Location: Minnetonka, MN
Duration: 9 months
• Co-author or contribute to the creation and revision of Product Development Process (PDP) deliverables
• Clearly and correctly state and summarize technical information and conclusions in documents
• Organize and transform raw data into usable tables and graphs
• Make suggestions or corrections in order to make a document more clear and concise
• Plan documents and create the draft or framework of a document for the engineer or team to use as their working document
• 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 documents and to develop understanding of the products and the product development process
• Participate in department projects and/or lead portions of department projects
• Bachelor’s Degree required. Degree in technical writing or related technical field such as engineering or biology preferred.
• Must have 2+ years technical writing experience (medical device or other regulated industry preferred).
• Must have strong writing, editing, and communication skills.
• Must have expert knowledge of Microsoft Word and a working knowledge of Microsoft Excel and PowerPoint. Knowledge of Microsoft Visio desired.Preferred Qualifications:
• Must have the ability to work in collaboration with others on a project team as well as working independently on tasks.
• Must demonstrate attention to detail.
• Must have the ability and desire to keep track of document and project details.
• Must be able to work quickly and efficiently on documents and tasks while maintaining high quality in work.
• Must demonstrate proactive work habits and assertiveness in creating and owning documents.
• Must have an aptitude to understand engineering and other technical information.
• Must have project management and time management skills.
• Problem solving skills and an ability to respond and adapt to change is desired.
Quality System Requirements:
• In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
• Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the company Quality Policy.
• Establishes and promotes a work environment that supports the Quality Policy and Quality System
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