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Part-time Regulatory & Quality Writer - Medical Devices - (40-50%)

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-operative complications in implants ( 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 pre-operative 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 9 people in the heart of Zurich. You will be a significant part a purpose oriented group, a principal gear in team working as a whole and your daily output a structural pillar for the company overall success.  

Job description

You will be responsible for assisting the team with regulatory documentations as necessary to market Hylomorph products in EU and US. This position requires a very good understanding of medical ...

Read the full job description on Startup Jobs by investiere

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Full-time Product Engineer (Medical Devices) - Intern at Hylomorph in Zurich 12-10-2021

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Published at 21-09-2021
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