Associate Technical Writer

Kymanox is seeking an Associate Technical Writer with a strong background in FDA-regulated environments to author and revise high-quality, compliant documentation.

Requirements

• Author, revise, and format controlled documents
• Collaborate with client subject-matter experts
• Ensure traceability, consistency, and compliance with regulatory requirements
• Manage document review/approval cycles
• Participate in client meetings and present drafts

Benefits

• Hourly rate is commensurate with experience, qualifications, and other intangibles