Eurofins Scientific is seeking candidates for a Technical Documentation Specialist / Document Writer (Scientific Documentation & Technical Communication) position in Bengaluru, Karnataka. The role focuses on scientific document coordination, technical communication, quality oversight, and document lifecycle management within a regulated scientific environment.
Candidates with a master’s degree in a science or technical discipline and experience coordinating scientific or technical documentation can apply for this opportunity.
Eurofins Scientific Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Eurofins Scientific |
| Job Title | Technical Documentation Specialist |
| Position | Document Writer – Scientific Documentation & Technical Communication |
| Location | Bengaluru, Karnataka, India |
| Job Type | Full-time |
| Qualification | Master’s degree in any science field |
| Preferred Background | Scientific or technical disciplines, including Chemistry, Biology, Life Sciences, Engineering, and CCIT/Package Testing |
| Work Environment | Regulated scientific, laboratory, or clinical research environments |
Position: Technical Documentation Specialist
The selected candidate will coordinate scientific documentation across authors, reviewers, and subject matter experts. The role involves ensuring document consistency, completeness, quality, and readiness for publication, audits, or regulatory submissions.
The position primarily focuses on documentation coordination and oversight rather than independently authoring scientific content.
Key Responsibilities
1. Scientific Document Coordination
- Coordinate scientific input from authors, reviewers, and subject matter experts.
- Track documents through drafting, review, and approval stages.
- Maintain consistency in scientific terminology, formatting, and messaging.
2. Technical Communication and Quality Oversight
- Review documents for clarity, completeness, and alignment with regulatory or client expectations.
- Identify documentation gaps, inconsistencies, and unresolved comments.
- Ensure deliverables meet internal quality standards and external regulatory requirements.
3. Project and Timeline Management
- Develop and manage documentation timelines aligned with project milestones.
- Monitor document readiness and escalate delivery risks.
- Coordinate documentation activities with testing, study, and submission schedules.
4. Cross-Functional Collaboration
- Coordinate between scientific, quality, regulatory, and client-facing teams.
- Support structured handoffs between authors, reviewers, and document coordination teams.
- Communicate document status, timelines, and expectations clearly.
Eligibility and Qualifications
Candidates should meet the following requirements:
- Master’s degree in a science field.
- Background in a scientific or technical discipline, such as Chemistry, Biology, Life Sciences, or Engineering.
- CCIT/Package Testing experience or knowledge is preferred.
- Experience coordinating technical or scientific documentation.
- Familiarity with regulated environments, including GMP, GxP, clinical research, or equivalent settings.
- Strong written communication skills with attention to detail and consistency.
- Demonstrated ability to manage multiple deliverables and competing priorities.
Experience in CROs, GMP laboratories, clinical research, or regulated scientific environments is strongly preferred.
Required Skills
Applicants should demonstrate the following abilities:
- Scientific documentation coordination and technical communication.
- Strong organisational and project management skills.
- Accuracy, precision, and attention to detail.
- Logical thinking, reasoning, and mathematical skills.
- Strong verbal, written, and presentation skills.
- Ability to work independently and manage competing priorities.
- Commitment to quality, ethics, and customer service.
- Dependability, self-management, and professional maturity.
- Ability to handle work-related stress.
- Ability to sit for extended periods as required by the role.
Relevant Professional Backgrounds
The job description identifies the following backgrounds as relevant to this position:
- Technical Project Manager
- Clinical Project Coordinator
- Scientific Program Manager
- Client Technical Liaison
Professionals with experience coordinating documentation across scientific, quality, regulatory, and project teams may find this role relevant to their background.
How to Apply
