Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.
In 2020, Eurofins generated 5.4 billion Euro proforma turnover in 800 laboratories across 50 countries, employing about 50.000 staff.
Position Summary: We are seeking a Document Writer (Scientific Documentation & Technical Communication) to support scientific writing outputs through coordination, technical oversight, and document lifecycle management. This role sits at the intersection of science, communication, and project management, ensuring that scientific documentation is complete, consistent, timely, and publication‑ or audit‑ready.
While this role is not primarily responsible for authoring scientific content, it serves as a key coordinator of scientific documentation by managing reviews, integrating subject matter expert input, and ensuring document readiness within a regulated environment.
Key Responsibilities
Scientific Document Coordination
Technical Communication & Quality Oversight
Project & Timeline Management
Cross‑Functional Collaboration
Role Context in Large or Regulated Organizations
In alignment with best practices in CROs and regulated laboratories, this role functions within a segmented documentation model, where:
This position plays a key role in the document coordination layer, while contributing directly to high‑quality scientific writing outputs.
Qualifications
Preferred Qualifications (M.Sc / M. Pharm with 5-7 years of experience)
- Scientific or technical discipline (e.g. CCIT/Package Testing preferred, Chemistry, Biology, Life Sciences, Engineering)
-Experience coordinating technical or scientific documentation
-Familiarity with regulated environments (GMP, GxP, clinical research, or equivalent)
-Strong written communication skills with attention to detail and consistency
-Demonstrated ability to manage multiple deliverables and competing priorities
Typical Backgrounds for This Role: Candidates may come from roles such as:
-Technical Project Manager
-Clinical Project Coordinator
-Scientific Program Manager
-Client Technical Liaison
Experience in CROs, GMP laboratories, clinical research, or regulated scientific environments is strongly preferred.
Abilities and/or Skills: