Company Description

Eurofins Scientific through its subsidiaries is a world leader in food, environment, pharmaceutical and cosmetic product testing, discovery pharmacology, forensics, advanced material sciences, and in agroscience Contract Research services. It is also one of the global independent market leaders in genomics and in the support of clinical studies, as well as in BioPharma Contract Development and Manufacturing. In addition, Eurofins is one of the key emerging players in specialty esoteric and molecular clinical diagnostic testing in Europe and the USA. With ca. 62,000 staff across a network of over 1,000 independent companies in 62 countries and operating over 900 laboratories, Eurofins offers a portfolio of over 200,000 analytical methods for evaluating the safety, identity, composition, authenticity, origin and purity of biological substances and products, as well as for innovative clinical diagnostics. The objective of Eurofins companies is to provide their customers with high-quality services, accurate results on time and expert advice by their highly qualified staff.

Eurofins DiscoverX® is the trusted drug discovery and development product solutions provider. As the products division of Eurofins Discovery, and part of the Eurofins BioPharma global network, DiscoverX has earned this reputation over the past two decades by contributing to the discovery and development of life-saving therapeutics with trusted and validated cell-based assay products used in the screening and validation of billions of data points for countless therapeutic programs. The DiscoverX product portfolio is comprised of fit-for-purpose solutions, from ready-to-use homogeneous assay kits, stable engineered cell lines, membrane preps, recombinant proteins/enzymes, and qualified reagents to support your therapeutic drug programs no matter what stage you are at to accelerate your programs with confidence.

Job Description

Eurofins DiscoverX is seeking a detail-oriented Scientific Writer to conceptualize and author high-quality technical documentation for its product portfolio. The writer will be responsible for developing key scientific assets—including White Papers, Application Notes, and eBooks—to support the company’s diverse product lines. This role requires close collaboration with cross-functional teams to refine and finalize these technical materials.

Key Responsibilities

Product Documentation: Create and revise User Manuals for all products.Content Revision: Update existing manuals to align with current templates, stakeholder feedback, and updated product specifications.Technical Marketing Collateral: Write and edit high-level scientific content, including White Papers, Application Notes, and eBooks.Customer Support Assets: Develop FAQs, Quick Guides, Datasheets, and website landing page content to improve the user experience.Stakeholder Collaboration: Work closely with internal scientific teams to incorporate edits and ensure technical accuracy in all customer-facing materials.

Qualifications

 

Required Skills & Qualifications

Educational Background: Bachelor’s or Master’s in biotechnology, Molecular Biology, Biochemistry, or a related Life Sciences field.Technical Writing Experience: 2-5 years of experience in technical writing within the biotech or pharma industry.Scientific Literacy: Ability to understand and document complex laboratory procedures, specifically involving cell-based assays and protein engineering.Software Proficiency: Expert knowledge of MS Office Suite and experience with documentation version control. Proficiency in visual tools such as Bio Render or Adobe Illustrator is requiredCommunication: Exceptional command of the English language with the ability to simplify technical jargon for diverse global audiences.Ability to meet tight timelines and maintain flexible work hours for global team coordination.

Preferred Experience

Prior experience writing for a global pharma or life sciences product company.Familiarity with creating SEO-friendly content for blog posts and landing pages.Experience working with cross-functional teams across different time zones (US/Europe).

Interested candidates should submit their updated resume along with a portfolio or relevant writing samples (e.g., user manuals, white papers, or technical protocols) that demonstrate the applicant’s ability to communicate scientific and technical information clearly.