Eurofins: Technical Documentation Specialist — 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 Documentation Specialist in Bengaluru, KA, India, under reference REF82130R. 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: 15 October 2026
• Legal Entity: CIN003 - Eurofins Pharma Services India Pvt Ltd.
• Sub-Business Line: Biopharma Product Testing
• Contract Type: Permanent
• Business Lines: Biopharma Services

Responsibilities and work described

• Position Summary: We are seeking a Document Writer (Scientific Documentation & Technical Communication) to support scientific writing outputs through coordination, technical oversight, and document lifecycle management
• This role sits at the intersection of science, communication, and project management, ensuring that scientific documentation is complete, consistent, timely, and publication‑ or audit‑ready
• While this role is not primarily responsible for authoring scientific content, it serves as a key coordinator of scientific documentation by managing reviews, integrating subject matter expert input, and ensuring document readiness within a regulated environment
• Scientific Document Coordination
• Coordination: scientific input from multiple authors, reviewers, and subject matter experts
• Tracking: document components across drafting, review, and approval stages
• Quality / delivery: consistency in scientific terminology, formatting, and messaging across documents
• Technical Communication & Quality Oversight
• Review: documents for clarity, completeness, and alignment with regulatory or client expectations
• Identify gaps, inconsistencies, or unresolved comments and drive resolution
• Quality / delivery: document outputs meet internal quality standards and external regulatory requirements
• Project & Timeline Management
• Development: and manage document timelines to support project milestones
• Monitoring: document readiness and proactively escalate risks to delivery
• Interface with project teams to align documentation activities with testing, study, or submission schedules
• Cross ‑Functional Collaboration

Essential requirements and candidate background

• Sc / M
• Pharm with 5-7 years of experience)
• Experience coordinating technical or scientific documentation
• Familiarity: regulated environments (GMP, GxP, clinical research, or equivalent)
• Written communication skills with attention to detail and consistency
• Manage multiple deliverables and competing priorities

Preferred experience and additional strengths

• Preferred Qualifications (M
• Scientific or technical discipline (e.g. CCIT/Package Testing preferred, Chemistry, Biology, Life Sciences, Engineering)

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 Documentation Specialist vacancy is not an offer for reference REF82130R; 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 REF82130R.

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: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

• GMP
• GxP
• audit
• compliance
• project management
• communication
• clinical research
• chemistry