Medical Writer (m/f/d)

Artivion EMEA; Hechingen; Hybrid; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading company in the medical device industry seeks a Medical Writer to produce high-quality clinical documents. Located in Hechingen or remote across Europe, the role demands collaboration with cross-functional teams and offers exciting projects with global impact. Join us for a mission-driven career with development opportunities and flexible working conditions.

Leistungen

Pension Schemes

Career Development Opportunities

Flexible Working Models

EGYM Wellpass

Qualifikationen

• 2–4 years of relevant professional experience in clinical or medical writing.
• Excellent command of written and spoken English.
• Experience with EU MDR and related clinical documents is a plus.

Aufgaben

• Draft, edit, and manage clinical documents including CERs and scientific articles.
• Collaborate on moderately complex projects and coordinate timelines.
• Conduct literature searches in line with clinical and regulatory needs.

Kenntnisse

Organizational Skills

Attention to Detail

Medical Writing

Data Analysis

Scientific Literature Research

Collaboration

Jobbeschreibung

• Hechingen
• Medizin, Pharmazie, Labor
• Publiziert: 21.05.2025
  
  

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: [phone]

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

Lotzenäcker 23, 72379 Hechingen

www.artivion.com