Digital, artifact-driven evidence management * Agile and DevOps-aligned workflows * AI-enabled ... Medical device software standards (SaMD, Digital Health IT) and frameworks (e.g., IEC 62304 ...
Digital, artifact-driven evidence management * Agile and DevOps-aligned workflows * AI-enabled ... Medical device software standards (SaMD, Digital Health IT) and frameworks (e.g., IEC 62304 ...
Lead embedded software development activities across the full medical device lifecycle in ... Familiarity with risk management processes (e.g., ISO 14971) and design control practices.
Lead embedded software development activities across the full medical device lifecycle in ... Familiarity with risk management processes (e.g., ISO 14971) and design control practices.
Director, Software Architecture & Engineering
Center Valley, PA · On-site +1
$239K/yr
IEC 62304 (Medical Device Software Lifecycle) * ISO 14971 (Risk Management) * GDPR / HIPAA (as ... Engineering Execution & Quality * Lead cross-functional engineering teams (software, firmware ...
Director, Software Architecture & Engineering
Center Valley, PA · On-site +1
$239K/yr
IEC 62304 (Medical Device Software Lifecycle) * ISO 14971 (Risk Management) * GDPR / HIPAA (as ... Engineering Execution & Quality * Lead cross-functional engineering teams (software, firmware ...
Medical Device Testing Engineer Billerica, MA - Full Time
Billerica, MA · On-site
$140K - $160K/yr
Risk Management Plans (RMP) * Risk Management Reports (RMR) * Risk Management Files (RMF ... Support software lifecycle quality activities in accordance with IEC 62304. * Participate in ...
Medical Device Testing Engineer Billerica, MA - Full Time
Billerica, MA · On-site
$140K - $160K/yr
Risk Management Plans (RMP) * Risk Management Reports (RMR) * Risk Management Files (RMF ... Support software lifecycle quality activities in accordance with IEC 62304. * Participate in ...
Medical Device Testing Engineer Billerica, MA - Full Time
Billerica, MA · On-site
$140K - $160K/yr
Risk Management Plans (RMP) * Risk Management Reports (RMR) * Risk Management Files (RMF ... Support software lifecycle quality activities in accordance with IEC 62304. * Participate in ...
Quick apply
Medical Device Testing Engineer Billerica, MA - Full Time
Billerica, MA · On-site
$140K - $160K/yr
Risk Management Plans (RMP) * Risk Management Reports (RMR) * Risk Management Files (RMF ... Support software lifecycle quality activities in accordance with IEC 62304. * Participate in ...
R&D Software Engineer - Cybersecurity III
Little Canada, MN · On-site
$40 - $42/hr
... pair generation and management, and X.509 certificate creation, signing, and validation ... medical device development processes Required Qualifications * Bachelor's degree in Computer ...
R&D Software Engineer - Cybersecurity III
Little Canada, MN · On-site
$40 - $42/hr
... pair generation and management, and X.509 certificate creation, signing, and validation ... medical device development processes Required Qualifications * Bachelor's degree in Computer ...
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$115K - $152K/yr
Connectivity and Data Management: * Ensure the software can connect to the internet. * Implement ... Experience working in the medical device industry. * Familiarity with Agile development ...
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$115K - $152K/yr
Connectivity and Data Management: * Ensure the software can connect to the internet. * Implement ... Experience working in the medical device industry. * Familiarity with Agile development ...
Principal Software Engineer - Medical Instrumentation
Merrimack, NH · On-site
$138K - $185K/yr
... regulated medical device software, working closely with various engineering teams to ensure ... Software Development Plans (SDP), Software Configuration Management Plans (SCMP), Software ...
Principal Software Engineer - Medical Instrumentation
Merrimack, NH · On-site
$138K - $185K/yr
... regulated medical device software, working closely with various engineering teams to ensure ... Software Development Plans (SDP), Software Configuration Management Plans (SCMP), Software ...
Senior Engineering Manager, Device Software
San Francisco, CA · On-site
$240K - $360K/yr
The Opportunity Hinge Health is looking for a Senior Engineering Manager to lead a software engineering team inside Hardware R&D, focused on the software systems behind a connected medical device ...
Senior Engineering Manager, Device Software
San Francisco, CA · On-site
$240K - $360K/yr
The Opportunity Hinge Health is looking for a Senior Engineering Manager to lead a software engineering team inside Hardware R&D, focused on the software systems behind a connected medical device ...
... source control management, build processes, testing, and operations experience - Hands-on ... Amazon also offers comprehensive benefits including health insurance (medical, dental, vision ...
... source control management, build processes, testing, and operations experience - Hands-on ... Amazon also offers comprehensive benefits including health insurance (medical, dental, vision ...
Software Engineer III
$57 - $76.50/hr
Analyzing and verifying medical device designs. * *Writing detailed automated and manual test ... Plans and manages assignments of significant scope; directs other engineers. Communicates at all ...
Software Engineer III
$57 - $76.50/hr
Analyzing and verifying medical device designs. * *Writing detailed automated and manual test ... Plans and manages assignments of significant scope; directs other engineers. Communicates at all ...
Senior Software Test Engineer - Embedded Software (Manual & Automation, Medical Devices) (Hybrid-...
Acton, MA · Hybrid
$97K - $145K/yr
Develop and extend protocols and plans as device features evolve. * Participate in product design ... The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery ...
Senior Software Test Engineer - Embedded Software (Manual & Automation, Medical Devices) (Hybrid-...
Acton, MA · Hybrid
$97K - $145K/yr
Develop and extend protocols and plans as device features evolve. * Participate in product design ... The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery ...
... management, build processes, testing, and operations experience - Bachelor's degree in computer ... Amazon also offers comprehensive benefits including health insurance (medical, dental, vision ...
... management, build processes, testing, and operations experience - Bachelor's degree in computer ... Amazon also offers comprehensive benefits including health insurance (medical, dental, vision ...
Sr. Software Quality Engineer
Irvine, CA · On-site
In-depth knowledge of relevant medical device regulations and standards, including FDA 21 CFR Part ... Proficiency with test management tools (e.g., Polarion, Jira, Azure DevOps) and defect tracking ...
Sr. Software Quality Engineer
Irvine, CA · On-site
In-depth knowledge of relevant medical device regulations and standards, including FDA 21 CFR Part ... Proficiency with test management tools (e.g., Polarion, Jira, Azure DevOps) and defect tracking ...
... for connected medical device software systems, ensuring scalability, reliability, and ... management, enabling highly effective project teams. • Proven self-starter who runs towards ...
... for connected medical device software systems, ensuring scalability, reliability, and ... management, enabling highly effective project teams. • Proven self-starter who runs towards ...
Engineering Project Manager (Medical Device) - Hybrid Duration: 12 Months Location: Skaneateles, NY ... project management software). • Engineering Principles: Strong foundation in engineering ...
Quick apply
Engineering Project Manager (Medical Device) - Hybrid Duration: 12 Months Location: Skaneateles, NY ... project management software). • Engineering Principles: Strong foundation in engineering ...
Sr. Manager, Medical Device Cyber Security
Chicago, IL · On-site
$150K - $210K/yr
Partner with R&D and engineering teams to embed secure-by-design principles and Secure Software Development Life Cycle (SSDLC) practices into medical device development. * Define and manage the ...
Sr. Manager, Medical Device Cyber Security
Chicago, IL · On-site
$150K - $210K/yr
Partner with R&D and engineering teams to embed secure-by-design principles and Secure Software Development Life Cycle (SSDLC) practices into medical device development. * Define and manage the ...
Sr. Manager, Medical Device Cyber Security
Chicago, IL · On-site
$150K - $210K/yr
Partner with R&D and engineering teams to embed secure-by-design principles and Secure Software Development Life Cycle (SSDLC) practices into medical device development. * Define and manage the ...
Sr. Manager, Medical Device Cyber Security
Chicago, IL · On-site
$150K - $210K/yr
Partner with R&D and engineering teams to embed secure-by-design principles and Secure Software Development Life Cycle (SSDLC) practices into medical device development. * Define and manage the ...
As an Device Software Development Engineer on the Amazon Leo Government (ALG) team, you will design and develop embedded software for Amazon Leo's satellite and ground systems. You'll work on fault ...
As an Device Software Development Engineer on the Amazon Leo Government (ALG) team, you will design and develop embedded software for Amazon Leo's satellite and ground systems. You'll work on fault ...
Device Software Engineer, Gateway/Embedded Linux
San Francisco, CA · On-site
$123K - $210K/yr
... manage external partners, define architecture, and lead the implementation * The regulatory ... on medical, dental, vision with options for additional coverage. Parental leave up to twenty four ...
Device Software Engineer, Gateway/Embedded Linux
San Francisco, CA · On-site
$123K - $210K/yr
... manage external partners, define architecture, and lead the implementation * The regulatory ... on medical, dental, vision with options for additional coverage. Parental leave up to twenty four ...
Manager Medical Device Software Engineer information
See salary details
$99.5K - $108.7K
1% of jobs
$108.7K - $117.9K
0% of jobs
$117.9K - $127K
2% of jobs
$127K - $136.2K
2% of jobs
$136.2K - $145.4K
2% of jobs
$145.4K - $154.6K
3% of jobs
$154.6K - $163.8K
4% of jobs
$168.6K is the 25th percentile. Wages below this are outliers.
$163.8K - $173K
19% of jobs
The median wage is $175.3K / yr.
$173K - $182.1K
64% of jobs
$182.1K - $191.3K
1% of jobs
$191.3K - $200.5K
1% of jobs
$99.5K
$169.4K
$200.5K
How much do manager medical device software engineer jobs pay per year?
What are the key skills and qualifications needed to thrive as a Manager Medical Device Software Engineer, and why are they important?
How does a Manager Medical Device Software Engineer typically collaborate with cross-functional teams during product development?
What does a Manager Medical Device Software Engineer do?
- Human Factors Engineer Medical Device
- Internship Medical Device Startup
- Medical Device Development Engineer
- Senior Complaint Handling Medical Device
- Process Engineer Medical Device
- Medical Device Regulatory Compliance
- Entry Level Pharma Strategy
- Contract Quality Engineer Medical Device
- Mechanical Design Engineer Medical Device
- Device Test

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 28 days ago
Siemens Healthineers rating
8.5
Based on 87 frontline employees who took The Breakroom Quiz
66th of 430 rated machine equipment manufacturers
Job description
Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.
At Varian, a Siemens Healthineers company, we are committed to creating a "World Without Fear of Cancer". As part of the PTP (Processes, Technology, and Performance) - Processes Team, this role will play a critical part in shaping how software products for medical devices are developed, documented, and continuously improved across a global organization.
This position focuses on process development, governance, and continuous improvement for software design and development lifecycle activities. The role partners with global product development teams to ensure processes are efficient, compliant, and aligned with regulatory standards, while also advancing modernization initiatives such as digitalization and AI-enabled process innovation.
Key Responsibilities
- Process Development & Governance
- Author, update, and maintain procedures and work instructions supporting software design and development processes.
- Ensure processes support controlled, planned, and documented software development across the full product lifecycle (concept through support).
- Align process documentation with key design control elements, software safety and cybersecurity considerations.
- Support organizational readiness for audits and regulatory inspections by ensuring documentation and processes are complete and traceable.
- Software Development Lifecycle (SDLC) Support
- Partner with engineering and product teams to ensure processes support lifecycle phases (Concept and planning, Iterative development, Verification and validation, Release and design transfer).
- Support process alignment with agile practices (Iterative development cycles, Backlog management and user stories, Definition of Done (DoD) and release readiness).
- Collaborate with global stakeholders including R&D, Quality Assurance, Regulatory Affairs, Product Management, and DevOps.
- Facilitate working sessions to understand how teams execute development activities and identify improvement opportunities.
- Support alignment across distributed teams (North America, Europe, India, China).
- Process Improvement & Digitalization
- Identify inefficiencies and drive continuous improvement initiatives in software development processes.
- Contribute to transformation toward:
- Digital, artifact-driven evidence management
- Agile and DevOps-aligned workflows
- AI-enabled process tools and insights
Required Qualifications
- Bachelor's degree in Engineering, Computer Science, Quality, or related field
- 3-10 years of experience in:
- Medical device industry (preferred), or regulated software development
- Software development lifecycle (SDLC), Agile, or DevOps environments
- Understanding of:
- Software requirements, architecture, and testing concepts
- Design controls (e.g., requirements, V&V, traceability)
- Medical device software standards (SaMD, Digital Health IT) and frameworks (e.g., IEC 62304 concepts)
- Experience authoring or contributing to:
- Procedures, work instructions, or technical documentation
- Interest or experience in:
- Digital transformation, process automation, or AI tools
Key Skills & Competencies
- Process orientation: Ability to translate complex development practices into structured, scalable processes
- Technical literacy: Working knowledge of software development and system lifecycle concepts
- Collaboration: Strong ability to work across global, cross-functional teams
- Facilitation: Ability to lead discussions, workshops, and process alignment sessions
- Communication: Strong writing skills with attention to clarity, compliance, and structure
- Analytical thinking: Evaluate workflows and identify opportunities for improvement
- Proactive mindset: Driven to improve processes and enable organizational success
Why Join Us?
This role offers a unique opportunity to:
- Influence how medical device software is developed at scale
- Partner with global engineering, quality, and cross-functional teams
- Contribute to digital transformation initiatives including AI-enabled processes
- Build broad domain knowledge across product development
- Grow into multiple career paths (process leadership, quality, product development, or digital transformation)
Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.
How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
To find out more about Siemens Healthineers businesses, please visit our company page here.
The base pay range for this position is:
$109,920 - $151,140
Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.
If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.
Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.
EEO is the Law: Applicants and employees are protected under Federal law from discrimination. To learn more, click here.
Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.
If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you're unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.
California Privacy Notice: California residents have the right to receive additional notices about their personal information. To learn more, click here.
Export Control: "A successful candidate must be able to work with controlled technology in accordance with US export control law." "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations."
Data Privacy: We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started.
Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site.
To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.
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