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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 Senior QA Design Transfer Engineer participates in design and development activities, ensuring design requirements are met for manufacturing and risk management. They lead analysis meetings, generate engineering change notifications, and mentor teams 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 HRIS Systems Analyst manages UKG Pro and supports Workday HCM, focusing on configuration, training, reporting, and compliance with HR processes.

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.

Provide clinical training on Merit products to various groups, answer clinical questions, support Sales Representatives, and develop training programs for medical device usage.

The Director of Financial Planning and Analysis drives organizational change, provides financial direction, leads budgeting cycles, and implements KPIs to enhance profitability and efficiency.

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.

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