Hiring for quality management systems and ISO 13485
August 17, 2021
Why do MedTech and medical device startups need ISO 13485 certified quality management systems? Now is an extremely exciting time to be a medical device
This new forum is a collection of stories from our team that talks about the changing landscape and
how companies and talents are positioning themselves.
Why do MedTech and medical device startups need ISO 13485 certified quality management systems? Now is an extremely exciting time to be a medical device
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Elena Kyria speaks to Regulatory Rapporteur about the current status of the medical devices job market…
Elena Kyria is an award winning talent acquisition specialist in the Medtech industry. She has worked with hundreds of professionals in Regulatory, Quality and Clinical roles in Europe, over the last 9 years. Elena is on the leadership team for RAPS (Regulatory Affairs Professionals Society) Swiss chapter, a member of the Healthcare Businesswomen’s association, career and professional branding coach, founder and moderator of the EU Medical Device Regulation Update Forum, and a speaker at industry events. In 2018, Elena was named one of the year’s top Millennial Shepreneurs by Insights Success Magazine.
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