Technical Writer I - Process Development
Core
Authoring, reviewing, and maintaining critical scientific and manufacturing documentation (reports, protocols, certificates) for biologics development and manufacturing programs.
Role type
Entry-level technical writer (process development)
Builds
Scientific and manufacturing documentation supporting client programs and internal operations
Domain
Biopharmaceuticals / Biologics manufacturing
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Scientific writing, technical editing, proofreading, cross-functional collaboration, GMP documentation compliance, data integrity, Microsoft Office proficiency
Preferred skills
Life sciences degree, regulated environment experience, client-facing documentation, process improvement
Responsibilities
Author and edit technical reports and protocols; Review documents for accuracy and compliance; Collaborate with scientists and quality teams; Manage multiple documentation projects; Support client-facing technical reports
Seniority
Entry-level, hands-on IC
