Wade Law

Key Responsibilities: • Led and developed a team of 6 R&D Engineers, enhancing expertise in key competencies (DFSS, FEA/CFD, CAD, GD&T, 3DP). Managed team to led and support end-to-end product development and sustaining engineering across a diverse medical device portfolio (Infection Control Apparel, Fluid Management, Electromechanical Pump, Thermometry Devices), collaborated in all stages from feasibility and V&V to risk assessment, IP identification, and design transfer in alignment with PLM strategies. Responsible for team budget management and fostering global cross-functional collaboration with internal/external stakeholders and senior leadership. Key Achievements: • Maintained 100% positive Voice of Employee scores from direct reports for three consecutive years, reflecting excellence in leadership, career development support, empowerment, and team engagement. • Enabled team to launch 8 new private branded Chemogown 9200 series SKUs, delivering $1.7M in cost savings within 12 months of introduction. • Guided team collaboration leading to the successful Q3 2023 launch of the Kangaroo OMNI Enteral Feeding Pump in the US and Canada. • Spearheaded collaborative team efforts culminating in the successful Q4 2024 US launch of the Kendall SCD SmartFlow Compression System.

Key Responsibilities: • Led mechanical engineering for critical projects such as Negative Pressure Wound Therapy (NPWT) device CAD development and glove test method verification, ensuring technical rigor. Directed and mentored a team of 4 engineers (2 Senior, 2 CAD) on global initiatives, optimizing design workflows for timely solutions. Concurrently, advanced the team's technical capabilities by developing and implementing targeted training in advanced simulation and freeform CAD modeling, while driving mechanical design innovation and contributing expert solutions to complex engineering challenges within product development lifecycles. Key Achievements: • Patented Innovation: Secured two US Non-Provisional Patents as a key inventor for novel fluid management suction canister systems, demonstrating significant technical innovation: o US Patent 10,765,854: "PORT CONNECTOR FOR MEDICAL WASTE FLUID RECEPTACLES AND METHODS OF USE" o US Patent 10,814,047: "FLUID COLLECTION SYSTEMS AND METHODS OF USE"

Key Responsibilities: • Led technical strategy and execution for developing next-generation Fluid Management systems, pump technologies, and private-label products, ensuring market relevance and technical feasibility. Directed rigorous Verification & Validation (V&V) programs to guarantee product safety, efficacy, and compliance with user requirements and global regulatory standards. Additionally, managed the technical aspects of product design transfer to manufacturing partners, including successful IQ/OQ/PQ completion for scalable production. To cultivate future innovation, proactively built and managed external research partnerships for technology scouting. Championed Design for Excellence (DFX), advancing the team's simulation (FEA/CFD) and modeling proficiency to accelerate development cycles and create more robust designs. Key Achievements: • Enhanced OR Efficiency: Successfully developed the 4-UP OR Tubeless Vacuum Suction Canister System, demonstrably reducing operating room turnover time and improving usability based on international user studies (USA, EU, APAC).

Key Responsibilities: • Led the end-to-end design, testing, and verification for diverse medical disposables (Surgical Tapes, Bandages, Wound Care, Anesthesia Masks, LMA, ETT) including CAD development and designing custom test equipment per industry standards to support successful commercialization. Concurrently served as the primary designer for Fluid Management and Irrigation Pump Systems, driving these projects from concept to design freeze by championing FEA/CFD simulations and Proof of Concept (POC) testing for comprehensive design validation (form, fit, function).

Key Responsibilities: • Led design/development of next-generation percutaneous technologies (PAD); co-led strategic development, expansion, lifecycle management for Chocolate™ PTA balloon catheter product line, overseeing critical project milestones. Managed comprehensive DVT, OQ, PQ documentation/execution, ensuring product compliance (esp. Chocolate™ PTA). Directed successful design transfer to local contract manufacturers, providing in-depth training for teams. Collaborated extensively with Manufacturing, Quality, Regulatory for manufacturability, quality, safety, efficacy throughout lifecycle. Established/qualified (IQ) new R&D laboratory, managing equipment setup/calibration for operational readiness/data integrity. Managed key vendor relationships (local/overseas) for effective communication/reliable supply chains. Key Achievement: • Pioneered Market Access for Chocolate™ PTA: Co-led the core engineering effort for the Chocolate™ PTA balloon catheter family, achieving successful product launch marked by critical regulatory approvals: CE Mark (Jan 2011) and landmark FDA clearance (Dec 2011) – the first Singapore-developed medical device to gain FDA approval.

Key Responsibilities: • Designed and developed innovative interventional cardiology devices, including drug-eluting coronary stents and balloon catheter systems, focused on enhancing patient care outcomes. Drove the development and expansion of the BioMatrix Flex™ PTCA balloon catheter line through rigorous DVT, OQ/PQ, risk management, and stability testing. Led development projects for medical tubing extrusion and medical balloon forming, implementing laser bonding technology to significantly improve manufacturing processes. Provided technical leadership and training to manufacturing personnel (local/overseas) on critical processes (resin conditioning, extruder operation, laser bonding). Designed and managed vendor fabrication of custom testing tools/fixtures for accurate in-house R&D validation activities. Partnered effectively with Manufacturing, Quality Assurance, and Regulatory Affairs teams to ensure product manufacturability, quality, safety, efficacy, and compliance throughout the development lifecycle. Key Achievements: • Product Launch & Regulatory Success: Played an integral role in the successful development and launch of the BioMatrix Flex™ Drug-Eluting PTCA balloon catheter product family, securing CE Mark approval (January 2010). • Product Line Extension: Led the BioMatrix Flex™ stent length extension project (33mm, 36mm) from concept through development, resulting in successful CE Mark approval and product launch (September 2010), expanding market reach. • Technical Marketing & KOL Engagement: Successfully presented and demonstrated enhanced trackability features of the BioMatrix Flex™ system to clinicians at major international cardiology conferences (TCT 2010, Washington D.C.; EuroPCR 2010, Paris).

Key Responsibilities: • Led a dedicated project team within the Automotive division, overseeing the complete lifecycle of automotive electrical connector design and development, from initial conceptualization through to successful commercialization. Executed rigorous hands-on design engineering and comprehensive evaluations, encompassing plastic material assessments, simulation studies (FEA), prototype sample testing (component/assembly), Failure Mode Effects Analysis (FMEA), iterative CAD design (SolidWorks), and safety factor analysis to ensure robust, reliable connector performance meeting stringent structural and environmental standards. Fostered effective international collaboration with R&D counterparts on joint project initiatives, promoting global knowledge sharing and standardized practices, and managed relationships with critical component vendors, ensuring timely delivery and quality compliance for meeting project milestones. Developed and conducted targeted SolidWorks CAD software training for junior design engineers, enhancing their technical proficiency and contributing to team capability development. Key Achievements: • Co-designed and successfully launch the pioneering 80P airbag connector, a critical factor in securing a major tender from Hyundai Autonet which significantly established the company's presence in the Korean automotive industry (2005-2006). • Co-led the strategic development and expansion of the 80P airbag connector series, resulting in key tender awards from Beijing Jinheng Automotive Safety Technology Holdings Ltd and enabling the company's successful entry into the competitive Chinese automotive market (2006-2007).