Technical Writer (GLP Studies – Product Safety Labs)
- Location
- Bengaluru, KA, India
- Work mode
- On-site
- Employment type
- Full-time
About the job
Company Description ENGLISH 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.
Job Description Position Summary: 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. Essential Duties and Responsibilities:
- Prepare first drafts of study protocols using approved templates and Study Director guidance.
- Coordinate the development, review, revision, and issuance of study protocols, amendments, and associated study documentation in accordance with GLP requirements and internal procedures.
- 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.
- Maintain version control and document history.
- Perform document quality reviews for consistency, formatting, references, and completeness.
- Organize study data packages for reporting, archival, and inspection readiness.
- Manage signature tracking and document routing activities.
- Collaborate with Study Directors, laboratory personnel, QA, and project teams.
- Cross-train across multiple study types to support workload demands.
- Escalate scientific interpretation or unresolved content issues to the Study Director.
- Maintain historical databases
Qualifications Basic Minimum Qualifications (BMQ): To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. Education/Experience (BMQ):
- Bachelor’s degree in Life Sciences, Technical Communication, English, or related discipline; Master’s preferred.
- 4–6 years of technical writing experience in a CRO, pharmaceutical, biotechnology, or regulated environment.
- Experience with protocols, study reports, amendments, and document control systems preferred.
- Excellent writing, editing, proofreading, and formatting skills.
Additional Information Abilities and/or Skills:
• Honest, Dependable, Demonstrated Ability to Self-Manage
- Honest, Dependable, Demonstrated Ability to Self-Manage
- Detail Oriented, Accurate, Precise
- Strong Math Skills
- Strong Organizational Skills
- Logical Thinking, Good Reasoning Ability
- Strong communication including verbal, writing, and presentation skills
- Dedication to quality, ethics, and customer service
- Ability to handle personal stress
- Mental and emotional stability and maturity
- Motivation to excel
From Eurofins's careers page (SmartRecruiters), checked 31 Oct 2026.
How to apply
- Select Apply on eurofins.com. It opens Eurofins's own application form in a new tab, run on SmartRecruiters.
- Fill in the form and upload your résumé there. Jobiwork never sees your application.
- Eurofins will reply to you directly. No real employer asks you for money to apply.
Posted 28 Sept 2026 · checked 31 Oct 2026 · Report this job