The Quality Systems Specialist will handle the QMS, GMP and PMV operations to ensure the company is operating and meeting the established quality standard of medical devices across all business
Job Summary
The Quality Systems Specialist will handle the QMS, GMP and PMV operations to ensure the company is operating and meeting the established quality standard of medical devices across all business.
Responsibilities may include conducting internal audits, managing change control and risk management, handling product complaints, and executing field corrective actions.
Medtronic offers a competitive Salary and flexible Benefits Package, recognizing employee contributions and sharing in their success.
Matching Summary
The Quality Systems Specialist will handle the QMS, GMP and PMV operations to ensure the company is operating and meeting the established quality standard of medical devices across all business.
Skills & Requirements
Must-have
QMS, GMP and PMV operations
Korea QMS and ISO 13485
internal audit and CAPA
Post Market Surveillance audit support
change control and risk management
Product Complaint handling
Adverse Event Reporting
Nice-to-have
achievement oriented
drive results with highest quality
high attention to detail
excellent problem-solving skills
collaborate with global teams
Key Requirements
Bachelor’s degree in medical, biological science or equivalent