Commercialization Project Manager
Posted 15hrs ago
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Job Description
Commercialization Project Manager advancing rare-disease medicines at BridgeBio Pharma. Driving change control, product variations, artwork milestones, and Supply Chain launches from the Netherlands.
Responsibilities:
- Drive the successful execution of product commercialization activities within Supply Chain
- Act as the primary link between Packaging and Regulatory departments to ensure flawless execution of Artwork milestones supporting timely product launches
- Own the Supply Chain Change Control strategy
- Support implementation and continuous improvement of the product Variation Management process
- Initiate, assess, and manage change controls related to commercialization activities
- Coordinate cross-functional impact assessments with Quality, Regulatory, Manufacturing, Packaging/Artwork, and other teams
- Track change control progress against timelines and proactively escalate risks and delays
- Ensure change controls comply with Good Documentation Practices and other GxP requirements
- Coordinate post-approval product variations related to CMC and Labeling changes
- Maintain variation trackers and traceability between variations, change controls, manufacturing, and artwork updates
- Synchronize Regulatory approval, Change Control, and artwork development timelines
- Support commercialization projects 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
- Perform other duties as assigned
Requirements:
- 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
Benefits:
- Market-leading compensation
- Referral bonus for hired candidates
- Fertility & family-forming benefits
- Expanded mental health support (therapy and coaching resources)
- Flexible, “take-what-you-need” paid time off and company-paid holidays
- Comprehensive paid medical and parental leave
- Opportunities for skill development and internal mobility
- Career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
- Financial rewards, peer-to-peer recognition, and growth opportunities



















