities within the role

• Remotely Lead indirect Quality Engineer reports based Globally

• Report to the Program Manager escalations, risks and project status

• Execute Global Project activities

• Liaise with Sourcing partners

• Support all activities required by Divisions to support the execution of EU MDR Program

Work From Home: Occasional

Travel Percentage: 20%

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. More information is available at www.stryker.com