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Develop and maintain automated test frameworks, author and execute manual and automated test protocols, analyze results, review requirements and code, investigate defects, and improve testing processes for regulated medical device software.

Develops, qualifies, and releases electronic components for medical device products. Creates component specifications and drawings, drives supplier quality and reliability, leads failure analysis and corrective actions, evaluates suppliers and alternate sources, defines receiving inspection requirements, and collaborates with engineering, manufacturing, quality, and program teams throughout new product development.

Leads automation engineering for a regulated medical-device manufacturing site. Responsibilities include developing automation roadmaps, supporting and troubleshooting automated equipment, leading machine vision and robotics initiatives, qualifying and validating equipment, implementing corrective actions, improving reliability, and deploying emerging technologies. Partners with cross-functional and regional teams to execute automation projects and ensure compliance with quality, safety, validation, and regulatory requirements. The role is onsite in Danvers, Massachusetts, with 10–15% travel.

Designs, develops, validates, and supports digital manufacturing architectures connecting plant-floor equipment, PLCs, databases, MES, ERP, and enterprise systems. Builds Ignition applications, HMIs, dashboards, SQL databases, reports, alarms, historian systems, and KPI monitoring tools. Troubleshoots connectivity issues, supports equipment launches, integrates OPC-UA communications, collaborates on secure OT/IT architectures, and documents system changes.

Provides legal and compliance guidance on global import and customs matters, including country of origin, valuation, tariff classification, trade remedies, FTAs, CTPAT, customs inquiries, investigations, audits, and regulatory changes. Partners with legal, supply chain, compliance, and business teams to mitigate global trade risks, develop controls and standards, support due diligence and litigation, and deliver employee training.

Designs, develops, implements, and improves learning solutions supporting operational processes, workforce capability, system adoption, and business performance. Conducts needs analyses, creates curricula and digital learning content, manages complex learning projects, facilitates workshops and train-the-trainer programs, evaluates learning effectiveness, and partners with stakeholders to ensure quality, compliance, accessibility, and governance. Provides coaching and guidance to trainers, subject matter experts, project teams, and external partners across multiple countries and functions.

Develops and validates automated software and systems testing for regulated medical products. Responsibilities include creating test strategies, traceability matrices, test architectures, automated testing components, CI/CD execution, debugging, performance analysis, and product verification. Collaborates across global teams, supports product development activities, troubleshoots existing products, and communicates technical findings. The role applies AI coding tools, agentic automation, and modern Agile, TDD, and BDD practices.

Designs and executes manual and automated testing for web applications, APIs, and cloud software. Develops test automation frameworks, performs functional and integration testing, creates verification and validation documentation, investigates defects, supports regulatory requirements, and improves testing processes. Collaborates with development, systems engineering, and quality teams throughout the software development lifecycle.

Tests medical device software systems and applications by developing and executing test plans, scripts, and automation. Documents results for regulatory submissions, verifies technical and functional requirements, analyzes workflows, and recommends quality improvements. Collaborates with developers to resolve defects and improve product configurations. The role also reviews testing methodologies and supports software-controlled hardware testing in a regulated medical device environment.

Supports Medtronic’s global property and casualty insurance programs by preparing and validating insurance data, reviewing policies and contracts, administering certificates, supporting workers’ compensation reporting, maintaining records and SharePoint content, responding to insurance inquiries, and assisting with merger and acquisition due diligence and integration.