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Manager, QA Operations
qafull-timeRemote - United States
SALARY
Not listed
WORK TYPE
hybrid
JOB TYPE
full-time
INDUSTRY
healthcare
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About the role
What You'll Do
The Manager, QA Operations will serve as the primary quality owner for commercial packaging operations at assigned contract service providers (CSPs). You will ensure GMP compliance across day-to-day operations, manage batch record review and disposition activities, and serve as the quality partner to internal and external stakeholders. The ideal candidate brings expertise in commercial packaging and release operations, with a background that includes process validation and product launch support.
Responsibilities
- Serve as the quality lead for commercial packaging operations at assigned CSPs, providing oversight across primary/secondary packaging, labeling, and serialization to ensure GMP and GDP compliance.
- Review executed batch records and compile batch documentation packages to support lot disposition and market release.
- Provide quality review of deviations, change controls, CAPAs, and risk assessments related to packaging operations.
- Review and provide quality input on tech transfer, process validation, and shipping qualification protocols and reports through preparation, execution, and closure.
- Communicate/escalate manufacturing deficiencies/non-conformances to management, present issues during escalation, and work with CMOs to ensure timely resolution.
- Support review of CMC sections and regulatory filings.
- Author, review, and maintain QA Operations SOPs and controlled documents.
Where You'll Work
This is a hybrid role and requires in-office collaboration 2-3x per week in our San Francisco Office or a U.S.-based remote role that will require quarterly, or as needed visits to our San Francisco Office.
Who You Are
- Bachelor’s degree in a scientific discipline with 6+ years of experience within a biopharmaceutical company and at least 4+ years in Quality Operation roles in a current Good Manufacturing Practices (cGMP) environment.
- Strong working knowledge of FDA regulations (21CFR, 210/211), ICH guidelines, and global regulations (EU Directives, and ROW) and expertise.
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