Senior Regulatory Program Manager

Oracle•United States,

7d•$79,100 - $166,100•Remote

About The Position

At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large global health companies require experienced regulatory leaders who can navigate complex and fast-changing regulations, and public policies across the globe. In this context, we are looking for a program manager in the medical device software and healthcare regulatory space, who will be leading actions that concern this broad array of opportunities globally. With his/her organizational expertise and business acumen, he/she will play a pivotal role in driving Oracle's success and competitiveness in the healthcare and life sciences sector. As Program Manager on the Health and Life Sciences Legal and Compliance Team, you will work in collaboration with Product teams and subject matter experts to compile, track, and organize the required documentation to register products in global markets where the products are sold. This role requires an individual who can keep up with the fast-paced environment of software development and an evolving regulatory landscape. For this role we are seeking a program manager who is collaborative and creatively resolves problems to drive operational excellence across the Medical Device Regulatory Affairs department. Special consideration will be given to applicants with experience with Regulatory and/or Quality processes. Only Oracle brings together the data, infrastructure, applications, and expertise to power everything from industry innovations to life-saving care. And with AI embedded across our products and services, we help customers turn that promise into a better future for all. Discover your potential at a company leading the way in AI and cloud solutions that impact billions of lives.

Requirements

Experience navigating complex and fast-changing regulations and public policies globally.
Ability to keep up with the fast-paced environment of software development and an evolving regulatory landscape.
Collaborative and creative problem-solving skills.
Organizational expertise and business acumen.

Nice To Haves

Experience with Regulatory and/or Quality processes.

Responsibilities

Compile, track, and organize the required documentation to register products in global markets where the products are sold.
Lead actions that concern a broad array of opportunities globally in the medical device software and healthcare regulatory space.
Drive operational excellence across the Medical Device Regulatory Affairs department.
Collaborate with Product teams and subject matter experts.