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Designs, develops, prototypes, tests, verifies, and validates high-reliability medical devices and electromechanical assemblies. Responsibilities include manufacturing process development, tooling management, design documentation, risk assessments, regulatory submission support, production support, non-conformance resolution, and collaboration with electrical, software, manufacturing, and global design teams. The role also supports cost-effective, reliable, manufacturable designs and intellectual property development.

Design, prototype, test, and qualify mechanical enhancements for high-reliability medical devices. Investigate manufacturing and design failures, resolve production issues, evaluate nonconformances, develop manufacturing processes, review vendor validations, and create design verification test plans. Manage tooling, assess technical risks, maintain risk documentation, and ensure compliant engineering records while collaborating with electrical, software, manufacturing, and vendor teams.

Designs, prototypes, tests, and qualifies mechanical components for high-reliability medical devices. Investigates manufacturing and design failures, resolves production issues, evaluates non-conformances, develops manufacturing processes, reviews vendor validations, creates test plans, manages tooling, assesses risks, and maintains engineering documentation. Collaborates with electrical, software, design, and manufacturing teams to improve manufacturability, reliability, and cost effectiveness.

Supports sustaining medical device manufacturing and new product introduction on the swing shift. Troubleshoots hardware, system, process, and technical issues; improves yields, defects, scrap, and cycle time; maintains automated processes, tooling, fixtures, and test equipment; performs equipment and process validation; investigates failures and rejects; supports CAPA, preventive maintenance, documentation, and medical device quality system compliance.

Designs, prototypes, tests, and qualifies mechanical components for high-reliability medical devices. The engineer researches design options, develops manufacturing processes, manages tooling, supports product documentation and regulatory compliance, resolves production issues, evaluates nonconformances, and recommends design improvements. The role collaborates with global design and manufacturing teams while assisting senior engineers and supporting intellectual property development.

Leads cybersecurity engineering for connected medical devices across the product lifecycle. Responsibilities include security architecture, system threat modeling, regulatory requirement derivation, verification evidence, penetration testing, vulnerability assessment, remediation planning, interoperability security, and audit-ready documentation. The role coordinates with Systems, Software, Quality, and Regulatory teams while maintaining product security plans and supporting FDA, QMS, and medical device cybersecurity compliance.

Manage sales strategy and business development for Verathon’s GlideScope and BFlex airway products in the Netherlands. Build relationships with anesthesiologists, ICU and operating-room staff, generate new business, conduct product evaluations and presentations, prepare proposals, negotiate deals, forecast pipeline performance, meet revenue targets, and provide market and sales reporting.

Manage and improve electro-mechanical manufacturing processes, supporting production, quality, and product development teams. Responsibilities include process validation, tooling and test equipment design, automation, workflow optimization, failure investigations, CAPA activities, tolerance analysis, documentation, and design-for-manufacturing input. The role also supports new product introduction, prototype builds, quality-system compliance, and productivity improvements while applying Lean and Six Sigma principles.

Supports accounts payable and broader finance activities for Verathon’s EMEA entities. Responsibilities include processing invoices, coordinating banking activities, assisting with accruals, reconciliations, month-end close, statutory declarations, audits, controllership projects, process documentation, and management reporting. The role requires accurate, organized, independent work, strong communication, and collaboration across multicultural teams.

Leads a 6–10-person software engineering team developing applications for medical imaging devices. Oversees architecture, implementation, verification, validation, project delivery, agile processes, resource planning, and cross-functional collaboration. Mentors engineers, manages external development resources, and ensures compliance with medical-device standards. Defines software organization strategy, scales engineering capacity, and drives adoption of Generative AI to improve productivity, quality, innovation, and development efficiency.