Jobs at Merit Medical Systems, Inc.

Lead development and execution of reimbursement and market access strategies for medical devices. Provide payer, coding, coverage, and health policy guidance; partner with HEOR for evidence planning; analyze reimbursement landscapes; educate internal and external stakeholders; identify and resolve access barriers to support product adoption.

Lead U.S. reimbursement and market access strategy for medical device products. Advise cross-functional teams on coding, coverage, payment pathways, and payer evidence needs. Build payer and stakeholder relationships, identify barriers, design access programs, and deliver reimbursement education to internal and external audiences.

Designs, prototypes, and supports sensors and related systems for medical devices. Independently applies standard engineering techniques, investigates technical variables, writes ECNs, creates prototypes, and may supervise technicians. Works on defined projects under broad direction and ensures compliance with applicable standards.

Maintain and troubleshoot corporate networks: configure switches/routers/firewalls/access points, support LAN/WAN and VoIP, handle tickets, coordinate vendors, participate in projects, and be on-call.

Manage and coordinate production schedules to ensure timely completion of manufacturing work orders. Adjust MPS/MRP, evaluate weekly demands, resolve back-orders, prepare production reports, analyze RCCP vs build plans, attend operations meetings, collaborate with supply planners, and mentor Supply Planner II.

Provide clinical training and support for Merit medical devices to sales teams, cath lab and radiology staff, and physicians. Troubleshoot product issues in the field, document complaints, develop training curricula and materials, assist product rollouts, and liaise between customers and internal teams to improve products and resolve clinical concerns.

Sell and demonstrate Merit oncology products to new and existing clinical accounts, maintain client relationships, prepare pricing/contracts/custom drawings, coordinate with internal teams to ensure timely delivery, report sales activity, and travel extensively to meet sales goals and provide customer feedback for product improvements.

Manage and support global application systems projects, primarily focused on ERP systems like Oracle EBS, ensuring integration and optimized processes. Provide training, create documentation, and collaborate with stakeholders.

Sell Merit Medical devices across assigned territory by building relationships, demonstrating products, preparing custom kits/drawings and pricing, resolving delivery/manufacturing issues, coordinating with sales/marketing, meeting sales targets, reporting monthly, and traveling extensively.

Supervises complaint evaluations and investigations, ensuring compliance with regulatory standards and quality practices. Oversees team performance, provides training, and manages complaint processes.

Assemble and inspect medical devices on rotating production lines, operate sealing and testing equipment, pick and box orders, prepare shipments, and maintain quality and safety standards. Must meet line rates and achieve required certifications within 90 days.

Lead product localization and commercialization for China: identify OEM/ODM partners, manage due diligence and supplier audits, run cross-functional product introduction projects (testing, regulatory support, registration), negotiate commercial agreements, design business models and profitability analyses, and drive sales and lifecycle management for localized medical device products.

The Senior Compliance Manager oversees compliance programs across the EMEA region, ensuring adherence to regulations and improving compliance practices. Responsibilities include risk assessment, policy development, compliance training, investigations, and regulatory knowledge management.

The Senior Director of Quality Assurance leads departments ensuring quality policies, manages quality systems, and collaborates with global teams to enhance operational efficiency and compliance in medical device production.

The Senior Regulatory Specialist develops regulatory strategies for medical device submissions, collaborates with teams, ensures compliance with regulations, and maintains stakeholder relationships.

The Territory Manager will sell medical devices, achieve sales targets, maintain customer relationships, present products, and collaborate with teams. Extensive travel is required.

The Supplier Quality Engineer evaluates and ensures supplier quality and compliance, maintains performance metrics, conducts audits, and resolves issues while coordinating with suppliers and internal teams.

Manage accounts receivable processes including billing, reconciliations, collections, credit limit changes, order releases, invoice dispute resolution, and customer account maintenance to support cash flow and compliance.

The Associate Account Executive assists in the sales process, builds client relationships, presents products, and contributes to sales strategies in the medical devices sector.

Assist in the sales process, build client relationships, present products, prepare reports, and achieve sales goals. Travel is required.