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Manager Medical Device Software Engineer Jobs in Michigan

aspensurgical

Sr Design Engineer

Caledonia, MI

... 62304 (Medical Device Software Lifecycle Requirements) preferred. * Strong familiarity with the ... Project management experience to effectively manage and complete multiple projects simultaneously

Utilidata

Software Engineer, On Device

Ann Arbor, MI · On-site +1

$120K - $150K/yr

Data compression and schema management for device time series data * Experience implementing and ... medical condition, pregnancy or childbirth, sexual orientation, genetics, genetic information ...

Aspen Surgical

Sr Design Engineer

Caledonia, MI · On-site

... 62304 (Medical Device Software Lifecycle Requirements) preferred. * Strong familiarity with the ... Project management experience to effectively manage and complete multiple projects simultaneously

Danaher

Software Engineer Internships

Warren, MI · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Lansing, MI · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Allendale, MI · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Kalamazoo, MI · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Detroit, MI · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Ann Arbor, MI · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Flint, MI · On-site

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering ...

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All JobsManager Medical Device Software Engineer JobsManager Medical Device Software Engineer Jobs in Michigan

Manager Medical Device Software Engineer information

What are the key skills and qualifications needed to thrive as a Manager Medical Device Software Engineer, and why are they important?

To thrive as a Manager Medical Device Software Engineer, you need expertise in software development, medical device regulations (such as FDA or ISO 13485), and a background in engineering or computer science, often supported by advanced degrees or certifications. Familiarity with tools like version control systems (e.g., Git), embedded systems platforms, and quality management software is essential, along with understanding regulatory documentation processes. Strong leadership, effective communication, and problem-solving abilities distinguish top performers in this role. These skills are crucial for ensuring safe, compliant, and innovative medical device software development while leading teams to deliver high-quality products.

Which medical device companies pay the best?

Medical device companies known for high compensation for roles like Medical Device Software Engineer include large multinational firms such as Medtronic, Abbott, and Boston Scientific. Salaries are often influenced by experience, certifications, and location, with senior engineers and managers typically earning higher wages. Competitive benefits and bonuses are also common in top-paying companies in the industry.

What engineer makes $500,000 a year?

A senior medical device software engineer with extensive experience, specialized skills, and leadership responsibilities can earn $500,000 or more annually. Such high salaries are typically found in senior roles at large companies, often involving advanced certifications, complex project management, and significant contributions to product development or regulatory compliance.

What engineers make $300,000 a year?

Senior medical device software engineers, especially those with extensive experience, specialized skills, and certifications, can earn $300,000 or more annually. High compensation is often associated with leadership roles, working in regulated environments, or in companies with significant product complexity and responsibility.

How does a Manager Medical Device Software Engineer typically collaborate with cross-functional teams during product development?

A Manager Medical Device Software Engineer frequently works alongside teams such as regulatory affairs, quality assurance, hardware engineering, clinical specialists, and marketing. They coordinate software development activities to ensure compliance with industry standards and regulatory requirements, while also aligning software features with clinical and business needs. These managers often lead design reviews, facilitate risk assessments, and ensure effective communication between software engineers and non-technical stakeholders. This collaborative environment is essential for delivering safe, effective, and user-friendly medical devices.

What does a Manager Medical Device Software Engineer do?

A Manager Medical Device Software Engineer oversees teams that design, develop, and maintain software for medical devices. They ensure that the software complies with regulatory standards, works reliably, and meets the needs of healthcare professionals and patients. In addition to technical leadership, they coordinate with cross-functional teams, manage project timelines, and mentor engineers. Their role is critical in ensuring products are both safe and effective for use in medical settings.

Can I make 200k a year as a software engineer?

Manager Medical Device Software Engineers with extensive experience, specialized skills in embedded systems, regulatory knowledge, and certifications can potentially earn $200,000 or more annually, especially in high-cost regions or with senior roles. Salary levels depend on factors such as location, company size, and individual expertise, with senior positions often exceeding this threshold.
What are the most commonly searched types of Medical Device Software Engineer jobs in Michigan? The most popular types of Medical Device Software Engineer jobs in Michigan are:
What are popular job titles related to Manager Medical Device Software Engineer jobs in Michigan? For Manager Medical Device Software Engineer jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Manager Medical Device Software Engineer jobs in Michigan look for? The top searched job categories for Manager Medical Device Software Engineer jobs in Michigan are:
What cities in Michigan are hiring for Manager Medical Device Software Engineer jobs? Cities in Michigan with the most Manager Medical Device Software Engineer job openings:
Manager Medical Device Software Engineer jobs near you
Staff Software Systems Engineer- Medical Device

Staff Software Systems Engineer- Medical Device

Stryker

Portage, MI • On-site

$102K - $171K/yr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Work Flexibility: Hybrid

Stryker is seeking a technical leader responsible for guiding the development of complex, software-driven medical device systems. This position supports our Neurosurgical group and operates at the intersection of systems engineering and software development, ensuring alignment among stakeholder needs, system architecture, regulatory requirements, and product implementation. The role also ensures end-to-end traceability from stakeholder needs through software requirements and verification, in full compliance with design controls and the software development lifecycle.
What You Will Do

  • Translate user, clinical, and system-level needs into clear, traceable high level software requirements.

  • Contribute to early concept development and system architecture decisions, driving resolution of complex design challenges.

  • Drive software system integration, verification, and validation activities to ensure performance, quality, and safety objectives are met.

  • Establish and maintain end-to-end traceability across requirements, architecture, implementation, testing, and defect management.

  • Coach and guide teams in developing high-quality, testable, and compliant requirements.

  • Partner with Agile software development teams to prioritize features and enable efficient, predictable delivery.

  • Collaborate cross-functionally with Quality, Regulatory, Project Management, and multi-disciplinary R&D teams to ensure alignment and execution.

  • Support Voice of Customer (VOC) activities and incorporate clinical and customer insights into system design and development.

  • Contribute to Design History File (DHF) documentation and ensure adherence to medical device regulations, design controls, and quality system requirements.

What You Need (Required Qualifications)

  • Bachelor's degree in Software Engineering/ Computer Science or related discipline & 4+ years of work experience


Preferred Qualifications (Strongly Desired)

  • Experience developing and optimizing complex software systems.

  • Advanced knowledge of Requirements Management and System Modeling Tools.

  • Ability to communicate complex technical concepts and plans clearly.

  • Experience influencing SDLC and ALM/traceability processes and best practices.

  • Ability to estimate effort, timelines, and resourcesfor software implementation.

  • Understanding of regulatory and compliance requirementswithin the SDLC.

  • Knowledge of software analysis techniques, including static/dynamic analysis and code coverage.

$102,600 - $171,000 USD Annual

Travel Percentage: 30%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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