Engineering Supervisor

Dettagli della offerta

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.

A Day in the Life


Maintain the product backlog, including user stories, epics, and acceptance criteria, and ensure it is up-to-date and reflects the latest priorities.Make decisions on behalf of stakeholders regarding the priority of features and changes, balancing technical feasibility and business value.Conduct regular meetings with software engineers to track progress, address challenges, and provide guidance.Collaborate with cross-functional teams including Hardware, System and Design Quality engineers to ensure seamless integration of software components into medical devices.Ensure that all software development activities are properly documented in accordance with regulatory requirements and company procedures.Support upper management to review progress and allocate budgets for software development projects.Provide mentorship and guidance to software engineers, fostering their professional development and growth.Promote a culture of collaboration, innovation, and continuous improvement within the software engineering team.Review project timelines and milestones, making adjustments as necessary to meet deadlines and quality standards.Help troubleshoot significantly impact technical issues and provide guidance on resolving software-related problems.Collaborate with cross-functional teams to address any issues that may arise during product development or post-market support.Must Have: Minimum Requirements To be considered for this role, candidates must demonstrate the following qualifications:

Master's Degree in Software Engineering, Computer Science, or a related technical discipline.Minimum of 5 years of professional experience in software development.Fluent English communication skills.Excellent knowledge of C and C++ programming languages.Strong understanding of Design Patterns and Software Architecture Design.Proficiency in event-driven programming.Advanced Knowledge of Arm ArchitecturesGood knowledge of Unit Testing and integration testing paradigms.Proficiency with version control systems, specifically Git.Proficiency in CI/CD pipeline techniques.Nice to Have In addition to the minimum requirements, the following skills and experiences are considered advantageous:

Full life-cycle product development experience in the medical device industry.Proficiency in Agile Program Management with JiraProficiency with QP/C++ framework.Proficiency with Eclipse-based Integrated Development Environment (IDE).Familiarity with the Python programming language.Knowledge of Machine Learning Algorithms.Experience with Static Analysis toolsProficiency with Qt/pyQt Framework.Familiarity with Data Analysis tools including Numpy, Pandas, and Matplotlib.Good understanding of IEC 62304 standards.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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Salario Nominale: Da concordare

Risorsa: Jobleads

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