Design Quality Technical Writer II

Your responsibilities will include: Develop and maintain design history files, risk management file deliverables (e.g., Hazard Analysis, DFMEA), post-market surveillance deliverables, and other technical documents for interventional cardiology and vascular therapy medical devices. Manage the release and revision of version-controlled documents in the BSC document management system. Work closely with cross-functional teams including Regulatory Affairs, Research & Development, and Clinical Risk to gather information and ensure accuracy of technical content. Bachelor's degree in Technical Writing, English, Communications, Engineering, or a related field. Minimum 3 years of work experience in related field Excellent writing, editing, and proofreading skills. Ability to manage multiple projects and meet deadlines. Proficiency in document management systems and content creation tools. Strong interpersonal and communication skills. Attention to detail and commitment to producing high-quality documentation. Experience working in a regulated industry.