Jobs at New World Medical, Inc.

Lead and deliver new medical device R&D projects end-to-end, managing scope, schedule, budget, cross-functional stakeholders, and portfolio decisions. Mentor junior leads, drive consensus, ensure regulatory compliance (FDA/international), and improve development efficiency.

Lead quality engineering for medical device design assurance across product lifecycle. Provide independent oversight of design controls, risk management (ISO 14971), verification/validation, design transfer, supplier controls, and regulatory compliance (FDA QMSR, ISO 13485, EU MDR). Partner with cross-functional teams, review/approve V&V strategies and reports, apply statistical methods, support clinical and manufacturing readiness, resolve complex quality issues, and mentor quality engineers.

Lead planning, procurement, logistics, and inventory strategy to ensure consistent material availability, reduce shortages, improve supplier performance, implement MRP/SAP-based planning processes, and build repeatable warehouse and procurement systems. Manage and develop a team, drive inventory and supplier scorecards, mitigate supplier risk, and partner cross-functionally to align supply decisions with product development and production needs.

Lead and develop supplier quality engineering staff and programs for medical device suppliers. Oversee supplier selection, qualification, audits, CAPAs, PPAP, change control, risk management, KPIs, and cross-functional improvement efforts. Advise leadership on supplier performance, strategy, and compliance with medical device regulations.

The Senior Engineer will design and develop medical devices, manage product changes, perform testing, and ensure compliance with regulations while collaborating with team members and suppliers.

The Senior Principal Engineer designs and develops medical devices, overseeing all product development phases, managing resources, and mentoring junior engineers.