Technical Writer

2 hours ago

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Description

• Produce customer-facing product documentation such as user guides and instructions for use (IFUs) • Manage cross-functional communication to distill technical information into clear documentation • Support documentation updates for EU MDR, FDA, and other regulatory requirements • Collaborate with writers and stakeholders while managing multiple projects • Develop documentation for regulatory submissions and maintain design documentation for quality processes

Requirements

• Bachelor's degree • Minimum of 2 years of communications, labeling, and/or technical writing experience • Advanced degree with 0 years of experience is also acceptable • Exceptional writing and communication skills • Excellent problem-solving skills • Self-directed and highly organized • Strong attention to detail and accuracy • Experience working with cross-functional project teams • Experience authoring in XML within a content management system • Experience creating content for software or apps and managing software documentation projects • Experience using product lifecycle management (PLM) software • Demonstrated ability to meet deadlines and manage multiple priorities • Ability to work effectively across disciplines to implement creative solutions • Knowledge of Medtronic products and quality systems • Knowledge of formal reviews and system validation processes • Knowledge of software technologies used for writing, publishing, and document control • Knowledge of structured writing and minimalism • Aptitude to learn new requirements, processes, and tools • Understanding of industry trends in technical communication, information architecture, and content development • 2+ years of experience as a technical/medical writer in the medical device or regulated industry

Benefits

• Competitive salary • Flexible benefits package • Short-term incentive program

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