Manager, Finished Goods Labeling
BridgeBio
June 25, 2026
Remote friendly (San Francisco, CA)
United States
Operations
What You’ll Do
You will be responsible for the commercial product labeling creation and maintenance for a growing portfolio of products and global markets, partnering cross-functionally with CMC, Supply Chain Operations, Quality Assurance, and CMC-Regulatory Affairs. Serve as a key point of contact for labeling process issues. Own a labeling and artwork management system (GLAMS), including training others and maintaining the system.
Responsibilities
- Coordinate creation, revision, review, and approval of product labeling (carton/container labels and artwork components).
- Manage labeling workflows and document control in Perigord GLAMS with Veeva RIM impacts.
- Maintain labeling version control, archival records, and audit-ready documentation.
- Support regulatory submissions involving labeling changes for the U.S., EU, and other global markets.
- Track labeling change requests and ensure timely implementation across stakeholders.
- Collaborate with Regulatory Affairs to ensure labeling aligns with FDA, EMA, and other global regulatory requirements.
- Coordinate cross-functional reviews with Medical, Safety, Clinical, Quality, Legal, and Commercial teams.
Where You’ll Work
Hybrid role; in-office collaboration 2–3x/week in San Francisco (remote candidates may be considered).
Who You Are
- Bachelor’s degree in a scientific, regulatory, or related field.
- Direct hands-on experience using Perigord GLAMS label management system (required).
- Experience coordinating labeling activities for pharmaceutical/biotechnology products.
- Working knowledge of U.S. FDA labeling regulations; familiarity with EU/international labeling requirements.
- Experience supporting labeling updates across multiple products or programs.
- Strong organizational skills; able to manage multiple labeling projects simultaneously.
Benefits (U.S. full-time)
- Market-leading compensation; 401(k) match; ESPP; pre-tax commuter benefits; referral bonus; subsidized lunch/parking.
- Employer-paid medical/dental/vision; HSA with employer contributions; FSA; fertility/family-forming benefits; mental health support; flexible PTO; paid medical and parental leave.
Salary
$153,000 - $176,000 USD
You will be responsible for the commercial product labeling creation and maintenance for a growing portfolio of products and global markets, partnering cross-functionally with CMC, Supply Chain Operations, Quality Assurance, and CMC-Regulatory Affairs. Serve as a key point of contact for labeling process issues. Own a labeling and artwork management system (GLAMS), including training others and maintaining the system.
Responsibilities
- Coordinate creation, revision, review, and approval of product labeling (carton/container labels and artwork components).
- Manage labeling workflows and document control in Perigord GLAMS with Veeva RIM impacts.
- Maintain labeling version control, archival records, and audit-ready documentation.
- Support regulatory submissions involving labeling changes for the U.S., EU, and other global markets.
- Track labeling change requests and ensure timely implementation across stakeholders.
- Collaborate with Regulatory Affairs to ensure labeling aligns with FDA, EMA, and other global regulatory requirements.
- Coordinate cross-functional reviews with Medical, Safety, Clinical, Quality, Legal, and Commercial teams.
Where You’ll Work
Hybrid role; in-office collaboration 2–3x/week in San Francisco (remote candidates may be considered).
Who You Are
- Bachelor’s degree in a scientific, regulatory, or related field.
- Direct hands-on experience using Perigord GLAMS label management system (required).
- Experience coordinating labeling activities for pharmaceutical/biotechnology products.
- Working knowledge of U.S. FDA labeling regulations; familiarity with EU/international labeling requirements.
- Experience supporting labeling updates across multiple products or programs.
- Strong organizational skills; able to manage multiple labeling projects simultaneously.
Benefits (U.S. full-time)
- Market-leading compensation; 401(k) match; ESPP; pre-tax commuter benefits; referral bonus; subsidized lunch/parking.
- Employer-paid medical/dental/vision; HSA with employer contributions; FSA; fertility/family-forming benefits; mental health support; flexible PTO; paid medical and parental leave.
Salary
$153,000 - $176,000 USD