The Quality Management Specialist will support the continuous improvement, compliance, monitoring, and harmonization of an integrated medical device Global Quality Management System
Job Summary
The Quality Management Specialist will support the continuous improvement, compliance, monitoring, and harmonization of an integrated medical device Global Quality Management System.
Key responsibilities include managing QA documentation, coordinating change requests, supporting investigations for critical quality topics, and participating in audits.
The role requires a minimum of 2 years of experience in a regulated industry, fluency in English, and knowledge of relevant quality standards and regulations.
Matching Summary
The Quality Management Specialist will support the continuous improvement, compliance, monitoring, and harmonization of an integrated medical device Global Quality Management System.
Skills & Requirements
Must-have
ISO 13485
FDA QSR
Document Control
Change Control
SAP DMS
Quality Management System
Nice-to-have
AI applications for process optimization
German or additional languages
Digitalization and automation initiatives
Key Requirements
Minimum 2 years of professional experience in regulated industry
Higher education (bachelor or master degree) or equivalent