Acute Care Technology Job Summary This position is responsible for supporting electrode product and process sustaining activities through the application of quality engineering skills for medical devices. Focuses on process, equipment, and design verification and validations; working with teams to develop manufacturing and quality processes and define their related tools; troubleshooting and support of manufacturing floor and field issues, and review and approve validations. Essential Job Functions: Review and approve verification and validation protocols and reports. Participate in Change Control review and approval activities as required. Provide technical guidance and oversight to Quality Engineers. Participate in Risk Management process, including the development and maintenance of risk management files, ensuring compliance with ISO 14971. Develop and implement quality plans. Ensure post market surveillance reviews are conducted and reports documented according to schedule. Participate in CAPA efforts, and apply systematic problem-solving methodologies identifying, prioritizing, communicating, and driving resolution of quality issues. Provide key quality trending information and data for Management Review and monthly KPI review, as applicable. Represent quality interests and concerns on project teams. Investigate causes of quality and yield problems identified in the field and throughout the manufacturing and testing processes. Provide critical quality engineering direction to projects with respect to generally accepted quality engineering tools/principles, such as process validation, equipment, test methods, root cause analysis, risk mitigation, process improvement tools, sampling plans, etc. Provide support during regulatory audits and responses to government agency questions. Required/Preferred Education and Experience: Bachelor's Degree in Engineering or technical discipline required 5 Years medical device experience required Knowledge, Skills and Abilities: Proficient with Microsoft Office Suite Familiarity with mechanical and electrical test equipment Knowledge of commonly used concepts, practices, and procedures related to medical device manufacturing Working knowledge of EN ISO 13485, ISO 14971 and FDA QSR for Medical Devices Ability to work in a fast-paced environment High energy problem solver capable of driving items to closure Excellent communication and interpersonal skills (verbal, written and presentation). Understands how to present information dependent on the level of the audience. Ability to effectively manage time, balance multiple task assignments and translate quality requirements into product specifications Understands basic applied statistics, statistical sampling plans and statistical process control Familiar with Minitab Statistical Analysis Software (or equivalent) Preferred Languages: English - Expert Travel Requirements: 5% Travel is required, primarily during working hours Physical Demands: Standing - Occasionally Walking - Occasionally Sitting - Constantly Talking - Occasionally Hearing - Occasionally Repetitive Motions - Frequently ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.