Design Quality Technical Writer II

Boston Scientific • Maple Grove, MN

5d

About The Position

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.

Requirements

• 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

Responsibilities

• Develop and maintain design history files
• Develop and maintain risk management file deliverables (e.g., Hazard Analysis, DFMEA)
• Develop and maintain post-market surveillance deliverables
• Develop and maintain 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level