Technical Writer

🔥 4 minutes ago

🌪️ Kansas – Remote

🌪️ Kansas – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔏 Technical Writer

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Eurofins

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1987

🔬 Science

🧬 Biotechnology

⚕️ Healthcare Insurance

💰 $30M Grant on 2021-10

Science • Biotechnology • Healthcare Insurance

Eurofins is a global leader in testing and laboratory services. With approximately 62,000 employees and over 900 laboratories across 62 countries, the company provides a wide range of testing services across various industries. Eurofins offers services such as food and feed testing, consumer product testing, genomic services, clinical diagnostics, forensic services, environment testing, and pharmaceutical testing. The company is committed to scientific innovation and sustainability, and it plays a critical role in testing for health, safety, and environmental impacts worldwide.

📋 Description

• Developing, reviewing, and maintaining controlled documentation that supports validation and laboratory operation activities • Ensuring that standard operating procedures (SOPs), forms, protocols, and other technical documents are accurate, clear, and compliant • Collaborating with cross-functional subject matter experts to manage documents, support quality initiatives, and promote consistency and continuous improvement • Writing and editing forms, protocols, reports, and procedures from existing templates under supervision • Analyzing documents to maintain continuity of style and content • Performing updates and revisions to technical documents as instructed • Working with Scientists, Regulatory Affairs, and Research and Development in a collaborative manner • Mentoring/training new associates

🎯 Requirements

• Bachelor’s degree in medical laboratory sciences, biology, chemistry, or another relevant scientific discipline required • Minimum of two (2) years of scientific or technical writing experience strongly preferred • Knowledge of Good Documentation Practices (GDP) and regulated environments, including CLIA, CAP, and GLP preferred • Experience authoring, revising, and maintaining controlled documents such as SOPs, test records, validation reports, validation protocols, and summary reports preferred • Authorization to work in the United States indefinitely without restriction or sponsorship • Minimum of 6 years of experience in a dedicated Technical Writing role for BioPharma Technical Writer II • Strong organizational skills, with the capacity to manage multiple priorities simultaneously while maintaining accuracy and consistently meeting client deadlines • Demonstrated excellence in technical writing, grammar, editing, and document review

🏖️ Benefits

• Excellent full-time benefits including comprehensive medical coverage, dental, and vision options • Life and disability insurance • 401(k) with company match • Paid vacation and holidays