Technical Writer - IV

Position Title: Technical Writer

Work Location: St. Paul, MN, USA 55117

Assignment Duration: 6 Months

Work Schedule: Mon - Friday Daytime hours

Work Arrangement: 100% Onsite

Research, write, edit technical documentation to support new and sustaining product development projects.

Support documentation efforts for new and sustaining product development projects within our organization.

* Research, write, edit technical documentation to support new and sustaining product development projects.

* Collaborate with development engineering, marketing, regulatory affairs, and clinical, among others, to gather inputs for IFUs.

* Follow internal processes and procedures.

* Understand and comply to medical device regulatory requirements related to labeling.

* Technical aptitude for learning new tools and systems.

* Ability to work in a fast-paced and changing environment.

* Experience / familiarity releasing documentation in Document Control system.

* Very high-level attention to detail.

* Requires a Bachelor's Degree in a relevant technical discipline, Communications, Science, English or equivalent.

* Must have a minimum of two to six plus years of progressively more responsible experience as a technical writer in a medical or high-technology (preferably biotechnology) environment.

* Experience working in a content management system required.

* Must have current or recent medical device or pharma industry experience.

* Must have 2-6 years of experience in the medical device industry.

* Must have end-user technical writing experience; that is, direct experience writing clinician and/or patient manuals.

* Attention to detail

* Self-starter, manage own projects, no handholding

* Learns tools quickly; content management a plus

* Able to juggle multiple projects at once

* Working with project teams