Senior V&V Test Engineer 

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 good technical skills and ability to understand technical documentation in order to design and perform V&V tests for products within the Renal Care Solutions 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. 

Must Have:

• min Bachelor degree in Biomedical Engineering / Computer Engineering / Electronic Engineering or Mechanical Engineering with minimum of 4 years of experience in product design Validation & Verification 
• Demonstrated strength in building strong relationships at all levels of the organization, cross functionally, and with key people external to the organization. 
• 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. 
• Team-oriented and able to guide the successful completion of major programs. 
• Open to work with teams remotely and different geographical locations. 
• Strong overall communication skills and technical writing skills. 

 
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).