Engineering Program Manager

Location: SCV

ABOUT THIS FEATURED OPPORTUNITY

The Health organization at Apple is seeking an experienced Engineering Program Manager (EPM) to join the Health Regulatory and Quality Medical Device team. This role will drive complex, cross-functional programs focused on regulated health features and medical device initiatives, ensuring compliance, quality, and successful global delivery.

THE OPPORTUNITY FOR YOU

As an Engineering Program Manager, you will lead end-to-end execution of innovative health features and medical device programs, including both new product development and feature enhancements. You will work at the intersection of engineering, regulatory, and business teams to bring high-impact health technologies to market.

Key program areas include:

• Global launch and scaling of health features (e.g., ECG and related capabilities)
• Irregular rhythm notifications and hypertension-related initiatives
• Women’s health features, including cycle tracking
• Hearing health innovations, including hearing tests and AirPods hearing aid functionality
• Sleep apnea detection and monitoring features
• Vision-related technologies, including prescription lenses for Vision Pro
• Development of Class I and Class II medical devices with varying risk profiles

KEY RESPONSIBILITIES

• Lead cross-functional program execution across engineering, regulatory, and quality teams
• Drive development timelines, deliverables, and risk mitigation strategies
• Manage Design History Files (DHF) and ensure complete, compliant technical documentation
• Act as a liaison between technical teams and business stakeholders (internal and external)
• Ensure alignment with global regulatory standards and requirements
• Coordinate product development across hardware, software, and medical domains

KEY SUCCESS FACTORS (Top 3 Must-Have Skills)

1. Deep Medical Device Program Management Experience
   • 10+ years managing programs in the medical device industry (e.g., large companies like Abbott, Medtronic, Boston Scientific, or similar environments) not Pharmaceuticals
   • Experience across project or product would be helpful
   • Strong background in Design History Files (DHF) and technical documentation
   • Proven ability to bridge technical and business teams
2. Regulatory & Quality Expertise
   • Strong knowledge of FDA regulations, EU MDR, and medical device compliance
   • Experience with SaMD (Software as a Medical Device) and/or Class II devices
3. Exceptional Communication & Stakeholder Management
   • Ability to drive alignment across diverse internal and external stakeholders
   • Strong cross-functional collaboration and executive communication skills

NICE TO HAVES

• Bachelor’s degree in a technical field (Engineering or related discipline preferred; advanced degree not required)

About INSPYR Solutions

Technology is our focus and quality is our commitment. As a national expert in delivering flexible technology and talent solutions, we strategically align industry and technical expertise with our clients’ business objectives and cultural needs. Our solutions are tailored to each client and include a wide variety of professional services, project, and talent solutions. By always striving for excellence and focusing on the human aspect of our business, we work seamlessly with our talent and clients to match the right solutions to the right opportunities. Learn more about us at inspyrsolutions.com.

INSPYR Solutions provides Equal Employment Opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, INSPYR Solutions complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.

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