Technical Writer

Summary

• Compile and analyze experimental data.
• Write,create, draft, edit, review and maintain technical protocols and reports.

Essential Duties and Responsibilities include, but are not limited to, the following:

• Creates and maintains technical writing standards.
• Writes, modifies/changes controlled documents.
• Writes, reviews, and maintains department standard operating procedures.
• Edit, standardize, or make changes to materials prepared by other writers or personnel.
• Coordinates projects and documentation assignments.

Basic Qualification

• BS/BA degree in science, engineering, or Technical Writing with a concentration in science, engineering, or applied technology fields required.
• 5+ years of experience within the medical device/biotechnology industry
• Experience in drafting Design Documentation, including:
  • M.E.A., U.R.S., F.R.S., D.I.D.O., Risk Management Plans/Reports, P.M.S. Reports.

Other experience:

• Good documentation practices (GDP)
• FDA/GMP regulated environments