Brandon founded Vectis in 2021, leveraging expertise and network built over 15 years of experience in medical diagnostics with a focus on consumer-oriented design. As founder and CEO of Boston Microfluidics (Now Weavr Health), Brandon raised $20M+, built a strategic relationship with Labcorp to developed the first product to enable home collection with gold standard results, and contributed to over a dozen patents. In addition to his work with Vectis, Brandon currently serves as Managing Partner of Nexus Medical Labs, offering clinical lab services as well as CRO services for home-collection and home-testing providers, and Co-Chair of the Home Testing Special Interest Group of the American Telemedicine Association. Client service specialties include company setup, strategic planning, fundraising & partnerships, design for manufacture, and regulatory approvals.

Molly leads the team and manages operations at Vectis, leveraging over a decade of experience building impact-focused companies and managing cross-functional teams. She served most recently as co-executive director of a pandemic response organization, Open Source Medical Supplies, and managed entrepreneurial ecosystem-building and organizational leadership programming on three continents for MIT D-Lab. In addition to her executive leadership and management experience, Molly leverages her years as an educator & facilitator to help teams clarify and communicate a shared vision and resolve conflict.

Client service specialties include company setup, strategic planning, project & platform management, recruiting & hiring, team management, communications and messaging.

Bethany is an award-winning entrepreneur, multidisciplinary designer, and product and materials technologist. She has over 8 years of hands-on diagnostic test kit development experience and 10+ years of consumer insights and branding expertise.  

As the inventor and founding CEO of Lia Diagnostics, developers of the first FDA cleared plastic-free, compostable and flushable pregnancy test, Bethany’s invention and work helped pioneer the field of water-dispersible, biodegradable diagnostic test kits; she holds over 80 patents related to Lia’s novel design.

In addition to her work with Vectis, Bethany supports the World Business Council for Sustainable Development in partnership development with a focus on Circular Economy and Health, is a member of the Fast Company Executive Board, and is an advisor for Springboard Enterprises' companies. 

Bryan is a proven executive covering high-tech and medical device biotech C-suite functions with 23 years
across high tech verticals, focusing on entrepreneurial programs with success in identifying new opportunities
and obtaining consensus with key decision-makers.
As a co-founder of Qorvo Biotechnologies, Bryan spent the last 10 years growing it from conception into a
fully operating revenue-generating company with 95 employees, including a recent business sale. As General
Manager, Bryan led the establishment of asset acquisitions, IP licensing, development of world-class technical teams, global high-volume manufacturing establishment, government funding engagements, and go-to-market strategy.
Bryan holds Masters Degrees in Business and Electrical Engineering from Babson College, and Oregon Health
and Science University respectively, and undergraduate degrees in Biology and Biochemistry from the
University of Portland.

Jill is a senior level leader with over 25 years of business experience. She has been focused since 2009 on building clinical programs and leading US and global clinical trials in the Biotech, Pharmaceutical, Medical Device and Tissue Industries. Her specialties include strategic planning, clinical trial development, protocol design, trial execution, data management, building clinical infrastructure, implementing quality processes and preparation of regulatory submissions.

Kaela is an experienced clinical research & operations manager. Before this work, she spent almost a decade in microdevice design and fabrication, biological sample handling and experimental design. Her specialties include clinical research, clinical trial design and management, analysis of clinical data, microdevice fabrication via soft photolithography, dielectrophoresis, human erythrocytes, electrokinetics, lab on a chip devices.

Lee brings executive experience in clinical diagnostics, laboratory medicine, healthcare regulations, and FDA regulatory and compliance.  He has worked extensively in laboratory, hospital, and health system operations, including process improvement, service line development, strategic initiatives, and growth strategies. Lee also has served in executive roles for medical device manufacturers leading new product and service line development in conjunction with bioassay/device research and development and sponsored clinical trials and investigations. Lee also has designed, developed, and led organizational change strategic initiatives for physician practices, corporations and health systems that were focused on collaboration, culture, and quality. In addition to his significant industry experience, he has served in various capacities in higher learning from lead faculty, program director to course and online learning environment development.

With nearly 30 years of service in the In-vitro Diagnostics industry, Lucius (Tad) Fox, PhD, has developed over 75 IVD products for use in both human and veterinary medical applications. His experience spans all aspects of the product design and manufacturing process development including technology innovation, design, and manufacturing process development. His contributions to the IVD industry span a broad range of applications including new and existing diagnostic markers in Clinical Chemistry, Therapeutic Drug Monitoring, Drugs of Abuse, Proteins, Diabetology, Kidney Injury, Infectious Diseases, Hormones, Lipids, Liver Markers and Hemostasis (Coag). Tad has broad experience leading and developing R&D organizations in both startup & large scale companies. With a passion for design efficiency and product integrity, he uses systems engineering approaches across all projects to ensure the creation effective product designs and robust manufacturing processes. He has served on several ISO and CLSI initiatives to create new industry wide standards and has solid experience interacting with regulatory agencies. Tad holds a PhD in Physical Chemistry from the California Institute of Technology is active both as an expert medical device consultant and university instructor.

With 25 years of business experience and 15 years in the biotechnology industry designing, developing, and launching medical devices and diagnostic products, Michael (Cappy) Cappillino has helped numerous companies deliver value faster while improving their ability to effectively manage risk and investment. Teams leverage his expertise as a strategic business leader, product and assay developer, data scientist, Project Management Professional, Lean Six Sigma Green Belt, and graduate of the Isenberg School of Management to help teams efficiently plan and execute all manner of projects, including organizational design, strategic planning, new product introduction, process improvements, regulatory affairs, quality management, operational excellence, and more.

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Dr. Josh Buser is a scientist, engineer, and toolmaker focusing on biomarker quantification solutions for the past 15 years. He specializes in early-stage medical device technology development and transfer to manufacturing. His innovations have resulted in 8+ patent applications. His technical skills include microfluidics, supply chain development, laminate manufacturing for point-of-care diagnostics, fluid dynamics in porous media, non-electric precision temperature control, along with microscopy and quantitative image analysis. Josh performed his PhD and postdoc work at the Univ. of Washington Dept of Bioengineering, and holds a B.S. in Mechanical Engineering from the Univ. of Wisconsin-Madison.

Josh Beckmann combines a diverse background in small scale manufacturing, public health research, and prototyping. He currently specializes in applying simple technologies to novel medical device applications. His technical skills include: CAD design/rendering, digital fabrication, and electronic prototyping and fabrication. He holds a Masters of Public Health and Masters of Social Work from Boston University and a Bachelor of Arts in Sociology from University of Minnesota.

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With over 20 years of experience in leadership positions in the pharmaceutical industry working with groups providing bioanalytical support and technological innovation for the quantitative determination of drugs, metabolites and biomarkers in biofluids, Neil has successfully applied his knowledge and skills to helping companies to integrate biological fluid microsampling and patient centric sampling and analysis into workflows. He also works with innovator companies to develop technologies and introduce them to the market. Neil also assists organisations with their understanding of emerging trends in the pharmaceutical industry and bioanalysis.

WIth over 40 years of experience in medical diagnostics, the last 20 as a principal biostatistician in the in vitro diagnostic industry, Dr. Jeffrey Budd has helped companies across the globe to develop hundreds of products and file their successful submissions to FDA, EU and other national regulators. As an ongoing leader and key contributor in multiple organizations (Clinical and Laboratory Standards Institute, International Organization for Standardization, International Federation of Clinical Chemists) he remains at the forefront of the IVD industry with respect to standardization, product development, and validation.