Technical Writer, Implant

Job Description & Responsibilities:

We are hiring an experienced technical writer to join the Implant team. This role involves working closely with engineering groups to manage and deliver various documents, including SOPs, work instructions, engineering/scientific data reports, device change descriptions, and patient-facing materials.

• Deliver coherent, efficient outputs that exhibit extraordinary attention to detail in both technical and grammatical accuracy
• Collaborate across teams (e.g., Robot, Implant, BCI, Regulatory, Quality, and Clinical) to ensure accurate and timely delivery of high-quality documents
• Interpret and distill engineering documents into clear and concise written work product for technical and non-technical audiences. 
• Simultaneously manage multiple overlapping projects at different stages and on separate development programs and contribute to overall process improvement
• Maintain document history and manage version control of documents
• Conduct comprehensive literature and data searches of external and internal sources, including literature from journals, to support various documents and regulatory submissions.

About You:

• You find large challenges exciting and enjoy discovering and defining problems as much as solving them.
• You deliver. You enjoy thoughtful conversations about problems and perfecting designs, but in the end, you know that what matters is delivering quality solutions every time.
• You are a cross-disciplinary team member. You are excited to work with and learn from software, mechanical, electrical, materials, biological engineers, and neuroscientists. You are comfortable communicating across teams.
• You are resourceful, flexible and adaptable; no task is too big or too small.
• You are rigorous in thought and communication. 

Required Qualifications:

• Bachelor’s Degree in science, engineering, writing, or journalism
• 4+ years of experience in technical writing
• Demonstrated ability to swiftly grasp and effectively communicate (verbal and written) scientific and engineering concepts.
• Relentless attention to detail and quality, including fact-checking, logical flow, formatting, proofreading, and document structure.
• Evidence of driving projects (individual or team projects) from concept to completion independently.

Preferred Qualifications: 

• Hands-on engineering or programming experience.
• Familiarity with hardware, software, and firmware development and production.
• Prior experience writing user and/or system documentation.  
• Experience with medical device best practices and regulatory requirements for FDA and/or international bodies.