Eurofins: Technical Writer (GLP Studies – Product Safety Labs) — Bengaluru, KA, India

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists Technical Writer (GLP Studies – Product Safety Labs) in Bengaluru, KA, India, under reference REF81676D. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Department: Testing & Laboratory
• Employment type: Full-time
• Employer listing date: 28 September 2026
• Legal Entity: CIN003 - Eurofins Pharma Services India Pvt Ltd.
• Contract Type: Permanent
• Business Lines: Other Business Line
• Brands: Eurofins

Responsibilities and work described

• 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
• Preparation: first drafts of study protocols using approved templates and Study Director guidance
• Coordination: the development, review, revision, and issuance of study protocols, amendments, and associated study documentation in accordance with GLP requirements and internal procedures
• Preparation: report sections, narratives, tables, and appendices from approved source data
• Create shell reports, templates, and standardized study documents
• Coordination: document review cycles, comment resolution, and final issuance
• Maintenance: version control and document history
• Execution: document quality reviews for consistency, formatting, references, and completeness
• Organize study data packages for reporting, archival, and inspection readiness
• Management: signature tracking and document routing activities
• Collaboration: 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
• Maintenance: historical databases

Essential requirements and candidate background

• 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
• 4–6 years of technical writing experience in a CRO, pharmaceutical, biotechnology, or regulated environment
• Writing, editing, proofreading, and formatting skills

Education and qualification routes

• Degree / qualification: Master’s preferred

Preferred experience and additional strengths

• Experience: protocols, study reports, amendments, and document control systems preferred

Location, schedule and contract conditions

• Work arrangement: On-site
• Advertised location: Bengaluru, KA, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Technical Writer (GLP Studies – Product Safety Labs) vacancy is not an offer for reference REF81676D; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF81676D.

Compare your qualifications and experience with the essential conditions for the Bengaluru, KA, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: GLP

GLP-related experience should identify the laboratory activity and the controls or records you handled. Explain how work was documented, checked and traceable within the environment you actually worked in.

Relevant skills

• GLP
• clinical research
• laboratory testing
• biotechnology
• pharmacy
• communication
• document control