Director/Sr. Director, Vendor Quality Management

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.

COMPANY OVERVIEW

QED Therapeutics, an affiliate within BridgeBio Pharma, focuses on developing targeted treatments for FGFR-driven skeletal dysplasia, particularly Achondroplasia. Achondroplasia is the most common form of genetically driven short stature and can cause potentially debilitating medical complications. With our experimental therapeutic candidate, infigratinib, we seek to provide an option for children living with Achondroplasia and their families.

WHAT YOU’LL DO

Reporting to the Vice President, Quality, the Director/Sr. Director, Vendor Quality Management provides strategic and operational leadership for the qualification, oversight, and performance management of contract manufacturers (CMOs), contract laboratories, suppliers, and service providers supporting GxP activities.

RESPONSIBILITIES

Vendor Qualification & Lifecycle Management

• Establish and maintain a risk-based vendor qualification and requalification program

• Define vendor risk classification criteria and oversight frequency

• Oversee vendor assessments and approval processes

• Monitor vendor performance through quality metrics

• Lead vendor transition or discontinuation activities as needed

Quality Agreements & Governance

• Oversee development and maintenance of Quality Agreements

• Ensure agreements clearly define roles and responsibilities

• Align Quality Agreements with business contracts

• Periodically review and update agreements

Performance Monitoring & Risk Management

• Establish vendor performance metrics

• Conduct Quality Business Reviews with key vendors

• Implement risk-based monitoring strategies

• Proactively identify and mitigate compliance risks

Inspection Readiness & Regulatory Support

• Ensure vendor oversight documentation supports inspection readiness

• Participate in regulatory inspections

• Coordinate vendor support during inspections

• Oversee remediation related to vendor findings

Cross-Functional Collaboration

• Partner with CMC, Clinical Operations, Clinical Development, Supply Chain, Commercial, Regulatory, Legal and other functions as needed

• Provide vendor compliance risk expertise during program planning

• Support new product introductions and technology transfers as needed

Continuous Improvement

• Benchmark vendor oversight practices

• Drive digital enablement of vendor management systems

• Promote proactive quality culture across partner network

WHERE YOU’LL WORK

This is a U.S.-based remote role with periodic travel to the San Francisco offices and global vendors and partners as needed.

WHO YOU ARE

• Bachelor’s degree in scientific discipline or equivalent experience

• 12+ years of pharma/biotech quality experience with vendor oversight

• Strong knowledge of cGMP and global regulatory expectations

• Experience managing vendor audit programs

• Experience drafting and negotiating Quality Agreements

• Experience supporting regulatory inspections

• Strong risk assessment and collaboration skills

• Travel: ~25–35%

Rewarding Those Who Make the Mission Possible

We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.

Financial Benefits:

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Market leading compensation

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401K with 100% employer match on first 3% & 50% on the next 2%

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Employee stock purchase program

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Pre-tax commuter benefits

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Referral program with $2,500 award for hired referrals

Health & Wellbeing:

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Comprehensive health care with 100% premiums covered - no cost to you and dependents

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Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions)

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Hybrid work model - employees have the autonomy in where and how they do their work

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Unlimited flexible paid time off - take the time that you need

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Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents

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Flex spending accounts & company-provided group term life & disability

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Subsidized lunch via Forkable on days worked from our office

Skill Development & Career Paths:

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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

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We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, Spring Health & BetterUp Coaching

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We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities

At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.

Salary
$1—$2 USD