Design Quality Technical Writer I

Relevant regulatory standards (e.g., FDA, ISO), and other global medical device regulations (e.g., MDR). Content Management: Manage the release and revision of version-controlled documents in the BSC document management system. Collaboration: Work closely with cross-functional teams including Regulatory Affairs, Research & Development, and Clinical Risk to gather information and ensure accuracy of technical content. Editing and Proofreading: Review and edit documentation for clarity, grammar, and style, ensuring consistency across all materials. Incorporate feedback from stakeholders to continuously improve documentation quality and usability. Bachelor's degree in Technical Writing, English, Communications, Engineering, or a related field Excellent writing, editing, and proofreading skills Internship, academic project, or coursework experience related to Technical Writing Experience working in a regulated industry Ability to manage multiple projects and meet deadlines Proficiency in document management systems, such as Windchill, and content creation tools Strong interpersonal and communication skills Attention to detail and commitment to producing high-quality documentation