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