Benjamin Lewkowicz

Background

About Benjamin Lewkowicz

Biopharma MSAT & Program Management Specialist | Driving Operational Excellence, Process Optimization & Global Collaboration I am a bioprocess & operations professional with + of experience in GMP manufacturing environments across, and the, specialized in process optimization, Continued Process Verification (CPV), and operational excellence. My career spans technical and, where I deliver data-driven solutions that enhance efficiency, product quality, and compliance. Having worked with global teams and CMOs across three countries, I thrive at the intersection of technical expertise and project management—bridging science, operations, and strategy to streamline complex processes and achieve measurable results: GMP Manufacturing & Compliance – Deep knowledge of FDA/EMA standards, with hands-on experience in biologics and vaccine manufacturing. Process Optimization & CPV Leadership – Improved batch yield by +%, reduced lead times by %, and uncovered $ cost-saving opportunities through Lean, statistical analysis, and workflow standardization. Cross-Functional & International Collaboration – Coordinating teams across MS & T, Quality, Regulatory, Manufacturing, and CMOs to align strategy and deliver results. Project & Program Management – PMI-certified, experienced in leading global initiatives from supply chain optimization to lab efficiency projects.@ Leading CPV program, boosting yield and ensuring regulatory compliance. Standardized global shipment workflows, reducing lead times and strengthening CMO partnerships. 🧪 Drove Lean Six Sigma initiatives in MS & T labs, cutting turnaround time and costs. I’m passionate about advancing biotech & pharmaceutical manufacturing through innovation, efficiency, and cross-functional leadership. If you’re interested in discussing process optimization, operational strategy, or future trends in biopharma, let’s connect!