... development of complex, software-driven medical device systems. This position supports the ... management. • Coach and guide teams in developing high-quality, testable, and compliant ...
... development of complex, software-driven medical device systems. This position supports the ... management. • Coach and guide teams in developing high-quality, testable, and compliant ...
Staff Software Systems Engineer- Medical Device
$102.60K - $171K/yr
... development of complex, software-driven medical device systems. This position supports our ... Collaborate cross-functionally with Quality, Regulatory, Project Management, and multi-disciplinary ...
Staff Software Systems Engineer- Medical Device
$102.60K - $171K/yr
... development of complex, software-driven medical device systems. This position supports our ... Collaborate cross-functionally with Quality, Regulatory, Project Management, and multi-disciplinary ...
MDR Quality Engineer II - Medical Device
Dexter, MI · On-site
$68.60K - $88.60K/yr
MDR Quality Engineer II - Medical Device Location: Dexter, MI (Fully Onsite) Type: W2 Contract ... documentation management • Cross-functional collaboration with Manufacturing & Product ...
MDR Quality Engineer II - Medical Device
Dexter, MI · On-site
$68.60K - $88.60K/yr
MDR Quality Engineer II - Medical Device Location: Dexter, MI (Fully Onsite) Type: W2 Contract ... documentation management • Cross-functional collaboration with Manufacturing & Product ...
Software Engineer, On Device
Ann Arbor, MI · On-site
$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 ...
Software Engineer, On Device
Ann Arbor, MI · On-site
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Data compression and schema management for device time series data * Experience implementing and ... medical condition, pregnancy or childbirth, sexual orientation, genetics, genetic information ...
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Ann Arbor, MI · On-site
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Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience * We are ... Advisory, PLM Software/Services, Program Management, Solution Architecture Training/Staffing, Cloud ...
Quick apply
Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience
Ann Arbor, MI · On-site
$101.70K - $137K/yr
Integration Engineer (Embedded or Test Engineer)-Automotive/Medical device exprience * We are ... Advisory, PLM Software/Services, Program Management, Solution Architecture Training/Staffing, Cloud ...
Engineering Sales Leader - Medical Device
Detroit, MI · On-site
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Lead, develop, and manage a team of sales professionals to achieve revenue growth and performance ... medical device engineering Compensation & Work Model * Base salary range: $120,075 - $195,000 ...
Quick apply
Engineering Sales Leader - Medical Device
Detroit, MI · On-site
$120.08K - $195K/yr
Lead, develop, and manage a team of sales professionals to achieve revenue growth and performance ... medical device engineering Compensation & Work Model * Base salary range: $120,075 - $195,000 ...
Software Engineer I - Device Drivers
Ann Arbor, MI · On-site
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Manage package builds and deployments * Contribute to documentation and technical design ... 100% paid medical, dental, and vision premiums for full-time employees * 401K plan with a 6% ...
Software Engineer I - Device Drivers
Ann Arbor, MI · On-site
$100.60K - $150.90K/yr
Manage package builds and deployments * Contribute to documentation and technical design ... 100% paid medical, dental, and vision premiums for full-time employees * 401K plan with a 6% ...
Software Engineer I - Device Drivers
$100.60K - $150.90K/yr
Manage package builds and deployments * Contribute to documentation and technical design ... 100% paid medical, dental, and vision premiums for full-time employees * 401K plan with a 6% ...
Software Engineer I - Device Drivers
$100.60K - $150.90K/yr
Manage package builds and deployments * Contribute to documentation and technical design ... 100% paid medical, dental, and vision premiums for full-time employees * 401K plan with a 6% ...
Field Service Technician / Engineer (Medical Device) - 61
Detroit, MI · On-site
$75K - $85K/yr
Proven ability to troubleshoot electro-mechanical systems (NOT just software) * Comfortable working ... Engineer with true medical device repair experience - this is your chance to step into a high ...
New
Quick apply
Field Service Technician / Engineer (Medical Device) - 61
Detroit, MI · On-site
$75K - $85K/yr
Proven ability to troubleshoot electro-mechanical systems (NOT just software) * Comfortable working ... Engineer with true medical device repair experience - this is your chance to step into a high ...
New
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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.
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.
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:
- Polymer Engineering
- Remote Process Engineer From Home
- Urgently Hiring Medical Device Software Engineer
- Electrical Engineer Medical Device
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Full-time
Posted 3 days ago
Job description
Job Summary:
Stryker is seeking a technical leader responsible for guiding the development of complex, software-driven medical device systems. This position supports the Neurosurgical group and ensures alignment among stakeholder needs, system architecture, regulatory requirements, and product implementation.
Responsibilities:
• 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.
Qualifications:
Required:
• Bachelor's degree in Software Engineering/ Computer Science or related discipline & 4+ years of work experience
Preferred:
• 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 resources for software implementation.
• Understanding of regulatory and compliance requirements within the SDLC.
• Knowledge of software analysis techniques, including static/dynamic analysis and code coverage.
Company:
Stryker is a medical technology company that offers products and services in orthopaedics. Founded in 1941, the company is headquartered in Kalamazoo, USA, with a team of 10001+ employees. The company is currently Late Stage.
Stryker is seeking a technical leader responsible for guiding the development of complex, software-driven medical device systems. This position supports the Neurosurgical group and ensures alignment among stakeholder needs, system architecture, regulatory requirements, and product implementation.
Responsibilities:
• 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.
Qualifications:
Required:
• Bachelor's degree in Software Engineering/ Computer Science or related discipline & 4+ years of work experience
Preferred:
• 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 resources for software implementation.
• Understanding of regulatory and compliance requirements within the SDLC.
• Knowledge of software analysis techniques, including static/dynamic analysis and code coverage.
Company:
Stryker is a medical technology company that offers products and services in orthopaedics. Founded in 1941, the company is headquartered in Kalamazoo, USA, with a team of 10001+ employees. The company is currently Late Stage.