Medical Writer (m/f/d)

Artivion EMEA; Hechingen; Hybrid; EUR 55.000 - 85.000; Vollzeit

Benefits dieser Stelle

Flexible hybrid work

Pension scheme

EGYM Wellpass

Zusammenfassung

Artivion is seeking a Medical Writer (m/f/d) for Hechingen, Germany or remote across Europe. The role focuses on drafting and managing CERs, CEPs, PMCF plans, and other regulatory documents while coordinating with Clinical, R&D, QA/RA, and Marketing teams.

Ideal candidates have 2–4 years in clinical/medical writing, strong English, and excellent literature research skills. EU MDR experience is a plus, with a hybrid work model and international collaboration opportunities.

Qualifikationen

• 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 (including CERs, CEPs, PMCF plans, and other clinical evidence documents) is an advantage.

Aufgaben

• 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).

Kenntnisse

Medical writing

Regulatory awareness

Literature research

English proficiency

Cross-functional teamwork

EU MDR familiarity

Jobbeschreibung

• Hechingen
• Kaufmännische Berufe (Sonstige)
• Publiziert: 24.09.2026

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

Brian Russo, T: [phone]

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

Lotzenäcker 23, 72379 Hechingen

www.artivion.com