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 Da Vita, 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 ability to understand technical documentation in order to design and perform V&V 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 to the references standards.
• Work closely with 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 test area with parameters for sample testing and specifies tests to be performed
• Able to work in global collaborating environment with intensive challenges.

Minimum Qualifications:

• Required: BS in Biomedical Engineering, in Computer Engineering, in Electronic Engineering or in Mechanical Engineering with minimum of 2 years of experience in product design V&V.

Skills required:

• Knowledge of statistical tools to improve product and process understanding (Minitab, etc.).
• Familiarity with 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 different geographical locations.

Nice to have:

• Previous work experience on dialysis devices.
• Previous work experience in 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 (Lab VIEW, 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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