Our ever-evolving suite of Heath and Wellness products for iPhone and Watch 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 business practices -strengthening our commitment to leave the world better than we found it.

The  Health group is looking for a Global Regulatory Policy Lead to oversee advocacy efforts for Apple’s medical devices features, globally. 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 organization who works closely together to establish relationships across multiple functional teams. We care deeply about getting amazing new products into our customers hands.

You will lead Apple’s global medical device policy in medical devices and represent the Health team on a diverse array of initiatives and programs, with the goal of marketing new technologies. You will work closely with partners across Health, including Regulatory, Clinical, Government Affairs and other organizations, to pave the way for innovative health features in new and existing geographies. You’ll oversee and lead Apple Health’s global policy goals as well as:

• Establish the vital coalitions and teams to advocate for expanding Apple’s presence in health, globally.

• Lead and support regulatory policy efforts internationally.

• Build, scale and develop international policy programs, including processes, resources and tools.

Bachelor’s degree or equivalent in a life science, legal or business subject area.10+ years of medical device experience in a regulatory role or working in government, with at least 5+ years as a senior manager, director or equivalent within a medical device company or government position.Significant experience in leading interactions with regulatory health authorities in the US and abroad.Expertise in crafting policy and advocacy positions, memos and briefing documents.