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. This position requires the incumbent to be 100% on-site at the Glasgow location in Newark, Delaware. Join our team now at Siemens Healthineers as a Test Design Professional in the Customer Workflow Testing team within Systems Engineering located in Glasgow, DE. The Test Design Professional position will support the research and development of various LD projects. The individual will bring laboratory knowledge to help advance the quality, reliability, and robustness of Siemens’ next-gen lab diagnostic systems. This position includes development of test methods and protocols, design and support of test systems, issue investigation, and executing various testing methodologies: including Design Validation, Reliability testing, Assay testing and various customer workflow testing. This is classified as 100% onsite as it requires physical presence in the laboratory to perform essential job duties. Responsibilities This is a role well suited for a professional who is self-motivated and eager to grow in their career. As a Test Design Professional, you will be responsible for: * Creating, reviewing, and executing test plans of complex software-enabled, electro-mechanical laboratory equipment. * Preparing software and systems validation and ad-hoc testing protocols, including advising on appropriate samples and acceptance criteria. * Performing sample testing on clinical laboratory systems, following Universal Precaution guidelines (safe management of biohazards). * Supporting execution of test protocols with diligent record keeping and documentation. Will capture anomalies in defect management systems. * Evaluating results of testing, provide analysis and summary including presenting outcomes to technical audiences. * Troubleshooting and analyzing product issues or failures (to include Quality Control failures). Leading or supporting investigations, as appropriate. Determining acceptability of test results. * Providing input for Quality Management systems for Customer Workflow Testing department, following CLIA and ISO standards for Clinical Laboratories, including assisting in creation of new Quality Procedures and/or SOPs. * Responsible for adhering to all laboratory requirements for New and Altered inspections. * Responsible for all safety measures, as issued and outlined by Site EHS. * Responsible for maintaining, and calibration, of test equipment. * Ability to work in a laboratory setting for extended periods of time. * Responsible for operating the instrumentation in the lab to simulate customer-like clinical laboratory. * Maintaining instrument documentation, assist in creation of process and procedures to ensure quality testing data of instrumentation. * Assisting troubleshooting QC and Assay performance data and procedure issues with Management and Assay Lead. Required Knowledge/Skills, Education, And Experience * Bachelor’s degree in medical laboratory science, Biomedical Engineering or other relevant degree required. * 3-5 years of experience in a laboratory/clinical setting. * Strong work ethic, excellent written and verbal communication skills. * Ability to work in a complex, hybrid work environment, remain flexible and agile to switch priorities to meet business needs. * Strong assay and instrumentation troubleshooting skills. * Experience of digital tools including Azure DevOps, Microsoft Office Suite etc. * Experience with Agile software development for medical device products. * Ability to perform instrument qualifications and understand qualification results, including helping other team-members with troubleshooting qualification results. * Experience writing or assisting to write Quality Procedures * Testing experience within a medical device company, experience using Agile software method, preferred. * Experience with Siemens Atellica Solution instrumentation a plus. Who we are : We are a team of more than 73,000 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 Annual Base Pay For This Position Is Min $72,200 - Max $108,300 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. Reasonable Accommodations: Siemens Healthineers is committed to equal employment opportunity. 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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 (https://www.siemens-healthineers.com/careers/recruitment-application-privacy-notice) 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. 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