Location: St. Paul, MN
Duration: 9+ months

Position Description

Position is to create work instructions, release work instruction, drawings, and related product documentation in the windchill document control system. Completes (template based) biocompatibility protocols and reports in conjunction with SME guidance

Qualifications

  • Experience with Windchill Product Data Management systems required
  • Experience writing and facilitating change orders / ECO’s required
  • 5+ years’ related work experience within the Medical Device Industry required
  • Previous experience or related work experience as a technical writer preferred
  • Knowledge of ISO 10993 standards for biocompatibility strongly desired
  • Experience communicating with cross-functional teams
  • Excellent writing, editing, analytical, and organizational skills
  • Computer proficient in Word, EXCEL, PowerPoint, etc.,
  • Associate or bachelor’s degree in science related field

 

 

Click to submit a resume or find additional support.