Jobs at Merit Medical Systems, Inc.

Assembles medical devices on rotating production lines, performs visual and in-process inspections, rejects nonconforming products, picks and verifies orders, prepares shipments, and boxes products. The role requires following written and verbal instructions, meeting line-rate expectations, maintaining accuracy, working safely, and performing repetitive tasks requiring fine motor skills. Overtime may be required, with lifting up to 50 pounds and exposure to noise, chemical vapors, and soldering fumes.

Performs medical device assembly, visual and in-process quality inspection, order picking, shipment preparation, labeling, and boxing. Follows work instructions, safety standards, and production line requirements while meeting line-rate expectations. The role requires attention to detail, fine motor skills, basic math, accurate product identification, teamwork, and dependable attendance. Overtime may be required, with lifting up to 50 pounds and exposure to noise, chemical vapors, and soldering fumes.

Assists with environmental, health, and safety program development, training, incident investigations, audits, regulatory compliance, hazardous waste coordination, environmental sampling, and corrective action tracking in a high-volume manufacturing environment. Maintains EHS records, investigates root causes, supports injured-worker processes, and recommends measures to mitigate unsafe or hazardous conditions.

The description does not specify day-to-day responsibilities. The role is a Principal Engineer position at Merit Medical, an organization focused on developing innovative medical devices that improve patient outcomes.

Leads global medical device recalls, corrections, removals, withdrawals, and field safety corrective actions. Coordinates cross-functional execution, customer notifications, product recovery, reconciliation, effectiveness checks, regulatory submissions, and recall closure. Maintains inspection-ready documentation, monitors performance metrics, supports adverse event reporting, and ensures compliance with FDA, EU MDR, ISO, Canadian, Australian, and other global medical device requirements.

Lead and maintain the site Quality Management System (ISO 9001/13485), ensure regulatory compliance, manage QA team, support production floor quality, drive corrective/preventive actions, lead audits and product investigations, and enable new product transfers.

Delivers clinical and product training for customers and employees, provides field case support, assesses competencies, develops curricula, answers clinical questions, troubleshoots product issues, and supports sales and marketing education. The role serves as a clinical expert, creates training materials and technical papers, supports market research trials, and coordinates clinical education events and CEU programs. It requires substantial hands-on medical experience, preferably in endoscopy or general surgery.

Sells and demonstrates medical devices to new and existing hospital and clinical accounts across Denmark. Responsibilities include prospecting, account management, pricing and contract preparation, customer satisfaction follow-up, resolving delivery issues, preparing custom kit drawings, reporting sales results, and identifying opportunities to grow revenue and market share. The role requires extensive travel, strong presentation and communication skills, independent work, and fluency in Danish and English.

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.

Provides comprehensive HR support to designated client groups, including employee relations, coaching, investigations, performance management, policy guidance, compliance, workforce analytics, training, and organizational change initiatives. Partners with leaders, supports employee lifecycle activities, conducts exit interviews, improves HR processes, and leads business projects. Requires international HR experience, strong employee relations expertise, Dutch and English fluency, and proficiency with Workday and advanced Excel.

Supports sales, supply chain, finance, and office administration activities. Manages government e-procurement product listings, sales orders, invoices, shipments, inventory adjustments, stock reporting, master data, warehouse stock takes, payment requests, office procurement, vendor coordination, records, meetings, and document approvals. Coordinates with sales, logistics, finance, customer service, vendors, and international teams.

Sells and demonstrates Merit medical devices to new and existing healthcare accounts across the Johannesburg territory. Responsibilities include prospecting, account management, customer satisfaction follow-up, pricing and contract preparation, sales growth, issue resolution, customized kit drawings, product training, competitive knowledge, reporting, and extensive travel. Requires at least five years of direct sales experience, preferably in medical products, strong presentation and communication skills, computer proficiency, independence, organization, and fluency in English.

Develops technical documentation and training curricula for corporate software systems and processes. Delivers classroom and video-based training, evaluates effectiveness through certifications, appraisals, and audits, and ensures compliance with regulations and company policies. Coordinates documentation changes, retraining, and ECNs while collaborating cross-functionally to improve training systems and meet stakeholder needs.

Presents and sells medical device products to new and existing accounts, demonstrates products to clinicians, maintains customer relationships, prepares pricing contracts and customized drawings, resolves delivery or manufacturing issues, coordinates with marketing and sales teams, reports sales results, and travels extensively to meet clients and achieve sales goals.

Manages technical projects from scope definition through delivery, coordinating internal resources, vendors, stakeholders, budgets, schedules, risks, and documentation. Develops project plans, tracks performance, reports changes, maintains stakeholder relationships, and supports process, systems, and equipment training. Requires strong communication, analytical, organizational, problem-solving, and time-management skills, plus proficiency with business software. Oracle ERP experience is preferred.

Independently performs controls and mechatronic engineering assignments involving automation, technical evaluations, prototypes, engineering change notices, and nonconformance material reports. Applies analytical and scientific principles to problem solving, investigates technical variables, supports special projects, and may supervise engineers or technicians. Collaborates with engineering teams while applying applicable United States and international standards.

Manage accounting close, financial reporting, payroll, VAT returns, tax coordination, reconciliations, audits, SOX 404 compliance, and financial analysis for multiple European entities. The role also supports regional finance leadership, maintains accounting records, develops process improvements using lean tools, prepares management reports, and contributes to special projects.

Leads software quality assurance for embedded, application, cloud, and manufacturing software used in medical devices. Develops quality plans, performs software risk analyses, reviews validation documentation and traceability, qualifies suppliers, investigates software issues and field events, and manages changes, regression testing, vulnerabilities, patching, and post-market risk updates. Ensures compliance with medical-device software standards, FDA guidance, design controls, and quality-system requirements.

Manage a sales territory in Germany by presenting and selling Merit medical devices to new and existing accounts, maintaining client relationships, resolving delivery/manufacturing issues, preparing pricing/contracts and custom drawings, coordinating with marketing and sales teams, reporting monthly sales results, and traveling extensively to meet sales targets and improve customer satisfaction.

Designs and develops endovascular medical devices and delivery systems. Leads technical problem solving, creates prototypes and ECNs, supports manufacturing and testing, may supervise technicians, and applies process validation (IQ/OQ/PQ) and materials expertise.