Quality Assurance Director / Sr. Director (GVP/PV)
Bridgebio
213,700 - 280,000 / year
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Description
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.
Company Overview
BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients. Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
Our focus on scientific excellence and rapid execution aims to translate today’s discoveries into tomorrow’s medicines. We have U.S. offices in San Francisco, Palo Alto, and Raleigh, with small satellites in other parts of the country. We also have international offices in Montreal, Canada, and Zurich, Switzerland, and are expanding across Europe.
To learn more about our story and company culture, visit us at bridgebio.com.
What You’ll Do
The Director / Senior Director, Quality Assurance is responsible for managing and overseeing the Good Pharmacovigilance Practices (GVP) quality and compliance program at Eidos Therapeutics and other assigned BridgeBio affiliate companies. It requires strong judgement skills and business acumen in order to advise internal and external key stakeholders on interpretation and compliance with FDA, EMA, MHRA and international pharmacovigilance (PV) regulations/guidelines; corporate policies; and standard operating procedures (SOPs). This individual will be a lead point of contact in the preparation and management of GVP regulatory inspection activities.
Responsibilities
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Provide strategic and operational guidance to the organization, including, drug safety/pharmacovigilance, medical affairs, regulatory, commercial, clinical operations and outsourcing functions, to align with company procedures, regulatory requirements and best practice
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Support the internal and external GVP audit program
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Oversee audit schedule and the execution of the audit program
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Lead or co-lead auditor on PV audits as needed
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Review and/or approval of audit reports and corrective and preventive action (CAPA) responses
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Maintain and contribute of audit and quality data for the Pharmacovigilance System Master File (PSMF)
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Core GVP regulatory inspection team member
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Lead or participate in inspection readiness activities
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Host or support of regulatory inspections
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Perform quality review of inspection requests
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Oversee the development and tracking of regulatory responses/commitments
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Review of Quality Agreements and PV/Safety Data Exchange Agreements (PVA/SDEA) to assess quality standards and regulatory compliance requirements
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Participate in the investigation and assessment of PV/GxP-related quality events and provide input on proposed CAPAs
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Develop, generate and present PV quality/compliance metrics for trending and process improvement
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Provide quality oversight on PV-related computer system validation projects and maintenance of systems
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Collaborate with Eidos and BridgeBio affiliate companies to develop and continuously improve processes and systems, including policies, SOPs and training plans
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Partner cross-functionally to support the business with compliance or quality issues/concerns by ensuring appropriate evaluation, mitigation and escalation to Executive Management
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Keep abreast of changes in regulations and enforcement actions and make recommendations for changes to policies and practices as needed
Where You’ll Work
This is a hybrid role and will require in-office collaboration in our San Francisco Office.
Who You Are
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Bachelor’s degree with 10-15+ years of GVP quality and compliance experience within a biopharmaceutical company, or contract research organization
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Current knowledge of global GVP regulations and guidelines – US Code of Federal Regulations, EMA, MHRA, and ICH Guidelines
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Ability to engage in cross-functional interactions with internal and external staff
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Has a comprehensive understanding of current approaches in industry and the ability to incorporate them into Eidos and BridgeBio affiliate programs
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Applies strong analytical and business communication skills
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
- Market-leading compensation
- 401(k) with employer match
- Employee Stock Purchase Program (ESPP)
- Pre-tax commuter benefits (transit and parking)
- Referral bonus for hired candidates
- Subsidized lunch and parking on in-office days
Health & Well-Being
- 100% employer-paid medical, dental, and vision premiums for you and your dependents
- Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
- Fertility & family-forming benefits
- Expanded mental health support (therapy and coaching resources)
- Hybrid work model with flexibility
- Flexible, “take-what-you-need” paid time off and company-paid holidays
- Comprehensive paid medical and parental leave to care for yourself and your family
Skill Development & Career Paths:
- People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
- We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
- We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
By applying, you acknowledge that BridgeBio will process your personal information as described in our Global Candidate Privacy Notice.
Benefits
- health insurance
- 401(k)
- paid time off
- stock options
- parental leave
- professional development
- bonus
About this role
BridgeBio is seeking a Quality Assurance Director or Senior Director to lead Good Pharmacovigilance Practices (GVP) compliance and quality oversight across Eidos Therapeutics and other affiliate companies. This contract role sits at the intersection of regulatory strategy and operational execution, requiring someone who can advise leadership on FDA, EMA, MHRA, and international PV regulations while managing audit programs, inspection readiness, and quality systems. You'll be a core member of the regulatory inspection team, overseeing audit schedules, reviewing corrective actions, maintaining compliance documentation, and driving process improvements across drug safety, medical affairs, regulatory, and commercial functions.
The ideal candidate brings 10–15+ years of GVP quality and compliance experience in biopharmaceutical or CRO settings, with current expertise in global regulations and ICH guidelines. You'll need strong analytical and communication skills to partner cross-functionally, assess quality events, and present compliance metrics to leadership. This role demands both strategic judgment—advising on regulatory interpretation and policy changes—and hands-on execution, from leading audits to reviewing quality agreements and supporting system validation projects.
Based in San Francisco with hybrid flexibility, this position offers a competitive salary range of $213,700–$280,000 plus performance bonus, equity, and health benefits. It's suited for someone who thrives in a fast-paced biotech environment focused on rare disease and genetic therapies, where you'll help translate scientific breakthroughs into compliant, life-changing medicines.
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Pay for this role
$213,700 to $280,000 per year
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