Job Description
**J** **oin our EU MDR team** responsible for verifying medical documentation for compliance with European regulations. Our team is part of the Quality & Regulatory function, contributing to Patient Safety & Quality.
**Your role:**
+ Monitor and audit third-party orders containing medical devices.
+ Prepare and execute quality inspection activities on EU-MDR regulated medical devices, including analysis and submission of identified issues to the responsible team.
+ Create verification records in SAP and archive documents related to customers and countries in accordance with local legislation.
+ Provide proactive feedback to GBS management and external suppliers based on the experience gained.
+ Take initiative and actively participate in process improvements.
**You're the right fit if:**
+ You have 1+ years of relevant experience in a business operational environment, connected with healthcare, medical environments, quality, or audit.
+ You are fluent in Engl...
**Your role:**
+ Monitor and audit third-party orders containing medical devices.
+ Prepare and execute quality inspection activities on EU-MDR regulated medical devices, including analysis and submission of identified issues to the responsible team.
+ Create verification records in SAP and archive documents related to customers and countries in accordance with local legislation.
+ Provide proactive feedback to GBS management and external suppliers based on the experience gained.
+ Take initiative and actively participate in process improvements.
**You're the right fit if:**
+ You have 1+ years of relevant experience in a business operational environment, connected with healthcare, medical environments, quality, or audit.
+ You are fluent in Engl...
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