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.

Position Title: Senior Test Engineer

A Day in the Life

This engineering position is part of a team of around 10 people and requires experienced technical skills and ability to plan, perform and document characterization and Design Verification testing for single use devices within the Renal Care Solution business.
The position is based in Mirandola (MO), Italy.
Position Responsibilities

• Create and develop DVT Plan, Product Test Protocols and Reports documentation to ensure product design meets specifications and subsystem requirements also in accordance with the reference standards
• Collaborate with developing team to define test purposes and acceptance criteria and perform characterization/feasibility testing
• Execute Performance and Physical Testing using laboratory equipment (dynamometer, leak tester, manometer, etc.). Statistical data analysis of test results
• Develop Work Instructions for Test Methods and perform test method validation activities, including MSA; perform testing for validation and writing the relative documentation
• Equipment Qualification and SW Tool Validation
• Have a focus on objectives to meet the assignments and contribute to the achievement of projects goals
• Work in a team and collaborate with different sites and disciplines (Design Quality, System, Regulatory, Human Factor teams)

Must Have

• BS in Biomedical Engineering, Material Engineering, Chemical Engineering, Chemistry with minimum 4 years of experience in Medical Device product design, verification, validation

Skills Required

• Familiarity with medical device regulatory environment including FDA regulations and MDR
• Knowledge of statistical techniques and tools (use of Minitab, DOE, Statistical Sampling, etc.)
• Ability to work in team and good collaboration attitude
• Methodical, critical thinking and analytical approach to solve issues
• Result-oriented attitude to the planned timelines
• Good oral and written communication and interpersonal skills
• Fluent English, oral and written

Nice to Have

• Previous experience with dialysis single use devices (Peritoneal Dialysis)
• Previous experience with combo-product
• Previous work experience in testing laboratory environment
• Experience with submission of products to FDA
• Knowledge of reference standards (ISO 80369-1/7/20, ISO 8536-4/8/10, ISO 11607-1/2, ISO 15747

Why Work with Us?
Working here is highly rewarding – we have the privilege of helping kidney patients experience greater freedom, improved outcomes and a renewed passion for life.
It’s essential our team members feel valued, supported and empowered too. That’s why we provide a comprehensive total rewards package and opportunities to grow, develop and give back to the communities where we live and work – helping you reach your potential and enjoy a career full of life-changing possibilities.

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.

Is this is the position you were waiting for? Apply here!