Test Engineerii
About Mozarc Medical At Mozarc Medical, our vision is to reimagine the future of holistic kidney health technology.
Established in 2023 out of equal investments from DaVita, a leading provider of kidney care services, and Medtronic, one of the world's largest medical device companies, Mozarc Medical offers an exciting and unique start-up experience backed by the support of two long-time industry and market leaders.
Driven by our mission and values, we put our patients at the center of all we do.
Our employees play a key role in developing technology solutions that enrich patients' lives and create meaningful progress in the treatment of kidney disease.
Find your purpose and passion at Mozarc Medical.
A Day in the Life This engineering position is part of a team of about 30 people and requires experienced technical skills and the ability to understand technical documentation in order to design and perform VV tests for products within the Mozarc Medical business.
The position is based in Mirandola, Italy.
Position Responsibilities:Create, implement and develop the product test plans/protocols and generate test reports to ensure product design meets the specifications and quality system requirements also in accordance with the reference standards. Work closely with the system team and developing team to design test descriptions and acceptability criteria. Perform product tests using, if necessary, laboratory tools (multimeter, oscilloscope, etc.
). Perform statistical analysis of test results. Design test methods and perform test method validation activity, including MSA, writing the relative documentation. Provide the test area with parameters for sample testing and specify tests to be performed. Able to work in a global collaborating environment with intensive challenges. Minimum Qualifications:Required: BS in Biomedical Engineering, Computer Engineering, Electronic Engineering, or Mechanical Engineering with a minimum of 2 years of experience in product design VV. Skills required:Knowledge of statistical tools to improve product and process understanding (Minitab, etc.
). Familiarity with the medical device regulatory environment including FDA regulations, MDR, and IEC standards. Able to develop technical solutions to problems that require critical thinking. Must be team-oriented and able to contribute to the successful completion of major programs. Must be able to work with teams remotely and in different geographical locations. Nice to have:Previous work experience on dialysis devices. Previous work experience in a testing laboratory environment. Knowledge of dialysis equipment reference standards (IEC 60601-2-16 and collateral standards). Knowledge of tools for test system development, test automation, and data analysis (LabVIEW, Matlab, Simulink, etc.
). Demonstrated strength in building strong relationships at all levels of the organization, cross-functionally, and with key people external to the organization. Location: Mirandola (MO) – ITALY 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.
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