Shape and communicate a compelling vision for advanced therapies manufacturing.
Influence and inspire cross-functional, multidisciplinary teams in an international environment.
Lead the implementation of smart manufacturing technologies & automation and data-driven process monitoring.
Develop and execute a robust data and digital strategy for process verification and lifecycle management.
Accountability for technology transfer, process qualification, and comparability for advanced therapy products.
Ensure compliance with global regulatory requirements (FDA, EMA, etc.), authoring and reviewing technical reports and regulatory submissions.
Shape facility design for manufacturability, automation, and lean operations.
Recruit, retain, and develop a diverse, world-class team of technical leaders, scientists, and engineers.
Champion business cases for technology implementation and strategic projects.
Requirements
University/Bachelor’s Degree in Science/Engineering or equivalent with 15+ years in Biotech/Pharmaceutical, or Master’s/PhD with 10+ years relevant experience.
Proven leadership in new facility design, construction, and operational readiness for advanced therapies or innovative product technologies.
Deep expertise in automation systems, data integration, and digital transformation in biopharma manufacturing.
Hands-on experience in manufacturing operations and/or R&D for cell/gene therapy products, vaccines, or other advanced therapies.
Demonstrated success in technology transfer, process qualification, and regulatory submissions for global markets.
Advanced knowledge of cGMP compliance, change management, and validation requirements.
Strong data analytics/statistics skills and deep experience with lean/operational excellence tools.
Exceptional judgment, prioritization, and decision-making abilities in fast-paced environments.
Effective communicator and influencer across all levels of the organization.
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