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Manages and grows strategic private-sector healthcare accounts across the UK for a medical device portfolio. Responsibilities include executive relationship management, strategic account planning, consultative selling, pricing and contract negotiations, business reviews, financial modeling, value proposition development, and cross-divisional coordination. The role supports customer purchasing processes, resolves supply chain and contracting issues, monitors account performance, and collaborates with sales, finance, market access, and healthcare economics teams. Field-based work involves 50% travel.

Provide technical pre- and post-sale customer support, manage service contracts, coordinate cross-functionally to resolve RMAs, scheduling, shipping, and invoicing issues, identify upsell opportunities, and maintain strong customer relationships to support service and product revenue.

Leads manual and automated software testing for complex medical-device software systems. Responsibilities include test strategy, planning, risk analysis, test platform development, documentation, quality-system compliance, resource and schedule management, cross-functional collaboration, technical issue resolution, process improvement, and mentoring engineers across the software lifecycle.

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.