TytoCare works with leading health plans and providers worldwide, to roll out Home Smart Clinic solutions that enable accessible, high-quality primary care from home, with no compromises. The Home Smart Clinic solutions include remote physical exams that work across primary care modalities, and can be tailored to any cohort or population. Together with Tyto Insights™️ AI-powered guidance, provider integrations, and Tyto Engagement Labs™️ which include member journeys and engagement frameworks, Home Smart Clinic solutions ensure more equitable access to care across the globe, and enable healthcare organizations to meet their KPIs.

Co-founded by Dedi Gilad and Ofer Tzadik in 2012, TytoCare has FDA and CE clearances and partners with over 220 major health systems, health plans, and strategic partners in the U.S., Europe, Asia, Latin America, and Israel.

This is a temporary position for a 8 month contract (with a long term option).

Responsibilities

• Completion of documentation requirements necessary for timely product releases with special attention to ISO, FDA, CE, and company requirements.
• Collaborate with cross-functional teams to assist in the implementation of design control activities throughout the product development life cycle activities.
• Responsible for managing the software validation process.
• Assist in preparing documentation required for regulatory submissions, under the guidance of experienced professionals.

Requirements

• Currently pursuing a degree in biomedical engineering, biotechnology, life sciences, or a related field.
• Strong interest in quality management and design control processes.
• Excellent organizational and communication skills.
• Detail-oriented with a commitment to producing high-quality work.
• Familiarity with regulatory requirements (e.g., FDA CE and ISO) is an advantage.
• Proactive attitude and ability to work collaboratively in a team
• Excellent computer skills