Part-time Regulatory & Quality Wizard - Medical Device - (Freelance)

at Hylomorph in Zurich CH

Who we are

HYLOMORPH is a pre-commercial clinical-stage MedTech company based in Zurich, Switzerland. In a dynamic startup environment, our team is developing a platform technology for implantable medical devices aimed at preventing post-surgical complications in implants (www.hylomorph-medical.com). Our pre-clinical study has proven excellent safety and tolerability of our devices, as well as a striking reduction of the inflammatory reaction and fibrotic encapsulation in pacemakers and breast implants. Our product consists in an easy-to-handle hydrogel pouch that tailor fits target implants and optimizes their interaction with the surrounding hosting tissue, finally re-establishing the health in the surgical pocket.

We closely collaborate with hospitals in Germany where our first-in-man clinical trial is currently ongoing, towards CE mark and FDA authorization.


We offer a stimulating and friendly entrepreneurial environment, with a team of 8 people in the heart of Zurich. You will experience all aspects of medical device life cycle management and startup development. 


Job description

We are seeking a reference independent Regulatory & Quality Affair Expert who shall provide ad-hoc support to our team in ALL required actions in the preparation of our technical files towards CE-mark and FDA authorizations as well as ensure compliance of our QMS. 

The primary responsibility of ...

Read the full job description on Startup Jobs by investiere



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Published at 22-06-2020
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