Top Tech Jobs & Startup Jobs

Own, implement, validate, secure, and continuously improve manufacturing applications supporting medical device production. Lead computer system validation, lifecycle management, change control, data integrity, user access, and regulatory compliance. Support SAP Business One manufacturing processes, develop SQL queries and reporting solutions, and partner with Quality, Regulatory, Supply Chain, IT, Engineering, and vendors. The role also supports business continuity, system performance, process improvement, and delivery of business-critical projects.

Supports Stryker’s intercompany finance team by verifying and entering invoices into ERP systems, preparing posting documentation, performing balance sheet reconciliations, clearing invoices with payments, and assisting with month-end closing activities.

Designs and optimizes CNC machining processes for medical device components from prototype through mass production. Responsibilities include DFM reviews, process planning, tooling and fixture development, CAM programming, machining validation, trial production, technical documentation, and troubleshooting. Collaborates with R&D, quality, production, and purchasing teams to improve yield, cost, cycle time, and process stability while complying with ISO 13485 and GMP requirements.

Manufacturing Engineer responsible for CNC process design, DFM reviews, CAM programming, tooling and fixture development, machining simulations, prototype validation, process documentation, and production transfer. The role resolves machining defects, optimizes yield and cycle time, supports IQ/OQ/PQ and process validation, maintains ISO 13485 and GMP compliance, and collaborates with R&D, quality, production, and purchasing teams on medical device component manufacturing.

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.