Director, Supply Chain - Commercial

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. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.

What You'll Do

You lead commercial manufacturing and packaging for our products, with a particular focus on packaging and ex-US supply. You own the external network that turns bulk drug product into a compliant, serialized, market-ready commercial pack — managing artwork, serialization, packaging validation and the CMO partnerships. This role scales in step with our commercial expansion, you will help stand up the capability, not simply inherit it.

Responsibilities

Own commercial packaging engineering — primary, secondary and serialized packaging — from design and qualification through steady-state supply, ensuring every configuration is manufacturable, compliant and patient-ready.

Lead ex-US commercial manufacturing and distribution, managing CMOs with our international affiliates, and packaging partners across international markets to meet demand, quality and regulatory requirements.

Own end-to-end artwork management.

Own serialization and track-and-trace compliance (e.g. EU FMD, DSCSA and equivalent ex-US requirements), ensuring systems, master data and partners are aligned market by market.

Lead packaging and process validation, protocols and change control in partnership with Quality and Regulatory, maintaining a state of inspection readiness.

Manage the commercial manufacturing budget, capacity commitments and supplier performance, negotiating and governing agreements with external partners.

Partner cross-functionally with Regulatory, Quality, Commercial and Supply Planning to support launches, market expansions and lifecycle changes on time and in full.

Where You'll Work

This is a U.S.-based remote role that will require quarterly, or as needed visits to our San Francisco Office.

Who You Are

Historically the "Experience, Education, & Skills Requirement" section

(5-7 bullets max)

Bachelor's degree in packaging engineering, engineering, pharmaceutical sciences or a related field; 10+ years in commercial pharmaceutical manufacturing and supply.

Demonstrated packaging engineering background across primary and secondary drug-product packaging.

Hands-on ex-US commercial manufacturing and distribution experience, managing CMOs and partners across international markets.

Deep, practical expertise in artwork management, serialization / track-and-trace, and packaging & process validation.

Strong command of GMP, change control and regulatory expectations for commercial packaging across multiple geographies.

Experience launching a commercial product in the US and ex-US markets (EU, LATAM, Japan and others).

Familiarity with EU FMD, US DSCSA and comparable global serialization regulations.