BridgeBio Pharma

Compensation

Full 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. Affiliate 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, which causes 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 The Manager/Sr. Manager of GMP QA Manufacturing provides on-the-floor quality oversight for GMP manufacturing activities related to API and Finished Drug Product. This role ensures compliance with global regulatory standards (21 CFR Parts 210/211, EU GMP, ICH Q7, ICH Q10) and internal quality systems, while supporting efficient and compliant product release. The Manager/Sr. Manager reviews and approves executed batch records, deviations, investigations, change controls, and associated documentation. They make quality recommendations on the release of API and finished products, ensuring that only compliant materials meeting all specifications are released for use or distribution. Responsibilities 1. GMP Oversight and Compliance Provide real-time QA oversight during manufacturing, packaging, labeling, and testing activities for API and Finished Drug Product Ensure that production operations comply with approved batch records, SOPs, and GMP regulations Perform line clearance, in-process checks, and review of critical operations Support internal and external audits, regulatory inspections, and readiness programs 2. Batch Record Review and Product Release Review executed batch production and laboratory control records for completeness, accuracy, and compliance Assess and verify that all critical process parameters and quality attributes are met prior to batch release Ensure all associated documentation (deviations, change controls, investigations, analytical results, environmental monitoring, etc.) is resolved and approved before release Recommend or approve release of API and Finished Drug Product for commercial or clinical use in alignment with the Qualified Person (QP) or Responsible Person (RP) where applicable Maintain product disposition documentation within the electronic Quality Management System (eQMS) 3. Deviation and Investigation Management Lead or review deviations, out-of-specification (OOS), and non-conformance investigations Ensure thorough root cause analysis and implementation of effective CAPAs Evaluate potential product impact and support decision-making on product disposition 4. Change Control and Continuous Improvement Review and approve manufacturing-related change controls to ensure risk assessments and validation requirements are appropriately addressed Identify opportunities for process and system improvement through trend analysis and quality metrics Support implementation of Quality Risk Management principles in daily operations 5. Cross-Functional Collaboration Collaborate with Manufacturing, QC, Supply Chain, Technical Operations, and Regulatory Affairs teams to ensure timely and compliant manufacturing operations Provide quality input during production planning, tech transfers, process validation, and process performance qualification (PPQ) Participate in cross-functional quality review boards and risk assessment teams 6. Documentation and Training Ensure manufacturing documentation (batch records, SOPs, forms) is current, accurate, and approved per QA procedures Where You’ll Work This a U.S-based remote role that will require quarterly, or as needed visits to our San Francisco Office and to our global vendors and/or partners as needed. Who You Are Education: Bachelor’s degree in Chemistry, Biology, Pharmacy, Chemical Engineering, or related scientific discipline Experience: 7+ years of experience in GMP Quality Assurance or Manufacturing within the pharmaceutical or biopharmaceutical industry Minimum 3 years in a QA review/release capacity (API and/or finished drug product) Strong understanding of cGMP, ICH, and global regulatory requirements Experience with contract manufacturing oversight and batch release processes Skills: Excellent attention to detail and technical writing skills Strong communication and decision-making abilities Proficiency with eQMS systems (e.g., Veeva, TrackWise, MasterControl) Demonstrated ability to interpret complex quality data and make sound, compliant decisions Ability to build relationships and work collaboratively with a variety of individuals within the department, company, and external vendors A strong team player with the ability to effectively communicate sound quality advice cross-functionally based on experience, regulations, and business needs 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: Market leading compensation 401K with 100% employer match on first 3% & 50% on the next 2% Employee stock purchase program Pre-tax commuter benefits Referral program with $2,500 award for hired referrals Health & Wellbeing: Comprehensive health care with 100% premiums covered - no cost to you and dependents Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions) Hybrid work model - employees have the autonomy in where and how they do their work Unlimited flexible paid time off - take the time that you need Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents Flex spending accounts & company-provided group term life & disability Subsidized lunch via Forkable on days worked from our office 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, Spring Health & BetterUp Coaching 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 $141,000—$181,993.75 USD