Technical Writer (GLP Studies – Product Safety Labs)
BengaluruFull-time4–6 yrsPosted 1 week ago
Mid-level content and media role at Eurofins in Bengaluru. Needs 4–6 years.
About the role
The Technical Writer supports the preparation, revision, formatting, control, and organization of study documentation associated with GLP-compliant preclinical research. The role enables Study Directors to focus on scientific interpretation and regulatory accountability.
What you'll do
- Prepare first drafts of study protocols using approved templates and Study Director guidance
- Coordinate the development, review, revision, and issuance of study protocols, amendments
- Prepare report sections, narratives, tables, and appendices from approved source data
- Create shell reports, templates, and standardized study documents
- Coordinate document review cycles, comment resolution, and final issuance
What you need
- GLP
- Writing
- Technical writing
- Editing
- CRO
- Proofreading