About Truvian Truvian is a fast-paced, disruptive healthcare company at the intersection of diagnostics and consumer technology. We’re building a fully automated, benchtop diagnostic system that delivers lab-accurate results from a small blood sample in just 30 minutes. Designed for retail clinics and private practices, our platform is currently undergoing FDA review and aims to revolutionize routine blood testing by making it more accessible, affordable, and actionable. At Truvian, our mission goes beyond the lab. We are committed to empowering individuals with timely health data and fostering a culture of innovation, collaboration, and discovery. Join us and help realize our vision of transforming routine health testing for today’s connected consumers. Position Summary Truvian is seeking an experienced and hands-on Regulatory Affairs Director to lead and execute all aspects of the company’s global regulatory strategy. This leadership role will be responsible for supporting regulatory submissions and product registrations across domestic and international markets, ensuring compliance with applicable regulations, and enabling timely product commercialization. The ideal candidate must have extensive experience in the in vitro diagnostics (IVD) industry, with a strong track record of leading both FDA 510(k) and CLIA Waiver submissions through to successful clearance. This individual will work cross-functionally with internal stakeholders, regulatory bodies, and international partners to ensure our technology meets all applicable
requirements while aligning with Truvian’s mission to transform diagnostic testing. This position is onsite and reports to the Head of Quality & Regulatory. This is a high-impact, hands-on role based at our corporate headquarters in San Diego, California. Key
Responsibilities Support the regulatory strategy for Truvian’s portfolio of IVD products, ensuring proactive planning and timely execution of submissions to FDA (510(k), CLIA Waiver), Health Canada, European Notified Bodies (CE Mark/IVDR), and other international agencies. Support the end-to-end regulatory submission process, including the development of submission dossiers, gap assessments, pre-submissions, and agency interactions. Work with the regulatory team to ensure a comprehensive regulatory roadmap aligned with product development and commercialization milestones. Provide regulatory guidance during all phases of product development, from concept through design transfer, clinical validation, and market launch. Ensure all product documentation, including labeling, advertising, and promotional materials, meets regulatory
requirements. Interpret and communicate complex regulatory
requirements to internal stakeholders in a clear and actionable manner. Support regulatory impact assessments of product and process changes; oversee documentation updates and change control. Monitor and implement evolving global regulatory
requirements (e.g., IVDR transition, ISO 13485 updates) and translate them into internal strategies and processes. Support post-market regulatory activities, including vigilance reporting, field actions, and annual reporting obligations. Collaborate with OEMs, distributors, and international partners to align global regulatory strategies and support international market entry. Required
Qualifications Bachelor’s degree in Life Sciences, Engineering, or a related discipline required; advanced degree (MS, PhD) strongly preferred. 12+ years of experience in Regulatory Affairs, with a minimum of 8 years in the IVD industry. Proven success leading and managing FDA 510(k) and CLIA Waiver submissions and approvals; experience with De Novo submissions is a plus. In-depth knowledge of U.S. FDA regulations, CLIA
requirements, EU IVDR, ISO 13485, and other global regulatory standards relevant to IVDs. RAC certification preferred (U.S., Global, or EU). Demonstrated ability to translate complex regulatory guidance into practical regulatory strategies. Experience interfacing with regulatory bodies, including preparation for and participation in agency meetings and audits. Strong organizational, project management, technical, and analytical skills, with a high level of attention to detail. Exceptional verbal and written communication skills, including the ability to influence and lead cross-functional teams. Proficiency in Microsoft Office Suite; experience eQMS required. What You’ll Love About Working Here At Truvian, we’re more than just a diagnostics company — we’re a mission-driven team committed to transforming the way people access and experience blood testing. Here's what makes working with us truly special: Impactful Mission : Join a passionate team revolutionizing point-of-care blood diagnostics and making a tangible difference in healthcare access. High-Energy Environment : Thrive in a fast-paced, high-growth startup that values innovation, collaboration, and purpose. Comprehensive
Benefits Package , including: Medical, Dental, Vision, and Life Insurance Flexible Paid Time Off (PTO) and Paid Parental Leave 401(k) plan with generous company match Wellness
Perks : On-site gym and fitness classes Access to a farm-to-table café with a 30% employee discount Kombucha, cold brew, and healthy snacks are always on tap Supervisory Role No Travel
Requirements May require up to 10% travel FLSA Exempt Work Location Onsite Salary Range $168,000 - $186,000 This range considers the wide range of factors that are considered in making
compensation decisions, including but not limited to experience, skills, knowledge, abilities, education, licensure and certifications, and other business and organizational needs. Salary offers are determined based on final candidate
qualifications and experience. Placement within the
compensation range is determined by level, band, internal equity, and relevant
qualifications Physical Demands Ability to lift and move up to 5 lbs. Frequently standing and sitting for long periods. Visual
requirements include close, distance, color, peripheral, and depth perception. Application Instructions We want to hear your story! To apply, please submit your resume and a cover letter outlining your experience and what excites you about joining Truvian. Equal Opportunity Employer Truvian is an Equal Opportunity Employer. We are committed to building a diverse and inclusive team where everyone belongs and thrives. All employment decisions are made based on
qualifications, merit, and business needs — never based on race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, age, or veteran status.
