Technical Writer Medical Devices and Combination Products

Kurosbio

4 days ago

Bilthoven, Utrecht

Onsite

Full Time

Senior

0 applicants

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About this role

A Technical Writer – R&D Design Controls supports the full design and development lifecycle for high-risk medical devices and combination products, ensuring compliant and traceable documentation throughout the Design History File (DHF). The role requires collaboration with engineers, scientists, QA/RA, and clinical teams to maintain technically sound and regulatory compliant documentation.

Skills

Qualifications

MSc or Ph.D. in chemistry, (medical) biology, biomedical technology, or similar5 years of experience supporting medical device design and development documentationDirect experience with writing design related documentations (e.g., risk management, human factors, design V&V)

About Kurosbio

kurosbio.com

Kuros Biosciences is a medical biotechnology company that develops biologic bone graft technologies—most notably MagnetOs—designed to stimulate bone growth and prevent non-unions. The company focuses on targeted, controlled fusion technologies that combine innovation with strong clinical evidence to advance bone healing. Its products are intended to support surgeons in fusion and orthopedic procedures and improve patient outcomes. Kuros’s mission is to discover, develop and deliver solutions that eliminate non-unions and accelerate reliable bone repair.