At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all
Job Summary
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all.
Ensure that product development projects and changes to existing products are conducted in compliance with FDA Quality System Regulations, EU MDR and inhouse Standards.
Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values.
Matching Summary
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all.
Skills & Requirements
Must-have
product design documentation review
risk management file development
ISO 14971
EU MDR hands-on experience
process validation requirements
verification and validation plans
Nice-to-have
statistical software tools
cross-functional team environment
DMAIC or DMADV(DFSS) methodologies
training development
audit participation
Key Requirements
5-8 years quality engineering experience
8-10 years overall experience
B.E or B.Tech in Mechanical Engineering
Familiar with statistical software tools
Familiar with ISO 13485, ISO 14971, IEC 60601
Hands-on experience on EU MDR
Working knowledge of FDA Quality System Regulation