at Apple
Location
Cupertino, United States of America
Compensation
$175k–$291k USD
Type
full time
Posted
1 weeks ago
Market range · function + seniority
p25 · target · p75 · n=296
Posted $291k · well above market
Tailor your résumé to this role in 30 seconds.
Free account · ATS keyword check · per-job bullet rewrite by Claude.
You will represent the RA/QA team on a diverse array of regulatory initiative teams and new product development, with the goal of obtaining approvals for new technologies. You will demonstrate the ability to develop a variety of solutions to regulatory challenges and will exercise independent judgment in settling and communicating appropriate regulatory action and requirements. This role will involve assessment of regulatory impact for new and modified Class I, II and III products, including identification of assumptions/risks/mitigations to develop and execute clear regulatory plans in the US and globally.
B.S. ME/EE/BME/CS degree or equivalent in any engineering discipline
10+ years of medical device experience in a regulatory role, with at least 5+ years as a principal, manager or lead.
Significant experience in leading interactions with the US Food & Drug Administration.
Significant experience preparing regulatory filings, including pre-submissions, 510(k)s, De Novos, and IDEs.
Strong working knowledge of US regulations that affect Class I, II and III devices.
Experience with Software as a Medical Device (SaMD) and algorithm- or sensor-based products, including how regulatory strategy interacts with clinical study design and algorithm performance.
Ability to be onsite; this role is a hybrid, in-person position.
Global regulatory strategy experience (e.g., EU MDR) is a strong plus.
Demonstrable background in being autonomous and being able to clearly work towards establish goals and initiatives with minimal oversight.
Working as part of a focused project team.
Proven competence in determination of appropriate global regulatory requirements for new products or product changes.
Partnering with and across engineering teams to set regulatory strategy.
Strong organizational and management skills.
Excellent communication skills, both verbal and written.
Imagine what you could do here. At Apple, excellent ideas have a way of becoming great products, services, and customer experiences. Bring passion and dedication to your job, and there’s no telling what you could accomplish. The people at Apple don’t just build products — we craft the kind of wonder that’s revolutionized entire industries.
The Health group is looking for a Principal Regulatory Affairs Associate to help drive strategy and submissions for health products. If you are passionate about the health space and want to have an incredible impact here at Apple, this could be the role for you. We are an efficient team who works closely together to build relationships across multiple functional teams. We care deeply about getting amazing new products into our customers hands. We come to Apple to think creatively about how to launch products within a rigorous regulatory structure for medical devices.
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
At Apple, we believe accessibility is a fundamental human right. You’ll find that idea reflected in everything here — in our culture, our benefits and our digital tools. By welcoming as many perspectives as possible, we help you build a career where you feel like you belong.
Learn about accessibility in Apple’s workplace
Learn about reasonable accommodations for job applicants
Apple accepts applications to this posting on an ongoing basis.
More open roles at Apple
Hiring velocity, headcount trend, and every open posting on one page.
Open postings ranked by description similarity — useful if this role isn't quite right.