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We are an innovative medical device start-up focused on cardiac surgery, developing a novel vein harvesting system to improve outcomes in coronary artery bypass grafting procedures. Having successfully completed proof-of-concepts, we are now in the critical phase of finalizing our product design, preparing for certification, and transferring the design to manufacturing. Located in the west of Vienna with excellent access to public transport via the U4 line, we offer a dynamic and collaborative work environment where cutting-edge technology and life-saving solutions come together. Join us in shaping the future of cardiac surgery and making a real impact on patients’ lives.
As the Regulatory Affairs Manager, you will be the key driver of our regulatory strategy, ensuring our vein harvesting system meets all global regulatory requirements for CE marking, FDA clearance, and other certifications. You will lead the preparation and submission of regulatory documentation and work closely with authorities and notified bodies to bring our product to market. Your role will ensure that the development and commercialization processes comply with the necessary medical device regulations globally.
How to Apply
If you are excited by the challenge of regulatory affairs and want to help shape the future of cardiac surgery with a breakthrough technology, we would love to hear from you! Please send your CV and a cover letter to office@valeriot.com.
We have set a minimum gross salary of EUR4,000 per month for this position. However, we are open to offering higher compensation based on your qualifications and experience.
Valeriot FlexCo
Dipl.-Ing. Dipl.-Ing. Michael Flatscher
office@valeriot.com
Elßlergasse 26/8
1130 Wien
Web: http://www.valeriot.com
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