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Process payroll for indirect labour: verify timekeeping, calculate wages and deductions, maintain leave records, resolve payroll inquiries, prepare management reports, ensure compliance, and collaborate with HR and finance. Familiarity with payroll systems (Infotech HRMS) and Microsoft Office expected.
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Lead implementation and maintenance of the quality system for the Malaysia facility, oversee inspection/testing and nonconformance control, implement SPC and quality metrics, manage quality improvement projects, coordinate with corporate on acceptance procedures, ensure calibration of inspection equipment, and hire/lead the quality team including training and employee relations.
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Plan, conduct, document, and report internal QMS audits to ensure compliance with medical device and pharma regulations (ISO 13485, 21 CFR 820, EU MDR). Prepare audit plans and reports, verify CAPA effectiveness, support customer/certification/regulatory audits, maintain records, collaborate with cross-functional teams, and drive continuous improvement of the Quality Management System.
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The Assistant Engineer, Quality ensures product quality across the lifecycle, supports inspections, monitors performance, maintains QMS, and collaborates across teams for improvements.
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The Manufacturing Supervisor oversees daily operations and personnel in manufacturing, ensuring compliance with quality regulations, training staff, and meeting production goals.
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Process and pay vendor invoices; research and resolve PO/variance/receiving issues; reconcile vendor accounts, prepayments, and returns; ensure approvals and internal controls; support month-end close, journal entries, and AP batch reviews; provide customer service and complete special projects.
Healthtech
Lead global indirect procurement strategy across facilities, IT, MRO, CAPEX and services. Drive category strategies, spend analysis, supplier governance, contract negotiations, Coupa P2P controls, supplier diversity, risk mitigation, VSM/Kaizen process improvements, and cross-functional sourcing to realize cost synergies and operational resiliency.
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The Supplier Quality Engineer ensures compliance with quality requirements, manages supplier selection and monitoring, conducts audits, and develops quality metrics while collaborating with suppliers and engineering teams.
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Serve as clinical expert on Masimo non-invasive monitoring products, educate and train hospital customers, lead clinical evaluations and deployments, support sales and market penetration, present product demonstrations and competitive positioning across hospital units.
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Provide clinical support and field implementation for non-invasive patient monitoring across a regional territory. Develop customer solutions with sales, train clinical and nursing staff, present products at events, document customer feedback in CRM, collaborate with service and marketing teams, and travel ~60% for on-site support.
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The Engineer II develops, tests, and supports cloud-based and web-enabled software solutions, ensuring reliability and compliance in a regulated environment.
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The Senior Accountant manages general ledger accounting, prepares financial reports, supervises the accounting close process, and ensures compliance with policies. They support audits, handle budgets, and manage fixed assets while collaborating with various teams and adapting to business changes.
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The Sr Business Systems Analyst will support Oracle E-Business Suite projects for Finance, working with users to identify requirements, implement solutions, and improve processes.
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The Principal Engineer leads the development of ECG signal processing algorithms for accurate cardiac monitoring and collaborates with cross-functional teams for regulatory-compliant solutions.
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Sell Masimo acute-care products to hospitals, build clinical relationships, conduct demos and evaluations, drive capital and sensor sales, maintain CRM forecasts, coordinate clinical evaluations and team selling, present value propositions, and travel overnight as required.
Healthtech
Design and document complex multilayer PCB/PWB layouts for new product development and sustaining engineering. Optimize for electrical performance, manufacturability, reliability, cost, and quality. Support prototypes, verification, production transfers, DFM/DFA/DFT and IPC standards. Partner cross-functionally and drive continuous improvement, CAD standards, and supplier collaboration.
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Lead international and domestic regulatory registrations and submissions for medical devices. Draft 510(k)s, maintain technical documentation, manage filings and regulatory databases, coordinate with regional teams, train staff on requirements, support QA/Engineering, and respond to health authority inquiries to ensure compliance with FDA and international regulations.
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Lead PMO operational excellence for engineering portfolios by developing governance, portfolio management, reporting, and tooling. Build executive dashboards (Power BI), manage intake, prioritization, capacity planning, and portfolio reviews, coach Project Managers, and drive cross-functional alignment across Engineering, Product, Quality, Regulatory, Clinical, and Operations.
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The Clinical Sales Representative is responsible for selling Masimo products in a competitive market, engaging with hospital staff, and executing sales strategies to convert accounts, while managing forecasts and providing market insights.
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Lead and execute Computer System Validation (IQ/OQ/PQ) for GxP-regulated systems (ERP, QMS, MES, cloud/SaaS), ensuring compliance with 21 CFR Part 11/820, ISO 13485, GAMP5. Collaborate cross-functionally, produce validation documentation, manage change control, support audits/inspections, and maintain data integrity aligned with ALCOA+.



