Engineer II, Design Quality (hybrid)

Position Summary Provide quality support for ICU Medical Consumable development. The Design Quality Engineer II will support activities such as CAPA investigations, design projects, and will ensure compliance with ICU Medical quality system requirements and applicable regulations and standards, such as ISO 13485, ISO 14971, 21 CFR Part 820, and other applicable regulations and standards. Essential Duties & Responsibilities Effectively utilize quality tools and processes such as product and process controls, risk analysis/management tools, validation, design verification, investigations, CAPA data, etc. to assure product quality. Assures conformance with regulations of the FDA and other international regulatory agencies. Supports the development, application, and maintenance of quality standards. Ensure all Quality attributes for design changes are met. Participate in design reviews, test readiness reviews, cross functional teams, risk assessments, design transfers, etc. Ensure that potential product and process risks are evaluated, prioritized, and mitigated to continuously improve product quality. Support any potential internal and/or external audits and inspections. Maintain Design History Files (DHF) up to date as needed. Effectively interact with cross-functional team members. Provide quality support and for on-market product issues. Bring issues to closure and escalating to management for support as necessary. Work special projects as assigned Knowledge & Skills Knowledge of Quality Management Systems and experience linking risk management to all elements of the Quality System (Design Controls, CAPA, Complaints, Document Control, etc.) Knowledge of medical device standards, ISO 13485, MDSAP, EU MDR and ISO 14971. Knowledge in Statistics (Tolerance limits, Cpk, etc.) and Minitab is preferred. Minimum Qualifications, Education & Experience Must be at least 18 years of age Bachelor’s degree in engineering (Electrical, Mechanical, Biomedical) or related field from an accredited college or university is required. Minimum of two years of experience in R&D and/or Quality is required. ASQ CQE certification preferred Work Environment This is largely a sedentary role. This job operates in a professional office environment and routinely uses standard office equipment. Typically requires travel less than 5-10% of the time