Associate Director/Director, Regulatory Affairs CMC
BridgeBio
Associate Director/Director, Regulatory Affairs CMC
BridgeBio
Develops therapies for genetic diseases
Mavericks Wanted
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on
In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.
Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.
POSITION DESCRIPTION
Job Title: Associate Director/Director, Regulatory Affairs CMC
Reports to: Executive Director, Regulatory Affairs CMC
This regulatory professional will have demonstrated the ability to work independently under the direction of his/her manager. This individual will manage internal regulatory processes, prepare documents for regulatory submissions in compliance with global health authority regulations. In conjunction with regulatory affairs leadership, he/she will develop strong relationships, collaborate, and interact with various departments and levels of management, including interactions across BridgeBio subsidiaries. Furthermore, the successful candidate will have demonstrated knowledge of regulatory requirements and guidelines and be able to apply their knowledge to daily work, and as needed represent regulatory affairs CMC as part of an interdisciplinary team.
REMOTE – This is a U.S.-based role that will require quarterly, or as needed visits to our San Francisco Office.
Responsibilities include but are not limited to the following:
Develop global CMC regulatory strategies in collaboration with manager and CMC subject-matter experts to meet business objectives for the Eidos program
Collaborate with cross-functional teams (e.g. Regulatory Int.) to create and prepare CMC sections of regulatory dossiers marketing applications (ROW)
Help prepare and communicate timelines
Plan and coordinate preparation of the CMC sections
Manage the author, review and approval workflows
Provide recommendations to team on regulatory strategy as needed
Provide RA CMC support for Health Authority interactions, including coordination of drafting and reviewing meeting requests and briefing books.
Work with team on strategy and responses to Health Authority CMC questions (ROW)
Provide support from triage through finalization of regulatory responses
Provide input to team on regulatory strategy as needed
Maintain current knowledge of applicable global regulations, guidance and standards for drug development and product registration
Other duties as assigned.
Qualifications
A minimum of a bachelor’s degree is required (life sciences discipline preferred)
Minimum of 7 years experience in pharmaceutical or related industry in regulatory affairs, CMC or related function, eg, drug development/manufacturing/QC/QA (an equivalent combination of education and experience may be considered)
Excellent communication skills and attention to detail
Independently able to manage projects and deliver output in a timely manner with limited direction of manager
Excellent computer skills, e.g., Microsoft suite of applications/software and document management system such as Veeva
Demonstrated self-starter with the ability to take initiative, work independently, and proactively identify and execute tasks with minimal supervision.
Excellent interpersonal, active listening, and influencing skills
Demonstrated ability to leverage artificial intelligence tools to support and enhance the execution of complex tasks, improving efficiency, and decision-making quality.
As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.
For BridgeBio Full-Time U.S Based Roles:
Financial & Rewards
Health & Well-Being
Skill Development & Career Paths:
By applying, you acknowledge that BridgeBio will process your personal information as described in ourGlobal Candidate Privacy Notice.
Salary 190000 - 285000 USD
BridgeBio Pharma develops medicines for genetic diseases using a decentralized subsidiary model, where each subsidiary focuses on a specific disease while sharing central resources. It advances multiple drug programs at once by leveraging genome sequencing, molecular biology, and patient data to translate research into therapies that target underlying genetic causes. The company differentiates itself through its independent subsidiary structure with centralized support, combined with data-driven decision making and a culture of transparent, evidence-based testing. Its goal is to bring effective, disease-modifying therapies to patients faster by advancing a diverse pipeline from discovery to commercialization through partnerships and eventual approval.
Explore more opportunities at BridgeBio