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Technical Writer (GLP Studies – Product Safety Labs)

Eurofins · Bengaluru, KA, India

  • Pharmaceuticals & Biotech
  • 10,001+ employees
  • Luxembourg, Luxembourg

Mixed hiring record · median 47 days open

9898

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Actively hiring

Still listed on the employer's own board · How we score

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  • 43% of this employer's openings are over 60 days old

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  • Still listed on the employer's own board

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Technical Writer (GLP Studies – Product Safety Labs) at Eurofins. We’ll keep it in your applied jobs, so you can see it later and be warned before applying to the same employer twice.

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

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.

Abilities and/or Skills

  • 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

All candidate CV's and cover letter's will be reviewed, however please note that we are not always able to respond to every expression of interest submitted. Â

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