Technical Writer (GLP Studies – Product Safety Labs)

Eurofins provides analytical testing and laboratory services across life sciences and other industries. The Technical Writer prepares, reviews, controls, and organizes GLP study documentation for preclinical research.

• Draft study protocols using approved templates and Study Director guidance
• Prepare study report sections, narratives, tables, and appendices
• Coordinate document reviews, revisions, and final issuance
• Maintain document versions, history, and signature tracking
• Organize study data packages for reporting, archiving, and inspections
• Review documents for consistency, formatting, references, and completeness

Education

Bachelor's degree

Degree

life sciences, technical communication, english

Experience

4 to 6 years

Domain

life sciences testing

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