Shape and strengthen Quality Management Systems while leading and developing a team of Quality System specialists
Job Summary
Shape and strengthen Quality Management Systems while leading and developing a team of Quality System specialists.
Ensure products and processes meet the highest regulatory and quality standards with patient safety at the center.
This position offers the opportunity to combine people leadership, strategic influence, and hands-on quality expertise in a global, regulated medical device environment.
Matching Summary
Shape and strengthen Quality Management Systems while leading and developing a team of Quality System specialists.
Skills & Requirements
Must-have
Quality Management Systems
ISO 13485, FDA QSR, EU MDR
Lead Quality System Specialists
Cross-functional collaboration
CAPA ownership and RCA
Nice-to-have
Pragmatic, solution-oriented mindset
Developing people and teams
Influencing in a matrix organization
High ethical standards and ownership
Key Requirements
Master's degree in science, engineering, or technical discipline
3-5 years medical device quality systems experience
Strong knowledge of ISO 13485, FDA 21 CFR Part 820, EU MDD/MDR, MDSAP