Commercialization Project Manager

This is a fully remote position, open to applicants in Netherlands.

📋 Description

• Lead the effective implementation of product commercialization initiatives within the Supply Chain.

• Serve as the primary liaison between the Packaging and Regulatory departments to guarantee seamless execution of Artwork milestones, facilitating timely product launches.

• Take ownership of the Supply Chain Change Control strategy.

• Assist in the execution and ongoing enhancement of the product Variation Management process.

• Initiate, evaluate, and oversee change controls associated with commercialization efforts.

• Organize cross-functional impact assessments involving Quality, Regulatory, Manufacturing, Packaging/Artwork, and additional teams.

• Monitor the progress of change controls against established timelines and proactively highlight risks and delays.

• Ensure that change controls adhere to Good Documentation Practices and other GxP standards.

• Coordinate post-approval product variations pertaining to CMC and Labeling modifications.

• Maintain variation trackers and ensure traceability among variations, change controls, manufacturing, and artwork updates.

• Align Regulatory approval, Change Control, and artwork development timelines.

• Support commercialization projects, including new product introductions, site transfers, packaging modifications, and Supply Chain network adjustments.

• Create and manage project plans, timelines, and risk logs for Commercial Supply Chain initiatives.

• Facilitate cross-functional project meetings and drive actions to completion.

• Provide status updates to Supply Chain Leadership and other stakeholders.

• Execute additional responsibilities as assigned.

⛳️ Requirements

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

• At least 10 years of experience in Supply Chain / Project Management, specifically within the Life Sciences sector involving commercial products.

• Proven experience with Change and variation management processes in a regulated environment.

• Experience across multiple markets/jurisdictions (EU, LACAN, MENA & APAC) is essential.

• Background in supporting product launches and Life Cycle Management activities.

• Strongly preferred experience in coordinating artwork/labeling processes and an understanding of regulatory submission cycles.

• Comprehensive understanding of GMP/GDP requirements and best quality practices in the pharmaceutical industry.

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

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

• Fluency in written and spoken English.

• Robust cross-functional communication and stakeholder management abilities.

• Exceptional analytical and problem-solving skills, with a keen attention to detail.

• Strong organizational skills with the capacity to manage multiple concurrent projects and timelines.

🏝️ Benefits

• Competitive compensation package.

• Referral bonuses for successfully hired candidates.

• Fertility and family-forming benefits.

• Enhanced mental health support, including therapy and coaching resources.

• Flexible paid time off policy, allowing employees to take what they need, along with company-paid holidays.

• Comprehensive paid medical and parental leave.

• Opportunities for skill development and internal mobility.

• Career advancement through regular feedback, continuous education, and professional development programs via LinkedIn Learning, LifeLabs, and BetterUp Coaching.

• Financial incentives, recognition from peers, and opportunities for growth.