
Backed by extensive experience in manufacturing operations, I have built a proven track record of driving operational excellence, leading high-performing teams, and implementing continuous improvement initiatives that enhance productivity, quality, and overall business performance. My expertise in process optimization, workforce development, and strategic problem-solving has consistently improved operational efficiency, reduced waste, and delivered sustainable results.
Lead daily manufacturing operations within a high-volume production environment, driving safety, quality, delivery, productivity, and workforce development initiatives while supporting continuous improvement and operational excellence objectives.
Contributed to continuous improvement efforts by identifying opportunities for process enhancements and recommending appropriate solutions for sustainable implementation.
Mentored and coached direct reports through regular feedback and performance evaluations, leading to professional growth and skill development.
Medical Device Manufacturer & Testing Facility, ISO 13485 certified, and ISO 17025 accredited. Class 7 Cleanrooms compliant with ISO 14644/14698.
Routinely assessed team performance metrics to identify productivity gaps, implement corrective actions, and drive continuous improvement initiatives.
Drove operational performance by consistently meeting or exceeding KPI targets for on-time delivery, quality escapes, first-pass yield, and internal scrap reduction.
Promoted from Quality Engineer to Project Manager based on demonstrated technical expertise, customer leadership, and operational excellence. Directed cross-functional manufacturing programs supporting critical medical device components for a leading robotic surgical systems provider within an AS9100- and ISO 13485-certified precision machining environment.
Supported quality and compliance initiatives within an ISO 9001- and AS9100-certified plastics manufacturing environment by leading internal audits and Gemba walks, managing supplier corrective actions, facilitating MRB reviews, developing Zeiss Calypso CMM programs, and preparing FAIRs, PPAPs, and PFMEAs to ensure product conformity, strengthen regulatory compliance, and advance continuous improvement efforts.