Principal International Regulatory Affairs Associate

Role Number: 200643237-0836 Summary Our ever-evolving suite of Health and Wellness products for iPhone and uf8ffWatch is 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. That same spirit of innovation drives our Health projects, where cross-functional teams collaborate closely to explore ambitious ideas in their earliest stages. Our dedication to innovation also extends to our business practices, strengthening our commitment to leave the world better than we found it.The uf8ff Health group is looking for an experienced Regulatory Affairs professional with global expertise to lead a special project involving large-scale, multi-functional collaboration across Apple. If you are passionate about the health space and want to make a meaningful impact here at Apple, this could be the role for you. We are a lean, collaborative organization that works closely across multiple teams. We care deeply about getting amazing new products into our customersu2019 hands. Description You will represent the International Regulatory Affairs team on a high-impact, collaborative project. In partnership with regional RA experts, you will develop, articulate, and drive the global regulatory strategy for innovative pipeline features. You will proactively address regulatory challenges, make informed decisions, and communicate appropriate regulatory actions. Additionally, you will develop engagement strategies with global health authorities to facilitate the regulatory pathway and support launch plans as needed. Key responsibilities include:u2022 Develop and implement comprehensive global regulatory strategies for Apple Health featuresu2022 Collaborate closely with multi-functional teams across Apple to communicate regulatory plans clearly and maintain alignment throughout developmentu2022 Lead and handle regulatory authority interactions and negotiations, advocating for Appleu2019s position while ensuring compliance and timely approvalsu2022 Identify potential regulatory risks and opportunities early by engaging with global regulatory landscapes, and advise internal teams to inform product development and strategyu2022 Partner with internal partners and external bodies to influence and shape emerging regulations and guidances that impact Apple Health initiatives.This is site-based role. Minimum Qualifications + Bacheloru2019s degree or equivalent in science or engineering + 10+ years of experience in regulatory affairs + Regulatory expertise in one or more key markets such as EU/UK, China, or Japan + Proven ability to work autonomously and drive established goals and initiatives with minimal supervision + Executive presence and poise, demonstrated through a strong track record of positively influencing decisions and cross-functional teams Preferred Qualifications + Masters / PhD / post-secondary education preferred + Experience working with the SaMD product and wearable technology + Experience navigating regulatory environment in emerging markets + Excellent verbal and written communication skills Apple is an equal opportunity employer that is committed to inclusion and diversity. We seek to promote equal opportunity for all applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, Veteran status, or other legally protected characteristics. Learn more about your EEO rights as an applicant (.

Created: 2026-03-07