Senior Technical Writer page is loaded## Senior Technical Writerlocations: Cork, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R552381Work Flexibility: Hybrid or OnsiteThis is a permanent role with full Stryker benefits.**What you will do:**Supports product teams by independently developing product instructional materials for complex medical devices or product lines. Deliverables may include - product instructions for use, Quick Guides, online help, and other product-related customer facing documentation and analysis of usability of these deliverables. Audience includes physicians, healthcare staff, facility engineers, and patients for a global audience. Deliverables must comply with medical device regulations, standards, and business requirements**KEY AREAS OF** **RESPONSIBILITY*** Develop customer facing product instructional information for an entire business unit according to user needs and regulatory requirements for domestic and international customers.* Interface cross-functionally within the product development team to acquire source materials and to develop understanding of the products.* Interview and collect information from Subject Matter Experts (SMEs) from R&D, RA, various functional areas.* Write and edit Instructions For Use (IFUs), Quick Start Guides and other accompanying documents aligning content with associated product labels.* Participate in new product development meetings with cross functional team members to capture inputs, project deliverables and product specifications.* Effectively plan and track workload and projects understanding the critical path and interdependencies in a multi-project environment while effectively communicating timelines with project teams.* Manage multiple assignments for complex projects to meet project milestones.* Collaborate with the Graphic Designer to incorporate graphical elements for instructional purposes and accurate interpretation and international application.* Drive and assist with departmental continuous improvement endeavors.* Review and edit on the work of others prepared work within functional area.* Trains members of our functional team.* Provide reviews of regulatory documentation to ensure that medical device labeling references are complete and correct and compliant with FDA and EU requirements.* Manage IFUs PLM/CMS system for controlled releases and revision management.* Complete applicable QMS documentation as required by the regulatory and change management process.* May own NCs/CAPAs as needed.* May assist with regulatory audits.* Participate and own improvement projects on the team.**What you will need:*** Bachelor's degree required (English, Technical Writing, Technical Communication, Communication, or related curriculum preferred.* 2+ years applicable Technical Writing experienceTravel Percentage: 10%
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