Introduction

Join Us in Saving Lives - Become a Part of Artivion
At Artivion, we're driven by a powerful mission: to create high-quality, life-saving solutions for patients with aortic diseases. In close collaboration with surgeons across the globe, we deliver trusted technologies that make a real difference. Every team member plays a vital role in this mission -- including you. Bring your strengths, grow your expertise, and help shape the future of patient care.

We are hiring:
Medical Writer (m/f/d)
Location: Hechingen, Germany or Remote (Europe)
Full-time | Department: Clinical Affairs

Your Strenght

  • 2-4 years of relevant professional experience in clinical or medical writing.
  • Strong organizational skills and attention to detail.
  • Ability to interpret and explain scientific data from various sources including studies, literature, and technical documentation.
  • Excellent command of written and spoken English.
  • Proficiency in medical literature research, data analysis, and content development.
  • Experience collaborating with cross-functional teams such as Clinical, R&D, Quality, and Regulatory Affairs.
  • Experience with EU MDR (Medical Device Regulation), including familiarity with Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), Post-Market Clinical Follow-up (PMCF) plans, and other clinical evidence documents is an advantage.

Your Contribution

  • Draft, edit, proofread, and manage clinical documents such as CERs, CEPs, PMCF Plans, 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

Ready to Make an Impact?
We look forward to receiving your application documents in English. Apply now and become part of the Artivion team!
Contact: Brian Russo
+41 435 08 39 01
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.
Lotzenäcker 23, 72379 Hechingen
www.artivion.com
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