Venessa Galate

About Venessa Galate

With over 25 years of dynamic experience across the Consumer, Pharmaceuticals, and Medical Devices sectors, I am a highly motivated leader with a proven track record in Quality and Compliance, Inspection Readiness, Customer Service Strategies, Operations Improvement, and Supply Chain System Development, Deployment, and Product Lifecycle Management. At present, I hold the leadership role in the Supply Chain Standards, Systems, and Solutions Center of Excellence at Johnson & Johnson, where I wholeheartedly dedicate myself to delivering exceptional customer value through the innovative design, deployment, and lifecycle management of end-to-end supply chain solutions.I drive transformative change initiatives and champion operational excellence throughout Johnson & Johnson, leading a high performing team. My unwavering commitment to excellence is evident in my strategic planning, execution, and relentless pursuit of continuous improvement. I harness my expertise in Quality, Lean Six Sigma, process optimization, system architecture, and system design to drive efficiencies and elevate the customer experience while maintaining the highest standards of quality and compliance. I am a proactive leader who nurtures a culture of innovation and continuous improvement, consistently empowering my team to not only meet but exceed expectations, ultimately bringing about positive change.

Experience

1. VP Supply Chain Excellence

   Johnson & Johnson

   Mar 2025 — Present · New Brunswick, NJ, US

   As the VP of supply chain excellence at Johnson and Johnson I lead our team in the Operating System program focusing on driving operating efficiencies, continuous improvement and company growth. We emphasize mentoring future talent and leveraging external benchmarks to enhance the customer experience and sustain operational excellence.

Education

• Executive MBA

  In Progress, Business Law

• Fairleigh Dickinson University

  Bachelor of Science (B.S.), International Business

  1999 — 2003

• Berkeley College-New York

  International Business

  1996 — 1998

Skills

• Pharmaceutical Industry
• Clinical Trials
• Gcp
• Ctms
• Quality Assurance
• Oncology
• Change Management
• CRO
• Fda
• Edc
• Clinical Development
• Clinical Research
• Biotechnology
• Gxp
• Pharmacovigilance
• Ich-Gcp
• 21 Cfr Part 11
• Therapeutic Areas
• Regulatory Affairs
• Sop
• Computer System Validation
• Process Improvement
• Validation
• Corrective and Preventive Action (Capa)
• Regulatory Submissions
• Drug Development