Job Description:

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.

 

Position Title: Sr. Principal R&D Controls Engineer

The Sr. Principal R&D Controls Engineer, operating in R&D, will be accountable for system and sub-system design and integration between hardware (electrical, electronics, sensors and mechanical) and software (firmware, embedded and operating applications) and will closely collaborate with all the design, quality and OPS functions inside the organization to ultimately create highly functional complex medical devices.  This individual independently drives, evaluates, selects and applies modern engineering techniques, procedures and tools to design, test and deliver device operating requirements.

A Day in the Life

 

• Provide effective technical leadership to multi-disciplinary product development efforts


• Evaluation and definition of the interfaces between components and media


• Creation of requirements specification for the entire device control loop: HW components & Interfaces, Software, and Mechanical Interfaces


• Development of algorithms for control systems used in complex dialysis machines


• Control Functions improvement (or new development) based on any research project (model Base Design, C Code, Rapid prototyping, …)


• Fluent in using simulations as a tool when needed


• Accountable for performing and reviewing root cause and failure analysis activities and presenting it to involved disciplines to negotiate remediation strategies


• Consider and consolidate internal functional and safety requirements


• Ensure the implementation, verification, and validation of all functional requirements in the project


• As needed, plan and execute function and application testing on HIL (hardware in the loop)


• Support for the handling of test equipment and maintenance and needed test tools


• Works collaboratively with other departments in resolution of development issues from above (System, HW, SW, Architecture etc.)


• Interface to customer (OEM) for all function related issues


• Ideate, evaluate and directs cross-discipline team towards preferred design options to meet product/performance requirements. Collaborates with IP Counsel as needed


• Manages internal and external design partners, suppliers and manufacturers as needed


• Provides regular updates to engineering and product leadership on status and advancements

 

Must Have

 

• Master’s degree in Engineering required


• At least 5 years of working experience in model based designed or HW\SW in the loop testing


• At least 10 years of relevant medical device engineering experience

 

Nice to Have:

 

• Experience in Software Testing using Hardware-In-the-loop and (HIL)/or software-in-the-loop (SIL) Environment


• Development of control algorithms


• Experience in Analyzing test results and identifying actionable intelligence out of the data


• Working knowledge of, and experience in applying, FDA Design Controls and international standards (e.g., Design Controls, 820-CFR, ISO14971, ISO13485, IEC60601, etc.)


• Experience in SW debugging and usage of emulators and debuggers


• Knowledge in C/C++ Programming


• Experience in Testing tools (CANalyzer)


• Knowledge in test automation using Python / Perl / Java / CAPL Scripting in advantage


• PhD in Engineering or Physical Science


• Plan and execute function and application testing on system and HIL/SIL


• Knowledge in configuration management tools/ Git, Clear case


• Extensive Medical Device background


• Speed Goat


• Knowledge of different processor families and their operating environments


• Understanding on Software process methodologies

 

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.

Physical Job Requirements 

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)

 

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 the position you were waiting for?  Apply here!

Salary: $182,500.00

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