About BridgeBio
Bridging science and hope for genetic diseases
Key Highlights
- Public company (NASDAQ: BBIO) with strong market presence
- Over 15 drug development programs targeting rare genetic diseases
- $1.5B+ raised from top investors like OrbiMed
- Headquartered in Palo Alto, California
BridgeBio (NASDAQ: BBIO) is a biopharmaceutical company headquartered in Palo Alto, California, focused on developing innovative medicines for genetic diseases. With a pipeline of over 15 programs, BridgeBio aims to address unmet medical needs for rare genetic conditions, leveraging advancements in ...
🎁 Benefits
BridgeBio offers competitive salaries, equity options, comprehensive health benefits, and generous PTO policies. Employees also enjoy a flexible work ...
🌟 Culture
BridgeBio fosters a culture of innovation and collaboration, emphasizing the importance of scientific rigor and entrepreneurial spirit. The company va...
Compliance Manager • Lead
Skills & Technologies
Overview
BridgeBio is seeking a Vice President of Regulatory Affairs to oversee operations and labeling functions while supporting regulatory strategy. You'll manage a team of experts and integrate advanced capabilities like artificial intelligence. This role requires extensive experience in regulatory affairs.
Job Description
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.
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