Medical Writer (m/w/d)

## Your Contribution

• Draft, edit, proofread, and manage clinical documents such as CERs, CEPs, PMCF Plans & Reports, scientific articles and others
• Collaborate under supervision on moderately complex projects or support senior medical writers
• Coordinate document timelines and ensure timely delivery
• Conduct literature searches and appraisals in alignment with clinical and regulatory needs
• Assist in aligning documentation with risk/benefit assessments, current scientific literature, and regulatory standards
• Support meetings and communication related to clinical content and investigator materials
• Work closely with internal stakeholders (Clinical, R&D, RA/QA, Marketing) and external partners (surgeons, consultants, CROs)

## Our Strength

• A mission-driven, international work environment focused on innovation and quality
• Exciting projects with a global impact in the medical device industry
• Career development opportunities, including training programs and support for continuing education
• Flexible working models, including hybrid options
• Attractive benefits including pension schemes, EGYM Wellpass, and more

## Contact

Apply now and join the Artivion team. We are looking forward to receiving your application documents directly via our online system.

Brian Russo, T: +41 435

JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,

Lotzenäcker 23, 72379 Hechingen

[www.artivion.com](http://www.artivion.com/)

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Source: Statistisches Bundesamt (Destatis), table; dl-de/by-2-0; StarIn's calculation