Jobs at Masimo

Educates customers and clinical users on Masimo pulse oximetry and patient-monitoring solutions. Conducts clinical evaluations, supports research accounts, trains distributors and end users, presents product value, and partners with sales teams on key-account conversion and market-development programs. Maintains clinical and product expertise, monitors relevant research, supports competitive positioning, and communicates product and regulatory needs. The role covers Madrid, Castilla-La Mancha, and Castilla y León, with extensive travel.

Supports international financial reporting and compliance for subsidiaries, including standalone financial statements, audits, tax payments and filings, monthly close activities, reconciliations, technical accounting, and consolidation. The role also assists the Accounting Manager with analyses and related activities. This is a 12-month temporary contract requiring fluency in French and English.

Processes full-cycle accounts payable for assigned vendors, including invoice coding, approval routing, purchase order matching, discrepancy resolution, vendor account reconciliation, debit processing, and employee expense report auditing. Maintains filing systems, supports special projects, and collaborates with purchasing teams, requisitioners, vendors, and management. Requires accuracy, knowledge of accounting principles, research and problem-solving skills, strong communication, and proficiency with ERP, spend management, travel software, Excel, and Office tools.

Sell Masimo medical devices, monitoring technologies, and OEM solutions across Catalonia and the Balearic Islands. Develop hospital accounts, demonstrate products, negotiate with physicians and administrators, participate in tenders, partner with distributors, forecast sales, track market activity, and manage territory expenses. The role requires strong medical device sales experience, clinical knowledge, multilingual communication, and frequent travel.

Ensures compliance with national and international trade regulations, including import/export laws, sanctions, customs requirements, tariff classification, and documentation. Conducts risk assessments, audits, and monitoring; maintains trade records; develops corrective actions and process improvements; trains employees; and collaborates with logistics, finance, legal, sales, customs authorities, and government agencies.

Coordinates and improves molding processes in a regulated manufacturing environment. Provides engineering support for automation, troubleshooting, calibration, validation, equipment maintenance, and process improvements. Investigates equipment and quality failures, develops permanent corrective solutions, manages change requests and validation documentation, and designs engineering studies and technical specifications. Coaches technicians, supports cost reduction and equipment efficiency, maintains compliance with OSHA, ISO 13485, GxP, and U.S. regulations, and ensures accurate maintenance and release records.

Oversee and optimize backend semiconductor manufacturing processes, including assembly, packaging, testing, and quality control. Coordinate cross-functional teams, evaluate equipment and tooling, monitor performance and quality metrics, implement corrective actions, maintain process documentation, ensure safety and compliance, and evaluate new technologies to improve efficiency, yield, cycle time, and product quality.

Supports end-to-end quality activities across product, supplier, and QMS processes. Performs inspections, monitors quality metrics, investigates nonconformities and complaints, supports validation and CAPA activities, maintains quality records, assists with audits and management reviews, and participates in supplier qualification and corrective actions. The role ensures compliance with medical device quality standards and regulatory requirements while driving continuous improvement.

Supports business intelligence administration and roadmap execution through report design, development, testing, implementation, and support. Develops actionable reports, maintains ETL packages using Microsoft solutions, deploys notifications, analyzes business needs, and collaborates with IS teams and stakeholders. The role requires SAP BI reporting expertise, knowledge of ERP and data warehouse systems, strong analytical and communication skills, and the ability to manage changing priorities and complex projects.

Leads quality engineering activities across medical device development, manufacturing, inspection, and customer use. Responsibilities include quality system compliance, DHR and DMR review, CAPA and NCR resolution, root-cause investigations, risk analysis, supplier issues, audits, product safety certifications, statistical quality monitoring, and continuous improvement. The role collaborates with engineering, manufacturing, regulatory, suppliers, customers, certification agencies, and external laboratories to ensure product quality and regulatory compliance.

Perform general ledger accounting, month-end close, expense and bank reconciliations, prepare accruals and journal entries, support Procurement/AP system, audits, and finance process improvements for multiple international entities.

Sell Masimo medical devices across São Paulo, converting hospital accounts through demonstrations, negotiations, tenders, and value-based sales. Build relationships with physicians, administrators, biomedical engineers, purchasing managers, distributors, and OEM partners. Provide product training, market and competitive intelligence, sales forecasts, and expense management while supporting account conversion strategies in a highly competitive market.

Develop hospital and private healthcare accounts, drive sales of patient monitoring technologies, manage the full sales cycle, conduct product demonstrations and clinical evaluations, provide customer training, support implementations, and build relationships with clinicians and decision-makers. The role also includes account planning, forecasting, clinical research support, event representation, competitor monitoring, and regular territory travel.

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.

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.

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+.

The IT & IS Systems Engineer analyzes business needs and supports systems while ensuring efficient hardware, software, and network operations.

The Marketing Director oversees product and brand management, drives product launches, conducts market research, develops marketing strategies, and collaborates with various teams to optimize outreach and engagement.

The Quality Engineer manages quality engineering tasks, ensuring product quality standards during manufacturing, and supports process validation and quality assurance activities.

Responsible for managing interconnect projects, collaboration with cross-functional teams, project planning, risk assessment, and quality assurance.