Technical Writer (GLP Studies – Product Safety Labs)

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  • Full-time
  • Bengaluru, KA, India
  • Testing & Laboratory
  • 10d ago

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


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