Scientific Technical Writer I - Lab Operations
Core
Create and maintain documentation supporting manufacturing processes and ensuring regulatory compliance in a pharmaceutical lab environment.
Role type
Technical Writer I (Lab Operations)
Builds
Manufacturing process documentation and regulatory compliance records
Domain
Pharmaceutical manufacturing / Life Sciences
Required skills
GMP regulations knowledge, Quality management systems, Method validation experience, Analytical technologies (HPLC, GC, UV spectroscopy), Document management systems, Microsoft Office (Word, Excel), English (advanced written/verbal)
Preferred skills
Chemistry degree, Pharmaceutical/medical device manufacturing experience, GMP/technical writing certifications
Responsibilities
Translate complex technical information into clear documentation, Collaborate with engineering, operations, and quality teams, Enter laboratory to observe processes, Manage multiple projects and meet deadlines
Seniority
Entry-level, hands-on IC
