Technical Writer (GLP Studies – Product Safety Labs)

Eurofins · Healthcare & Pharma

Bengaluru, KA, India
On-site
Posted yesterday
Marketing & Communications
Full-time

About the job

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.

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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