Senior Medical Writer (m/f/d)

Jotec GmbH Jobportal
Hechingen

Kaufmännische Berufe (Sonstige)
Publiziert: 07.10.2025

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

Senior Medical Writer (m/f/d) – Hechingen, Germany or Remote within EMEA

Your Strength

At least 4 years of experience in medical writing or a related field
Advanced degree in a scientific or technical discipline (PhD or MD preferred)
Solid clinical knowledge, ideally with background in Cardiology
Proven experience in authoring clinical research documents and regulatory submissions
Strong ability to independently evaluate and interpret medical literature and data
In-depth knowledge of medical writing standards, clinical evaluation (e.g. CERs, PMCF), and MDR requirements
Excellent English communication skills; scientific writing fluency is essential
Skilled in cross-functional collaboration with departments such as Clinical Affairs, R&D, RA/QA, and Marketing
Experience mentoring or reviewing work of junior medical writers is a plus

Your Contribution

Act as lead writer on complex projects (global/multi-project/new product development)
Write, review, and submit scientific manuscripts, abstracts, presentations, and regulatory documentation
Author Clinical Evaluation Reports (CERs), PMCF Plans, Clinical Evaluation Plans, and related documents
Independently conduct gap analysis and evidence assessments
Evaluate technical file documents (e.g. risk management, IFU) against clinical and literature data
Collaborate with internal stakeholders (Clinical, R&D, RA, QA, Marketing) and external partners (CROs, surgeons)
Support response to regulatory authority questions and submissions
Conduct state-of-the-art evaluations and risk/benefit assessments across the product lifecycle
Develop and implement literature search strategies and critically assess scientific validity and relevance
Take ownership of assignments with minimal supervision and contribute as a subject matter expert