At Mojo, we're inventing the future of computing - Invisible Computing - which imagines a world where information is there when you need it, technology fades away, and you can freely connect with others in a more meaningful and confident way. Our team includes talented professionals with expertise in product design, user experience, applied physics, hardware, software, optics, photonics, electronics, chemistry, biology and vision science. Together, we're building Mojo Lens, a smart contact lens with a built-in display that gives you timely information without interrupting your focus. Mojo Lens elevates your vision by providing the information you need exactly when it's needed - all while letting you look like you.
We are a well-funded startup founded by technology experts with decades of experience developing pioneering products and platforms and backed by some of the world's leading technology investors. We are located in Saratoga, CA.
Assist with the preparation and maintenance of new and existing regulatory applications including investigational and marketing applications (e.g. 510(k)s, De Novos, PMAs, etc.), amendments, supplements, and other submissions in compliance with health authority regulations
Assess the acceptability of quality, preclinical and clinical documentation for premarket submission filing
Compile, prepare, review and submit regulatory submission to authorities; interact with regulatory to answer questions in a timely manner
Provide strategic input, technical and compliance guidance on regulatory requirements to project teams and other regulatory personnel
Utilize technical regulatory skills to propose strategies on complex issues
Maintain associated regulatory files for related projects
Gather medical device data from databases and literature searches
Interact with various regulatory agencies, contract groups, and partner organizations, as needed
Work closely with clinical to ensure protocols and analytical plan will provide appropriate data to support regulatory submission
Monitor applications under regulatory review
Communicate application progress to all appropriate departmental personnel
Monitor impact of changing regulations on submission strategies and update all appropriate departmental personnel
Develop and maintain regulatory processes and SOPs to ensure compliance with latest applicable regulations
Assist with label development and review for compliance before release
Support product registration and post-approval activities
Organize plan for compliance with product post-marketing approval requirements, maintaining annual licenses, registrations, update Technical Files / Design Dossiers
BA/BS degree, preferably in a scientific field.
10 years of experience in the device/biopharmaceutical industry, including 5 year in a regulatory affairs-medical devices role.
Ability to contribute to strategic development in regard to regulatory approach for premarket products (FDA, EU, APAC)
Confident writer, able to organize and draft documents with little or no previous samples
Excellent organizational, multitasking, and communication skills.
Strong attention to detail, organization and accuracy
Proficiency with MS Office suite, Adobe Acrobat
Experience on project teams (new product development) with submissions to regulatory bodies
Comfortable working independently and as part of a team on multiple projects with ability to prioritize effectively
If solving challenging problems and shaping the future interests you, come join us at our offices in Saratoga, CA just outside of San Jose. Along with competitive compensation employee perks include flexible time off, access to full health benefits and a stocked fridge and pantry in the office. Even if you don't see your dream job on our openings page, you can still apply for it with the "Create your own position" option.