Regulatory Affairs Specialist - Zagreb, Croatia or Ljubljana, Slovenia
Must Haves
- Bachelor or Master degree iin a related field
- Proven track record of relevant regulatory and quality environment in medical devices
- Proven track record of experience working with complex databases
- General knowledge of GDP
- Proficiency in Croatian or Slovenian
- English language.
Nice to Haves
- Experience with device safety reporting
- Proficiency in Croatian or Slovenian
- Experience in Quality Systems
- Work experience working with distributors
- Work experience within large enterprises
Your Answer
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About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together.
