Do you want to join us in helping to fight the world’s most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

At Siemens Healthineers, we offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally.

Our Global Team:

We are a team of more than 72,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what’s possible in healthcare to help improve people’s lives around the world. As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways.

Our Culture:

We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what’s possible, to improve people’s lives around the world.  We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success.

Analyzes and designs work systems in order to support general adherence to agreed standards, in order to ensure humanely and economical production and drives continuous improvement topics.

The successful candidate will participate in a wide variety of semi-complex technical assignments necessary to support the manufacturing of immunochemistry diagnostic tests for the diabetes market.  The incumbent will be responsible to help write and execute validation plans, participate in root-cause analysis efforts, aid in identifying process/equipment improvements, conduct customer complaint investigations as well as other testing as directed.  This person must be highly competent in bench-scale solution preparation and willing to learn specialized testing techniques.  Must also be able to prepare, analyze, and present coherent data for review and summarize results in a technical report.  The medical device industry is highly regulated, and the candidate must be able to function and support the requirements of the regulations.

Major tasks and responsibilities:

Conduct validation and verification activities to ensure project completion within expected parameters and time frame.Design and conduct experiments to identify process issues related to undesirable reagent or manufacturing performance and identify resolutions for those issues. Plan, conduct, analyze, and document experiments necessary to improve manufacturing process capability and reduce costs associated with cassette-based reagent production.Work with Product Support technical leaders to collect and analyze reagent and instrument performance data necessary for product/process improvements; customer complaint and problem investigations; and Marketing/Global Service and Support use.Participate in root-cause analysis and customer complaint investigations.Able to design complex experiments, execute test protocols, and analyze/interpret their results.Apply principals of lean manufacturing and support continuous improvement activities to meet quality, cost and supply requirements.Must be able to verbally communicate clearly and directly with colleagues and provide well-written, coherent progress updates, validation documents, study protocols, and technical reports.Participate in supplier and internal audits; able to interact effectively with key suppliers.

Qualifications:

Preferred Bachelors or Masters in Biochemistry; will consider degree in other science or engineering, with a concentration in Chemistry.2 – 5 years’ experience, preferably in a medical device or related industryStrength in one or more of the following areas: Clinical Chemistry, Immunoassays, Analytical Chemistry, Biostatistics, Manufacturing Process Capability, and Computer Science.Proven experience in successful root cause analysis and resolution of manufacturing or design issues.Demonstrated competence in experimental design and data interpretationWorking knowledge of basic statistics necessary to develop sampling plans and analyze data.Able to prepare and fully understand data analysis reports and testing protocols; able to utilize data collection applications in a laboratory setting.Must be well versed in Office Applications, particularly Excel and Access; experience in Matlab, SAS, or Minitab desired.Some travel (<10%) may be required.

Other characteristics of the successful candidate:

Very organized, detail-orientedHighly self-motivatedAble to work independentlyExcellent analytical, communication, writing, and problem-solving skillsEffective and influential in his/her interactions in team-based assignmentsAble to work well with personnel from different departments, and experience levelsLean Manufacturing experienceDemonstrates good laboratory practices

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.

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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.   

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A Successful candidate must be able to work with controlled technology in accordance with US export control law when required. 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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Equal Employment Opportunity Posters

At Siemens Healthineers, we value those who dedicate their energy and passion to a greater cause. Our people make us unique as an employer in the med-tech industry. What unites and motivates our global team is the inspiration of our common purpose:  To innovate for healthcare, building on our remarkable legacy of pioneering ideas that translate into even better healthcare products and services. We recognize that taking ownership of our work allows both us and the company to grow. We offer you a flexible and dynamic environment and the space to move beyond your comfort zone to grow both personally and professionally. 

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As an equal-opportunity employer we are happy to consider applications from individuals with disabilities.