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Technical Writer II in Valencia, CA. at TPS Family of Companies

Date Posted: 2/28/2018

Job Snapshot

Job Description

Duties and tasks expectations to perform on a daily/regular basis:

•Co-author or contribute to the creation and revision of medical device labeling deliverables, specifically Directions for Use

•Clearly and correctly state and summarize technical information and conclusions in instructional labeling

•Make suggestions or corrections in order to make instructional labeling more clear and concise

•Review and peer-edit the work of other writers to ensure high quality standards within the technical writing group

•Interface cross-functionally within the product development team - and throughout the company - to acquire source material/information for instructional labeling, and to develop understanding of the products and the product development process

•Experience creating content within the confines of a department style guide

Job Requirements

Quality Systems Duties and Responsibilities:

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

Education/Experience/Skills a candidate must have to successfully perform the above duties/tasks:

•2+ years of experience working as a technical writer within the technology or medical device field •Demonstrated ability to author content using a department style guide

•Experience creating medical device instructions for use

•Bachelor’s degree

•Experience using InDesign to create medical device labeling deliverables

•Experience authoring using department style guides

•Demonstrated knowledge of structured writing

•Experience working under the guidance of standard operating procedures governing the development of medical device products

 Education/Experience/Skills that are not required, but helpful:

•Bachelor degree in Scientific and Technical Communications, or technical writing certification

•Advanced degree in a health sciences or a scientific field of study