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

 

Submit Resume

To apply for this job email your details to info@clinlabstaffing.com