Medical Writer

Job description

Are you passionate about medical writing and ensuring regulatory compliance in the medical device industry? Do you want to play a key role in creating clinical documentation that supports patient safety and innovation? As part of our Clinical Affairs team, you will contribute to the development and maintenance of clinical evaluations and Post‑Market Clinical Follow‑up (PMCF) documentation for our hearing solutions portfolio. You will work closely with internal stakeholders and external authorities to ensure compliance with EU MDR and other regulatory requirements. As a Medical Writer, you’ll combine scientific expertise with regulatory knowledge – delivering high‑quality clinical documentation and acting as a trusted advisor within the organization. Working with us, you will receive: What tasks are waiting for you? - full‑time work agreement in an international organization - possibilities for learning and development opportunities, adapted to your needs and supporting your growth - hybrid work model, combining remote work opportunities with work in an office in the City Center - flexible working hours - benefits package including social benefits (private medical health care, insur...