Location: Bay Area, USA
On-site: Palo Alto
Position Type: Full-Time
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