I applied online. I interviewed at Medtronic (Los Angeles, CA)
Interview
Responsibilities may include the following and other duties may be assigned. Directs or performs coordination and preparation of document packages for EU MDR regulatory submissions from all areas of company. Leads or compiles all materials required in submissions. Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. Monitors and improves tracking / control systems. Keeps abreast of regulatory procedures and changes. May direct interaction with regulatory agencies on defined matters. Recommends strategies for earliest possible approvals of clinical trials applications.
I applied through college or university. The process took 2 days. I interviewed at Medtronic (Hyderābād) in Nov 2025
Interview
1st exam they kept an assessment to check the standards of the students and then an interview. the interview was difficult and about the laws and in details about the indian laws, also about the basic C language, aptitude
I applied through other source. I interviewed at Medtronic (Maribor) in Jan 2025
Interview
4 rounds of interviews. first round recruiter and second was technical more excessive part, Third one with HR with all personality question, really detailed, Last one with general manager type of strategic thinking and really pleasant interview.
Interview questions [1]
Question 1
Usual questions about my current work, experiences, examples of work in stress situations etc
Very friendly and systematic. Interview process was systematic and well organized. One of the most comfortable interviews. It was not lengthy. They were friendly and co-operative, they were three rounds and co-operative when it came to deciding the interview slots.