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Designs, validates, troubleshoots, and improves manufacturing processes for medical devices. Develops equipment, tooling, fixtures, tests, and process alternatives; analyzes data; supports product development, sustaining engineering, risk management, and design controls. Collaborates with production, quality, suppliers, and cross-functional teams to resolve manufacturing issues, manage engineering projects, train operators, and ensure product safety, quality, compliance, and delivery.

Leads strategic sourcing for new product development and introduction programs, selecting and managing suppliers, negotiating contracts, mitigating supply risk, optimizing costs, and supporting product commercialization. Partners with Engineering, Operations, Quality, Finance, Marketing, and suppliers to achieve launch milestones, margin expansion, supply continuity, and long-term growth.

Leads a multi-site manufacturing engineering organization supporting growth, product development, and product transfers. Builds and mentors engineering teams, aligns projects and resources with business priorities, ensures regulatory and process compliance, resolves cross-functional production issues, and drives Lean, 5S, innovation, and operational excellence. Develops long-term strategic roadmaps, manages budgets and capital investments, and identifies process improvement and cost-saving opportunities in regulated medical device manufacturing.

Supports capital equipment contracting and commercial processes by preparing and coordinating agreements, reviewing terms and documentation, identifying risks, managing approvals and execution, maintaining contract records, and serving as a contract-related point of contact. Conducts pricing analysis and evaluates promotions and rebates while improving contracting workflows, intake processes, system handoffs, and reporting.

Leads financial compliance for the Medical Division, overseeing technical accounting, US GAAP, SOX controls, audits, financial policies, reporting, and complex transactions. Partners with corporate and divisional stakeholders to assess risks, resolve control deficiencies, implement accounting guidance, standardize processes, and improve reporting accuracy. Manages quarter-end compliance and documentation while developing the financial compliance team and supporting strategic business initiatives.

Owns electrical hardware design and development for complex neurosurgical medical device consoles. Responsibilities include designing electrical components and subsystems, prototyping, bench testing, circuit analysis, troubleshooting, engineering research, requirements translation, regulatory-oriented testing, design documentation, risk management, and collaboration with multidisciplinary R&D, quality, manufacturing, regulatory, clinical, marketing, and project management teams.

Provides field-based operating room and sterile processing support for Stryker and third-party surgical equipment. Responsibilities include equipment setup, readiness checks, intraoperative adjustments, troubleshooting, post-procedure breakdown, cleaning, consumable restocking, documentation, staff education, instrumentation reprocessing, and repair coordination. The role supports minimally invasive procedures, works closely with clinical and SPD teams, follows safety and privacy standards, and provides rotating, on-call, weekend, overnight, and regional coverage.

Supports implementation and administration of Stryker’s Vocera healthcare communication solution onsite. Responsibilities include managing databases, servers, devices, inventory, backups, updates, troubleshooting, documentation, end-user support, clinical workflow assistance, and training nurses and clinicians. The specialist also collaborates with customer support teams, maintains issue records, and administers user satisfaction programs.

Supports Stryker’s global privacy compliance program by managing regulatory inquiries, filings, privacy impact assessments, individual rights requests, audits, monitoring, metrics, and process improvements. Partners with legal, compliance, IT security, regulators, and business stakeholders to assess privacy risks, maintain compliance, track requests, and escalate issues appropriately.

Leads data architecture and management for a robotic medical device platform. Defines data logging, interfaces, requirements, models, governance, security, interoperability, and lifecycle strategies across clinical and engineering domains. Drives cross-functional architecture, systems integration, verification, validation, risk analysis, and regulatory compliance. Mentors engineers and supports product development and technology strategy.