Technical Writer

Location: Bay Area, USA
On-site: Palo Alto
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Position Type: Full-Time
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Company Overview:
Subsense is a pioneering organization specializing in developing innovative nanotechnology solutions aimed at revolutionizing the field of noninvasive daily used Brain-Computer Interfaces and treating Neurodegenerative disease. We are committed to creating cutting-edge products that address complex health challenges and improve customer and patient outcomes.

Job Summary:
Technical Writer will play a crucial role in documenting our technological advancements and supporting regulatory compliance. His work will ensure that both internal teams and future users have clear, concise, and accurate documentation.

Key Responsibilities:

• Create detailed technical documentation for product development, including specifications, user manuals, and installation guides
• Develop and manage a comprehensive knowledge base to capture methodologies, best practices, and key learnings
• Write and update standard operating procedures (SOPs), technical reports, and white papers
• Work with product managers, engineers, regulatory specialists, and the IP team to gather information and ensure consistency across all documents
• Work closely with the R&D team to document research findings, experimental procedures, and technical specifications
• Support the regulatory specialist by preparing and maintaining documents required for regulatory submissions and compliance
• Collaborate with the patent specialist to prepare and maintain intellectual property documents, including patent applications and IP management reports
• Collect feedback from internal stakeholders to continuously improve documentation quality and relevance
• Ensures the technical accuracy and clarity of the content for conferences

Qualifications:

• Bachelor’s degree in Engineering, Life Sciences, or a related field
• Proven experience as a Technical Writer, preferably in the MedTech or healthcare industry
• Strong understanding of technical concepts and the ability to translate them into user-friendly documentation
• Proficiency in documentation tools such as Microsoft Office, Adobe FrameMaker, MadCap Flare, or similar
• Excellent written and verbal communication skills
• Ability to work independently and as part of a team in a dynamic, fast-paced environment
• Familiarity with regulatory requirements and standards in the medtech industry is a plus
• Experience with intellectual property documentation is a plus
• Fluent in written and spoken English

What We Offer:

• Competitive salary and benefits package
• Opportunity to work in a dynamic and innovative environment
• Support for professional development and continuous learning
• Collaborative and inclusive company culture