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Technical Writer
EurofinsBioPharma Technical Writer responsible for creating and maintaining technical documentation for validation activities in a life sciences company. Collaborating with experts to ensure compliance and quality standards.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in technical writing and documentation within regulated environments, including proficiency in Good Documentation Practices (GDP) and experience with standard operating procedures (SOPs) and validation reports. Strong organizational skills and the ability to collaborate effectively with cross-functional teams are essential.
Highest-signal resume keywords
Technical Writing ExperienceGood Documentation Practices (GDP)Controlled Document ManagementRegulatory Compliance KnowledgeBachelor’s Degree in Relevant Discipline
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Technical WritingDocument ReviewEditingSOP AuthoringValidation Report PreparationProtocol DevelopmentGrammar ProficiencyContent AnalysisDocument RevisionScientific Writing
Soft Skills
Organizational SkillsCollaborationMentoringTrainingTime Management
Industry Keywords
CLIACAPGLPBioPharmaLaboratory OperationsQuality InitiativesContinuous ImprovementCross-Functional CollaborationValidation ProtocolsTechnical Documentation
About the role
Key responsibilities & impact- Developing, reviewing, and maintaining controlled documentation that supports validation and laboratory operation activities
- Ensuring that standard operating procedures (SOPs), forms, protocols, and other technical documents are accurate, clear, and compliant
- Collaborating with cross-functional subject matter experts to manage documents, support quality initiatives, and promote consistency and continuous improvement
- Writing and editing forms, protocols, reports, and procedures from existing templates under supervision
- Analyzing documents to maintain continuity of style and content
- Performing updates and revisions to technical documents as instructed
- Working with Scientists, Regulatory Affairs, and Research and Development in a collaborative manner
- Mentoring/training new associates
Requirements
What you’ll need- Bachelor’s degree in medical laboratory sciences, biology, chemistry, or another relevant scientific discipline required
- Minimum of two (2) years of scientific or technical writing experience strongly preferred
- Knowledge of Good Documentation Practices (GDP) and regulated environments, including CLIA, CAP, and GLP preferred
- Experience authoring, revising, and maintaining controlled documents such as SOPs, test records, validation reports, validation protocols, and summary reports preferred
- Authorization to work in the United States indefinitely without restriction or sponsorship
- Minimum of 6 years of experience in a dedicated Technical Writing role for BioPharma Technical Writer II
- Strong organizational skills, with the capacity to manage multiple priorities simultaneously while maintaining accuracy and consistently meeting client deadlines
- Demonstrated excellence in technical writing, grammar, editing, and document review
Benefits
Comp & perks- Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays