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
As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.
For BridgeBio Full-Time U.S Based Roles
Financial & Rewards
Market-leading compensation
401(k) with employer match
Employee Stock Purchase Program (ESPP)
Pre-tax commuter benefits (transit and parking)
Referral bonus for hired candidates
Subsidized lunch and parking on in-office days
Health & Well-Being
100% employer-paid medical, dental, and vision premiums for you and your dependents
Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
Fertility & family-forming benefits
Expanded mental health support (therapy and coaching resources)
Hybrid work model with flexibility
Flexible, “take-what-you-need” paid time off and company-paid holidays
Comprehensive paid medical and parental leave to care for yourself and your family
Skill Development & Career Paths
People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
By applying, you acknowledge that BridgeBio will process your personal information as described in our Global Candidate Privacy Notice.
