Regulatory Program Manager, Health
Confirmed on the employer's own hiring board on Nov 14, 2026. First seen by Alion on Nov 2, 2026. Apple scores A on the Alion truth index.
Our ever-evolving suite of health and wellness products are helping our users live more active, healthier lives. Be ready to make something great when you come here. Dynamic, inspiring people and innovative, industry-defining technologies are the norm at Apple. The people who work here have reinvented and defined entire industries with our products and services. The same dedication to innovation also applies to our approach to health - strengthening our commitment to leave the world better than we found it.
This role collaborates with regulatory, quality, clinical, marketing, and engineering teams to push health features to global launch. You will connect across diverse teams and drive new regulated health features, which have the potential to improve health outcomes for people around the world.
Description
The Program Manager will provide regulatory and quality support for regulatory submissions, product launches, design changes, and policy engagements. You will collaborate closely with multiple teams to drive global product launch, including regulatory submissions, design changes, and external engagement support. In addition, you will drive day-to-day program activities and timelines, generate and own reporting, and conduct risk assessments to meet overall program objectives.
Minimum Qualifications
Bachelor's degree (BS) in Engineering, Biomedical Science, or equivalent science degree
8+ years of program/project management experience in a regulated industry, preferably in medical products and/or digital health
Proven track record of driving regulatory submissions, quality system updates, regulator engagements, and launches with multi-disciplinary teams
Outstanding communication and organizational skills, with the ability to optimally manage multiple projects simultaneously
Excellent analytical and problem-solving capabilities, with a keen eye to detect and mitigate risks
Independent self-starter who thrives in ambiguous environments
Hands-on experience in the use of project management and reporting software
Ability to be onsite weekly; this role is a hybrid, in-person position.
May require occasional travel
Preferred Qualifications
Master's degree (MS) in Engineering, Biomedical Science, or equivalent science degree
Direct hands-on experience with Design Controls and Quality Systems
Solid understanding of the regulatory process for different classes of medical devices in both the United States and international jurisdictions