Job Summary

A staffing agency is seeking a Virtual Technical Writer.

Core Responsibilities of this position include:

• Working with complex technical writing, editing, and documentation issues following cGMP regulations
• Working alongside team to ensure all quality findings are correct

Skills and Requirements Include:

• Proficient with document management systems, quality systems, and document collaboration systems
• Condor, Veeva, and SmartSheets
• Expert level use of Google Software, Microsoft Office, and Visio
• 3+ years of Technical Writing experience in a regulatory environment
• Experience in biotech or pharmaceutical manufacturing
• cGMP experience