Senior Staff Scientist - Benchtop Blood Gas Platform (Critical Care R&D)

Senior Staff Scientist, Benchtop Blood Gas – Critical Care Integrate within priority areas of need to assure timely, focused deliverables aligned with strategic direction supporting new product development of electrochemical biosensors/assays. Core Competencies Scientific rigor across all phases of the product development lifecycle. Strong attention to detail and experimental design principles. Proven problem‑solving capabilities with a structured and methodical approach. Extensive chemistry domain knowledge (e.g., electrochemistry, electrochemical sensing, material chemistry). Key Responsibilities Enforce scientific rigor and excellence across all stages of assay/sensor development, ensuring that research outputs are robust, reproducible, and clinically relevant. Drive scientific understanding of assay design by applying fundamental scientific principles and first‑principles thinking to guide innovation, troubleshoot challenges, and optimize performance. Lead the development of novel electrochemical assays and processes for the benchtop blood gas product line with a focus on critical care applications. Resolve complex technical challenges with structured problem‑solving approaches, leveraging Siemens Healthineers tools and processes where applicable. Ensure compliance with regulatory standards and quality systems in all research and development activities. Champion the use of statistical methods and data science practices to enable timely, data‑driven decisions regarding assay design and performance. Mentor and coach junior scientists, fostering a culture of scientific curiosity, innovation, and continuous improvement. Collaborate cross‑functionally with engineering, clinical, quality, marketing and regulatory teams to align scientific strategy with product development goals and patient needs. Required Qualifications MSc or Ph.D. in Chemistry, Electrochemistry, Materials Science or a related field. 10+ years of experience with electrochemical devices and/or sensing technologies. 5+ years working on R&D projects within the medical device industry. Proven track record of successful product development, including product launch, design for manufacturing and technical problem‑solving. Strong understanding of FDA Design Controls, ISO 13485, and ISO 14971. Experience writing design documentation and specifications that meet regulatory requirements. Strong analytical, communication, and project management skills. Ability to work effectively in a dynamic, cross‑disciplinary team environment. Preferred Qualifications Experience with regulatory submissions and compliance. Experience with in‑vitro diagnostic assays. Benefits Medical, dental, and vision insurance; 401(k) retirement plan; life insurance; long‑term and short‑term disability insurance; paid parking/public transportation; paid time off, sick and safe time. Compensation Base pay range: Min $165,490 – Max $248,230. Starting pay may vary by geography, skills, education, experience, and other qualifications. Commission eligibility applies in accordance with the Company’s plan. Commissions are based on individual performance and/or company performance. 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 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 and will provide reasonable accommodations for persons with disabilities. To learn more, 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 View email address on click.appcast.io. 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 U.S. export control law. The Company complies with all U.S. 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 verify any offers of employment on the official Siemens Healthineers career site. Recruitment Agencies Siemens Healthineers does not accept agency resumes. Resumes should not be forwarded to any Siemens Healthineers location. #J-18808-Ljbffr Dormont Manufacturing Co