Jobs at Merit Medical Systems, Inc.

This role supports quality engineering for medical devices, focusing on design transfer activities, process validation, and risk management while ensuring compliance with quality standards.

The QA Design Transfer Engineer is responsible for ensuring design outputs are effectively transferred to manufacturing, coordinating risk analysis, and authoring engineering documentation. They also perform root cause analysis and contribute to continuous improvements in product quality and compliance with regulatory standards.

The Senior Manager of Commercial Marketing is responsible for driving growth strategy and execution for the Renal Therapies portfolio, partnering closely with leadership to achieve revenue growth and market expansion. This role requires collaboration with sales, overseeing product launches, and building relationships with key stakeholders to ensure successful market performance.

The Label Engineer I performs routine technical work in engineering tasks, utilizes judgment for technical decisions, and assists in special projects and prototype creation.

Perform quality engineering for molded medical-device products: manage risk documentation, review/approve ECNs, investigate nonconformances, ensure containment, maintain QMS effectiveness, support mold validation and process improvements.

Support development and execution of value-based pricing across global markets. Analyze price-volume tradeoffs, support RFPs and large deals, maintain pricing tools (CPQ), build dashboards, monitor pricing performance, and partner cross-functionally to drive pricing governance and change management.

The Senior Engineer I at Merit Medical works on the design and operation of medical devices, supervising technicians, tackling technical problems, and completing projects with advanced techniques.

Perform basic equipment and parts assembly/installation, prepare test specimens, record engineering data and plots, operate general test equipment, follow established procedures, and support engineers as directed.

Territory Manager responsible for achieving sales targets and market share in South‑East France through daily customer visits, product demonstrations, CRM management, pricing/contracts, coordinating with internal teams, and participating in events and training. Requires strong clinical product knowledge, travel, and reporting to regional sales management.

The Operations Associate I assembles medical devices, performs quality inspections, verifies orders, and adheres to safety standards as part of a production team.

The Operations Associate performs medical device assembly, inspects products, verifies orders, prepares shipments, and adheres to safety standards. Overtime may be required.

Manage trial master file and regulatory documentation, track study progress, support vendors and sites, assist monitors and project managers, coordinate IRB submissions, contribute to trial start-up, conduct, and close-out activities, and perform study systems training.

Lead global post-market surveillance, vigilance, and regulatory compliance for medical devices. Own PMS strategy, signal detection, global vigilance reporting, recalls, HHEs, and post-market reporting deliverables while partnering cross-functionally to drive corrective actions and regulatory interactions.

Manage and optimize Microsoft Dynamics 365 CRM to support commercial operations: configure entities/forms, ensure data quality, oversee integrations (Oracle, BI tools), enable reporting, manage users, deliver training, and advise leadership on CRM strategy.

Lead regulatory strategy and execution for a medical device platform: collaborate with cross-functional teams, ensure global regulatory compliance and submissions, maintain regulatory data, support audits/inspections and due diligence, and coordinate integration of acquisitions while driving continuous improvement in RA processes.

Lead quality engineering for assigned medical device product lines: investigate failures, manage nonconformances, update risk analyses, define inspection plans, trend metrics, drive supplier quality, approve ECNs, and support validation and quality system improvements.

Lead process engineering efforts on night shift to improve equipment reliability, OEE, yield and quality. Manage automation/upgrades, validation, maintenance prioritization, capital spending, cross-functional continuous improvement, and regulatory compliance in a cGMP medical device manufacturing environment.

The Account Executive presents and sells Merit medical products, maintains client relationships, coordinates with marketing and sales staff, and prepares sales reports.

The Senior Clinical Post Market Specialist oversees Post Market Surveillance activities, ensuring compliance with regulations, managing documentation processes, and providing subject matter expertise. They interact with regulatory bodies and lead improvement initiatives based on post-market findings.

Lead benefits administration and continuous improvement, manage open enrollment and lifecycle events, ensure compliance (ERISA/ACA), analyze utilization and costs, maintain Workday accuracy, provide bilingual (Spanish/English) communications and guidance, partner with leaders and vendors, and deliver data-driven recommendations to support budgeting and employee experience.