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
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Work on SPECT, SPECT/CT, and PET/CT systems.
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Collaborate with Manufacturing and Design Engineering teams to support the successful release of imaging systems into production.
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Conduct system-level testing as required, including Customer Acceptance Testing (CUT), Performance Qualifications (PQs), ramp-up activities, and production stop‑gap testing.
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Train production personnel on system assembly, testing, and troubleshooting activities.
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Provide input for work and test instructions.
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Coordinate with support teams to ensure conformance of incoming components.
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Maintain fixtures and tooling, ensuring they are in proper working condition and calibrated according to schedule.
Requirement
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Experience in medical device manufacturing, refurbishment or service.
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Hands on troubleshooting experience with 480v 3 Phase
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Knowledge of assembly and testing processes, including interpretation of technical drawings, schematics, and wiring diagrams; adherence to procedures; software loading; and use of hand tools, power tools, and test equipment.
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Demonstrated troubleshooting proficiency.
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Capable of working independently with minimal guidance and supervision.
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Excellent oral and written communication skills.
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Effective team player with the ability to collaborate across functions.
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Committed to following safe work practices and maintaining a safe work environment.
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Physically able to lift up to 50 lbs.
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Minimum of an associate degree in a technical discipline or equivalent work experience.
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Travel may be required.
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Experience with an integrated system between MI and CT.
Preferred
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Technical knowledge of Molecular Imaging systems and Computed Tomography products.
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Knowledge of radiation safety practices.
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Mastery good documentation practices.
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Command of handling non-conforming material in an FDA regulated environment.
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Experience with an integrated system between MI and CT.
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Associates or Bachelor’s degree in a technical field.
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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:
$76,980 - $105,853
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 [email protected]. 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.”
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