Top Tech Jobs & Startup Jobs

Provide engineering support for medical device product transfers, including technical planning, equipment analysis, validation documentation, process qualification, PFMEA, control plans, and PPAP. Ensure compliance with Stryker procedures, GMP, safety, quality, and regulatory requirements. Collaborate with quality and multidisciplinary teams, review engineering outputs, solve manufacturing and design problems, and coach other engineers.

Design and optimize CNC machining processes for precision medical device components from prototype through mass production. Responsibilities include DFM reviews, process planning, tooling and fixture development, CAM programming, machining simulation, trial production validation, process documentation, IQ/OQ/PQ and process validation, quality analysis, and production ramp-up. The role requires collaboration with R&D, quality, production, and purchasing teams while maintaining ISO 13485 and GMP compliance.

Designs and optimizes CNC machining processes for precision medical device components from prototype through mass production. Responsibilities include DFM reviews, CAM programming, tooling and fixture development, process validation, SOP creation, troubleshooting machining defects, and compliance with ISO 13485 and GMP. Collaborates with R&D, quality, production, and purchasing teams to improve yield, cycle time, cost, and production stability.

Leads systems engineering for robotic surgical end effectors and electromechanical subsystems. Translates clinical and user needs into requirements, architectures, interfaces, and verification strategies. Coordinates integration across electrical, mechanical, software, controls, clinical, quality, and regulatory teams. Supports risk management, design history file documentation, system verification and validation, technical trade studies, and process improvements while mentoring engineers.

Owns supply planning for a product portfolio across ANZ, translating demand forecasts into replenishment and inventory plans. The role manages supply risks, stock availability, excess and slow-moving inventory, and contributes to S&OP/IBP processes. It requires collaboration with Demand Planning, Sales, Operations, Customer Service, and global teams, along with continuous improvement of planning systems and processes.

Leads a multidisciplinary robotics engineering organization responsible for medical technology platform development. Oversees people management, staffing, contractors, engineering execution, resource planning, budgets, schedules, risks, and cross-functional delivery. Partners with project and technical leaders to translate program priorities into engineering plans while ensuring compliance with design controls, risk management, quality systems, and regulatory requirements. Supports distributed teams and periodic travel between development sites.

Supports New Product Development teams and the Project Management Office through governance and portfolio execution. Responsibilities include data entry, metrics tracking, resource analysis, portfolio trend reporting, and improving project tools, workflows, and execution speed. The intern collaborates with program, project, and portfolio managers, documents complex processes, presents findings, and gains experience in a medical technology environment.

Supports supply chain operations, material planning, procurement visibility, inventory control, logistics, warehouse activities, and end-to-end material flow tracking. Analyzes process gaps and root causes, recommends improvements, documents complex processes, and presents findings. Collaborates with internal stakeholders across production scheduling, receiving, distribution, kitting, and shipping while developing professional and operational skills.

Manages production control and supply planning activities, including master scheduling, production planning, shop floor scheduling, dispatching, and material requirements planning. Oversees inventory, WIP, material and labor performance, production schedules, and resource planning to support on-time delivery and operational efficiency. Leads process improvement, reporting, ERP-based planning, cross-functional collaboration, and development of production planning personnel.

Leads systems engineering for complex medical device products, including system architecture, technical strategy, requirements development, traceability, verification planning, integration, risk assessment, and design decisions. Translates customer, clinical, and business needs into system requirements while coordinating software, electrical, mechanical, quality, regulatory, and clinical stakeholders. Guides multidisciplinary product development from concept through verification, ensures compliance with design controls, evaluates emerging technologies, and influences global teams without direct authority.