Job Posting: Technical Documentation Specialist
Core
Coordinate scientific documentation lifecycle, manage reviews, and ensure document readiness for publication or audit in regulated environments.
Role type
Senior IC scientific document coordinator
Builds
Publication-ready and audit-ready scientific documentation
Domain
Life sciences / Regulated environments (GMP, GxP, clinical research)
Required skills
Scientific or technical discipline, Document lifecycle management, Regulatory environment familiarity, Cross-functional collaboration, Timeline management, Quality oversight
Preferred skills
CRO experience, GMP laboratory experience, Clinical research experience, Technical project management background
Technologies
None stated
Responsibilities
Coordinate scientific input from multiple authors and subject matter experts, Track document components across drafting and review stages, Review documents for clarity and regulatory alignment, Develop and manage document timelines, Act as liaison between scientific, quality, and client teams
Seniority
Mid-level, hands-on IC
