Mechanical Design Engineer II

Minneapolis, Minnesota

Mozarc Medical
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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 position of Mechanical Design Engineer II will research, plan, design, build, verify, validate, and develop mechanical and/or electromechanical products and systems for treatment of kidney disease.

An ideal candidate will be familiar with metals, instruments, controls, actuation, plastics, robots, engines, machine, mechanical, resonance, hydraulic, and/or heat transfer systems for production, transmission, measurement, and use of energy.

Must Have:

  • Requires a Baccalaureate degree in Engineering discipline (Biomedical, Mechanical, Industrial (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. 214.2(h)( 4)(iii)(A) and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.
  • Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience.
  • min 2 years of experience in prototyping and/or 3D printing.
  • Basic understanding of computer aided design (CAD) and design specifications/prints.
  • Basic understanding and experience working with programming languages (e.g., MATLAB, Python, etc.)

Nice to Have:

  • min 2 years of experience in the medical device industry.
  • Familiarity with associated medical device and regulatory standards.
  • Experience working with product lifecycle management databases.
  • Experience working with issue tracking software (e.g., Jira, Zendesk, Backlog, etc.).
  • Experience working with Creo Parametric and/or ANSYS simulation software.
  • Intermediate experience with statistical software (e.g. Minitab, JMP, etc.)
  • Willingness to learn and grow in dynamic teams and cross-collaboration with global team members
  • Ability to work independently and autonomously with moderate guidance from experienced team members and management
  • Highly motivated with enthusiasm to learn new skills based on project and business demands
  • Ability to communicate articulately and efficiently throughout the problem-solving process with fellow team members
  • Ability to communicate effectively with internal and external vendors and suppliers.
  • Superior technical writing, documentation, and note-taking skills.
  • Proficient in using Microsoft Suite of software (Word, Excel, PowerPoint, Visio, OneNote, Teams, etc.)
  • Ability to travel, 10-15% of the time

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.

Date Posted: 24 April 2024
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