Chief Systems Engineer, Benchtop Blood Gas
10 hours ago
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
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.
Responsibilities
This role demands a highly integrated focus on troubleshooting, verification, and technical stewardship, encompassing both current execution and architectural integrity:
- Function as the chief technical escalation point for system hardware and complex electromechanical interfaces, diving into the most intractable integration, testing, and performance challenges for current prototypes.
- Provide critical technical leadership and expertise to support the V&V team, ensuring test protocols are robust, data is technically sound, and complex failures identified during testing are rapidly investigated and resolved.
- Lead and execute advanced fault tree analyses (FTAs) and drive root cause investigations for complex system failures, translating findings into actionable design changes that maintain architectural integrity.
- Review and approve major design change requests that impact critical system interfaces, performance, or regulatory compliance, acting as a technical steward to prevent architectural degradation in the face of in-flight challenges.
- Act as the primary technical conduit between internal R&D and external design/development partners, ensuring alignment on interface specifications, design constraints, and technical decision-making.
- Define and lead the technical strategy for robust, bidirectional knowledge transfer between internal teams and external partners. This includes creating detailed technical training materials, reviewing partner design outputs, and ensuring critical IP and design rationale are successfully internalized.
- Own the meticulous definition, documentation, and rigorous management of all Interface Control Documents.
- Provide expert technical input to system-level FMEAs (Failure Modes and Effects Analysis) and contribute to the ISO 14971 risk management file, focusing on complex, cross-subsystem risks.
- Ensure continuous traceability between the high-level system architecture, subsystem requirements, and verification test cases, particularly as design changes are implemented.
- Serve as a key technical liaison with Assay Scientists, Software Engineering, and Hardware teams, facilitating trade-offs and resolving conflicts at critical system integration points while maintaining system-level coherence.
- Lead the identification and integration of software requirements for IVD platforms, ensuring alignment with system dependencies and compliance with relevant medical device software standards (e.g., IEC 62304, ISO 13485, ISO
- Ensure rigorous definition of platform-level requirements and maintain end-to-end traceability through subsystem specifications and verification testing. Drive alignment between design intent, system architecture, and test coverage.
Required Knowledge/Skills, Education, and Experience
- Minimum a Bachelor's degree in a technical field (e.g., Electrical, Mechanical, Systems or Biomedical Engineering, Computer Science, or equivalent). Advanced degrees preferred.
- Minimum 15+ years of progressive experience in an IVD or Medical Device product development environment, with a demonstrable track record in a lead technical role driving complex system integration and V&V.
- Broad experience in systems design and development involving the integration of fluidics, optics, hardware, software, and consumables, specifically for high-reliability Point-of-Care or Benchtop IVD platforms (blood gas experience highly preferred).
- Proven expertise in structured problem-solving methodologies and a strong ability to conduct hands-on, deep-dive technical investigations on complex prototypes.
- Strong working knowledge of a development process consistent with FDA Design Control requirements, ISO 13485, and ISO 14971 Risk Management practices.
- Demonstrated experience in successfully managing and ensuring technical alignment with external design or manufacturing partners.
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:
Min $172,680 - Max $259,020Factors 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 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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