It’s a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together.
We are hiring a Medical Writer (m/f/d) Location: Hechingen, Germany or Remote (Europe)
Your Strength
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
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 08 39 01
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,