VP, Regulatory Affairs, Strategy, Labeling and Operations

Who you are

You have extensive experience in regulatory affairs, ideally with a background in biopharma or related industries. You possess strong leadership skills and have successfully managed teams focused on regulatory operations and compliance. Your strategic mindset allows you to align regulatory activities with business objectives, ensuring excellence in all submissions and labeling processes. You are familiar with integrating advanced technologies, such as artificial intelligence, to enhance operational efficiency and insight. You thrive in environments that challenge convention and encourage innovative thinking. You are passionate about making a difference in the biopharma industry and are excited about the opportunity to lead a team of experts.

What you'll do

As the Vice President of Regulatory Affairs, you will oversee the Operations and Labeling functions at BridgeBio. You will manage a team of subject matter experts responsible for ensuring compliance and excellence across all regulatory activities. Your role will involve developing and implementing regulatory strategies that align with the company's goals, while also ensuring that the organization has the necessary infrastructure and technology to support global submissions. You will work closely with cross-functional teams to drive strategic alignment and ensure that all regulatory activities are executed efficiently. Additionally, you will be responsible for integrating advanced capabilities, such as artificial intelligence, into regulatory processes to enhance efficiency and insight. You will play a key role in shaping the future of regulatory affairs within the organization, pushing boundaries and redefining what is possible in biopharma.

What we offer

At BridgeBio, you will be part of a pioneering team that is redefining the biopharma landscape. We offer a competitive salary range of $335,000 to $390,000 USD, along with comprehensive benefits. You will have the opportunity to work in a hybrid environment, with flexibility to work remotely or from our San Francisco or Washington DC offices. We foster a culture of innovation and collaboration, where your ideas and contributions will be valued. Join us in our mission to develop life-changing medicines for patients with unmet needs and make a significant impact in the industry.