Sr Mechatronics Verification and Validation Engineer

Full-timeSeniorQualityOphthalmology
$115K - $158K/yr(employer-provided)

Description

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.

The Senior Mechatronics V&V Engineer will be part of the R&D organization and an important contributor to the realization of the next generation robotic platform that will change the future of healthcare. You will be a visible technical resource working on development & testing of a complex electro-mechanical system. There will be direct contribution from prototype to verification builds and testing within a regulated medical device development environment. This role is suited for a senior-level R&D engineer with experience working cross functionally to plan V&V activities, perform fixture qualification and test method validation, perform V&V tests, perform statistical analysis, author and review documentations, and support R&D development activities.

Key Responsibilities 

  • Leads the system, subsystem verification activities through completion for a complex electromechanical system 

  • Develops test plans, verification, and validation protocols, and identify levels of resources, in terms of personnel, budget, schedule, and facilities, to accommodate various test efforts including analysis, inspection, demonstration, and test 

  • Develops or refines existing electromechanical fixtures and testers as needed using the mechanical tools (such as SolidWorks) and software (e.g., MATLAB, Simulink, LabVIEW) 

  • Develops test methods, protocols, execute tests, prepare reports and release them via ECOs  

  • Maintains disciplined test, configuration control, documentation, and management processes throughout 

  • Proposes refinements to requirements, and/or test methods, to expedite V&V activities  

  • Supports establishment of traceability matrices for all levels of requirements 

  • Performs hands-on and simulated testing for design verification and test method developments 

  • Analyzes test results. Apply statistical analysis as needed  

  • Identifies and reports out-of-specification results, data, and atypical/unexpected events that occur during tests  

  • Manages issues, provides technical troubleshooting for hardware testing and support defect resolution through root cause analysis (RCA) and corrective measures to prevent recurrence 

  • Performs fixture qualification and test method validation 

  • Communicates information clearly, effectively, and frequently (oral and written) with stakeholders, project team 

  • Manages and delivers assigned projects in collaboration with cross-functional teams within agreed delivery timelines 

 

Qualifications:  

  • Minimum of 7 years’ electromechanical R&D engineering experience, preferably in the medical device industry required. Some years of experience in other heavily regulated industries will be considered. 

  • Bachelor’s and/or Masters degree in Mechanical, Mechatronics, Robotics Engineering or a close field is required 

  • Proven proficiency in developing test methods, protocols, performing tests and releasing relevant documentation is required. 

  • Experienced in fixture and process validation. 

  • Experienced in using statistical tools and software such as Minitab, MATLAB 

  • Must have experience in cross-functional collaboration and technical leadership 

  • Must have hands-on experience in assembly, integration, and test of complex electro-mechanical systems 

  • Must have MATLAB/Simulink proficiency. LabVIEW proficiency is desired. 

  • Demonstratable CAD proficiency a plus. Solidworks preferred 

  • Demonstrable proficiency in statistical data analysis methods / tools, e.g.: Gage R&R, Hypothesis Testing, Tolerance Interval Analysis, Acceptance Sampling, etc. 

  • Must have working knowledge of applicable medical device regulatory standards i.e.: FDA 21CFR 820, ISO 13485, IEC 60601, ISO 14971, etc. 

  • Must have experience in project management including task timeline estimation and work breakdown structures 

  • Outstanding documentation and communication skills required  

  • Proficiency in using MS Office required 

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:

$114,920 - $158,015

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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OphthalmologyQualityNTN GR
Siemens Healthineers

Siemens Healthineers

DIAGNOSTICS

Medical imaging, laboratory diagnostics, and healthcare information technology

LocationGermany - Forchheim
Employees5000+
Open Jobs568

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