Senior Program Manager, Biotech – CMC & Cross‑Functional Lead

Dormont Manufacturing Co

San Francisco (CA)

Hybrid

USD 180,000 - 195,000

Full time

14 days+
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Benefits offered by this job

Market-leading compensation
401(k) with employer match
Employee Stock Purchase Program (ESPP)
Hybrid work model
Paid time off

Job summary

BridgeBio in California seeks a Senior Manager, Project Management to support the CMC team with cross-functional planning, risk mitigation, and proactive resource allocation. You will communicate with internal stakeholders and external partners to ensure on-time delivery of critical programs.

The role emphasizes collaboration across CDMOs, regulatory submissions, and long-range planning, with hybrid in-office work in San Francisco and generous benefits.

Qualifications

  • M.S. or B.S. in chemistry, chemical engineering or equivalent preferred.

Responsibilities

  • Organize and coordinate CMC/QA team activities and deliverables; manage weekly team meetings; prepare agendas and track action items
  • Interface and manage multiple CDMOs to drive manufacturing activities in alignment with CMC timelines and clinical and commercial supply needs
  • Draft sections of regulatory filings and coordinate cross-functional reviews; organize document QC processes for content accuracy
  • Contribute to long-range and budgetary planning; collaborate with Legal and Finance to manage vendor contracts and POs
  • Effectively manage multiple responsibilities and deliverables concurrently

Skills

Delivering in fast-paced environment
Strategic planning
Cross-functional collaboration
Time management
Independent work

Education

M.S. or B.S. in chemistry or chemical engineering

Job description

BridgeBio in California seeks a Senior Manager, Project Management to support the CMC team with cross-functional planning, risk mitigation, and proactive resource allocation. You will communicate with internal stakeholders and external partners to ensure on-time delivery of critical programs.

The role emphasizes collaboration across CDMOs, regulatory submissions, and long-range planning, with hybrid in-office work in San Francisco and generous benefits.

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