Mami Zied

• Lead engineering and production activities in compliance with North American medical device regulations. • Act as primary liaison with Nissha engineering teams to ensure product specifications and quality requirements are met. • Oversee process validations (IQ, OQ, PQ) and ensure production readiness. • Train and mentor 5 technicians on validation procedures. • Implement performance tracking metrics (OEE, scrap rate) to drive process improvement.

• Managed the industrialization of new products and equipment from concept to production. • Standardized manufacturing methods and implemented continuous improvement initiatives. • Coordinated pre-series, prototypes, and PPAP documentation. • Deployed Lean 5S across production areas to improve workplace organization. • Collaborated with suppliers to integrate new production equipment. • Oversaw industrialization budgets and optimized operational costs.

• Led product launches and technical modifications across multiple production lines. • Optimized production flow including cutting, pre-assembly, overmolding, assembly, and packaging. • Managed prototype and spare part manufacturing areas. • Conducted root cause analysis of non-conformities and implemented corrective actions. • Standardized assembly procedures to ensure consistent quality. • Delivered staff training on updated manufacturing processes.