Technical Writer
Kelly Engineering is currently seeking a Technical Writer for a long-term (1+year) Hybrid contract at one of our Global clients in Irvine, CA. This role is a full-time, fully benefited position. As a Kelly employee, you will be eligible for Medical, Dental, 401K and a variety of other benefits to choose from. You'll also be eligible for paid time off, including holiday, vacation and sick/personal time. All Kelly employees receive annual performance reviews.
As a Technical Writer placed with Kelly, you will be responsible for the following:
Communicating effectively in both oral and written communication. Builds a partnership with customers by regularly demonstrating a high level of expertise and professionalism. Works as part of a team by contributing to executing Procedure Changes and Data Systems changes. Company goals, offering input and pursuing new ideas. Support Engineers with preparing technical documents, quality system reports, data systems, procedure writing, interpreting regulations, redlining and manuals. Explain complex information clearly and concisely and work with scientific staff to ensure accuracy of product descriptions. Responsible for documenting and managing change requests and executing changes in quality systems.
Duties & Responsibilities
Writes and edits technical materials such as changes in quality systems, data systems changes, reports of research findings, regulations in technical areas, technical manuals, specifications or scripts on technical subjects.
Technical documents, quality, data systems, procedure writing, interpreting regulations, redlining.
Provides written and oral reports, abstracts, summaries, charts, graphs, or other products.
Develops information and analysis to select and present information on the specialized subject in a format and at a level suitable for the intended audience.
Analyzes and review the preparation and organization of complex research. Prepares written documents, including reports, articles, formal proposals, memoranda, and formal correspondence.
Edits reports and assists in or directs the development and presentation of the information.
Analyzes changes to various projects and prepares reports of changes for review.
Organizes and coordinates assignments that involve complex, novel or obscure problems and/or special requirements for analyzing and organizing information.
Performs other related duties as assigned. This position may require occasional travel.
Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
Qualifications:
Minimum of 5 years of Technical writing in the Medical device industry.
Must be confident utilizing Microsoft Office and familiar with PLM- Product Lifecycle Management.
A Bachelor's Degree in a relevant field.