Commercialization Project Manager

About BridgeBio

BridgeBio is a biopharmaceutical company dedicated to discovering, developing, and delivering transformative medicines for patients living with genetic diseases and genetically defined cancers. Since our founding in 2015, we have built a diverse portfolio of more than 20 drug development programs, ranging from early discovery to late-stage clinical trials, across multiple therapeutic areas including precision oncology, cardiology, endocrinology, neurology, and renal disease. We have already achieved regulatory approval for three therapies and continue to advance promising science from academia into meaningful treatments for patients worldwide.

Who We Are

BridgeBio is a global biotechnology company with our Global Headquarters located in San Francisco, USA, and our International HQ located in Zug, Switzerland. Since establishing our European presence in 2021, we’ve been building empowered, high-performing teams across countries — experienced colleagues who move quickly, take ownership, and are fueling the company’s international growth.

At BridgeBio, you’ll find an energetic and collaborative culture where pragmatism meets bold decision-making. We embrace uncertainty with confidence, guided by our commitment to making a meaningful impact for patients. Our people are trusted and empowered, united by urgency, purpose, and the drive to advance science for patients around the world.

What You’ll Do

The Commercialization Project Manager will report directly to the Head of International Supply Chain and will work remotely from the Netherlands. This role is responsible for driving the successful execution of product commercialization activities within Supply Chain. This role acts as the primary link between the Packaging and Regulatory departments, ensuring flawless execution of Artwork milestones to support a timely product launch. In addition, this role will own the Supply Chain Change Control strategy, support the implementation of a Product Variation Management process, and provide flexible project support across the broader Supply Chain portfolio.

Responsibilities:

Change Control Management

Initiate, assess, and manage change controls related to commercialization activities

Coordinate cross-functional impact assessments with Quality, Regulatory, Manufacturing, Packaging/Artwork and other teams as required

Track change control progress against timelines, escalating risks and delays proactively

Ensure change controls are documented in compliance with Good Documentation Practices and other GxP requirements

Variation Management

Support the creation and continuous improvement of the product Variation Management process

Coordinate post-approval variations related to product changes (CMC / Labeling) and aligns with internal stakeholders on the approval and implementation windows

Maintain variation trackers and ensure traceability between variations, change controls, manufacturing and artwork updates

Ensure Regulatory approval, Change Control and artwork development timelines are synchronized between the departments

Other Responsibilities

Support other commercialization projects as needed, including new product launches, site transfers, packaging changes, and Supply Chain network changes

Develop and maintain Commercial Supply Chain project plans, timelines and risk logs

Facilitate cross-functional project meetings and drive actions to closure

Provide status reporting to Supply Chain Leadership and other stakeholders

Other duties as assigned

Where You’ll Work

This is a remote role based in the Netherlands, with approximately 5% travel anticipated.

Who You Are

Bachelor’s degree in a related field, such as Life Sciences, Supply Chain, Logistics, Project Management or Business Administration

Minimum of 10 years of Supply Chain / Project Management experience, including Life Sciences industry experience with commercial products

Demonstrated experience with Change and variation management processes in a regulated environment

Experience working across multiple markets/jurisdictions (EU, LACAN, MENA & APAC) is a must

Experience supporting product launches & Life Cycle Management activities

Experience coordinating artwork/labeling processes and understanding of regulatory submission cycles is strongly preferred

Strong and clear understanding of GMP/GDP requirements and pharmaceutical industry best quality practices

Familiarity with quality management systems (QMS) and regulatory information management systems

Proficiency in project management tools (e.g., Smartsheet, MS Project)

Fluent in written and spoken English

Strong cross-functional communication and stakeholder management skills

Excellent analytical and problem-solving skills, with strong attention to detail

Strong organizational skills with ability to manage multiple concurrent projects and timelines