Medical Writer

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 Strength3–4 years of relevant professional experience in medical writing or regulatory for medical devices.Advanced degree in a scientific or technical discipline (PhD or MD preferred)Solid clinical knowledge, ideally with background in the Cardiovascular areaStrong organizational skills and attention to detailAbility to interpret and explain scientific data from various sources including studies, literature, and technical documentationExcellent command of written and spoken EnglishProficiency in medical literature research, data analysis, and content developmentExperience collaborating with cross-functional teams such as Clinical, R&D, Quality, and Regulatory AffairsExperience with EU MDR (Medical Device Regulation), including experience with Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), Post-Market Clinical Follow-up (PMCF) plans/reports, and other clinical evidence documents is an advantage Your ContributionDraft, edit, proofread, and manage clinical documents such as CERs, CEPs, PMCF Plans & Reports, scientific articles and othersCollaborate under supervision on moderately complex projects or support senior medical writersCoordinate document timelines and ensure timely deliveryConduct literature searches and appraisals in alignment with clinical and regulatory needsAssist in aligning documentation with risk/benefit assessments, current scientific literature, and regulatory standardsSupport meetings and communication related to clinical content and investigator materialsWork closely with internal stakeholders (Clinical, R&D, RA/QA, Marketing) and external partners (surgeons, consultants, CROs) Our StrengthA mission-driven, international work environment focused on innovation and qualityExciting projects with a global impact in the medical device industryCareer development opportunities, including training programs and support for continuing educationFlexible working models, including hybrid optionsAttractive benefits including pension schemes, EGYM Wellpass, and more ContactApply 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.,Lotzenäcker 23, 72379 Hechingenwww.artivion.com