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About the Role
BridgeBio 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.
Responsibilities
- Lead Document Control compliance and process improvement efforts
- Manage, plan, and coordinate document control activities and processes
- Manage documentation by processing, formatting, issuing the documents for training, and making it effective accurately
- Responsible for reviewing Document Change Controls to ensure proper revision control of records and closure
- Manage document periodic review process and coordinate with the stakeholders on its completion
- Perform Business Administrator activities in the electronic document management system (Veeva QualityDocs)
- Execute user test scripts for the electronic document management system during changes to the systems
- Manage Learner Roles, curriculums, and training requirements in the Learning Management System (Veeva Training)
- Support onsite audit/ and or in any regulatory inspections
- Perform other projects related to improvement of quality systems as needed and required by management
- Other duties as assigned
Requirements
- Bachelor’s degree or higher
- Minimum 5-10 years of experience in a quality assurance role in the pharmaceutical industry required
- Experience with EDMS and LMS systems, preferably Veeva Quality Docs and Veeva Training
- Excellent knowledge and understanding of applicable GxP regulations
- Experience in the identification and resolution of Good Documentation Practices issues
- Familiarity with Microsoft Office Suite, Adobe Pro, etc.
- Ability to work in a fast-paced environment with excellent multi-tasking skills
- Must have attention to detail
- Works with minimal supervision
- Must have effective technical writing skills
- Requires excellent organizational, interpersonal, and communications skill
- Must exhibit professional behavior and be aware of the importance of teamwork within the assigned department
- Ready to embrace BridgeBio’s core values and diverse corporate culture
Skills
- Veeva QualityDocs
- Veeva Training
- Microsoft Office Suite
- Adobe Pro
- Technical writing
- Organizational skills
- Interpersonal skills
- Communication skills
Location
- San Francisco Office
Work Type
- Hybrid
Experience Level
- 5-10 years
Education Level
- Bachelor's degree or higher
Salary/Compensations
- $135,700—$185,000 USD
Benefits
- 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
- 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)
- 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
- Career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
- Financial rewards, peer-to-peer recognition, and growth opportunities
About the Company
- 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.