Human Relevant Models – Applications Scientist at Danaher · San Jose

Human Relevant Models – Applications Scientist Location: San Jose, California, United States Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Molecular Devices, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Join Molecular Devices and help drive scientific discovery for life science customers in academia, biotech, pharma, and government. Our automated and AI-enabled technology empowers researchers to tackle complex questions and gain deep insights, accelerating the development of safer, more effective therapeutics. As part of our team—rooted in collaboration, authenticity, and innovation—you’ll ultimately contribute to groundbreaking science that enhances lives globally and shapes a healthier future for all. Learn about the Danaher Business System which makes everything possible. The Human Relevant Models – Applications Scientist is responsible for executing robust biological application and validation studies using organoid and other human‑relevant model systems, with a strong focus on reproducibility, process discipline, and quality. The role applies a manufacturing‑ and quality‑oriented mindset to experimental execution, ensuring data, workflows, and documentation are reliable, scalable, and fit for intended use This position reports to the Manager – Science and Validation and is part of the Product Innovation and Strategy Team located in San Jose, California and will be an on-site role. In this role, you will have the opportunity to: Execute application and validation studies for human‑relevant models Design, run, and deliver high‑quality experimental work using organoids and advanced cell models to support product validation, workflow verification, and defined project milestones. Develop, qualify, and characterize organoid and complex cell models Establish, optimize, and characterize organoid and human‑relevant model systems to ensure robustness, reproducibility, and fitness for validation and workflow use. Analyze, interpret, and communicate scientific data Document, analyze, and interpret experimental data; prepare clear technical summaries, figures, and reports for internal review and decision‑making, and for external stakeholders where required. Maintain quality, compliance, and documentation standards Ensure experimental, validation, and project documentation is complete, accurate, and compliant with applicable quality, safety, and regulatory expectations; actively contribute to raising scientific and quality standards. Identify risks, troubleshoot issues, and improve workflows Proactively identify technical and experimental risks, troubleshoot issues as they arise, implement mitigation strategies, and contribute to continuous improvement of organoid and human‑relevant model workflows. The essential requirements of the job include: Qualifications in a relevant life‑science discipline PhD in biomedical sciences or a related scientific field or a BSc in a biomedical or related discipline with 2+ years of relevant industry experience. Strong hands‑on experience in mammalian cell biology Significant practical experience with mammalian cell culture techniques is essential, with experience in complex models such as complex cell cultures, stem cells or organoids critical. Ability to independently plan and execute experimental work Demonstrated ability to plan, prioritize, and execute experiments independently, delivering high‑quality scientific outputs to defined milestones and timelines. Proven data analysis, documentation, and reporting capability Experience documenting, collating, analyzing, and interpreting experimental data, with strong record‑keeping and the ability to communicate results clearly to internal and external stakeholders. Experience working with quality, compliance, and experimental discipline Experience maintaining accurate documentation and working to defined quality and safety standards. Travel, Motor Vehicle Record & Physical/Environment Requirements: Occasional travel may be required to support project needs, including visits to other Molecular Devices sites, customer or collaborator locations, and attendance at scientific meetings or conferences. No routine driving or company vehicle use is expected. This role is primarily laboratory‑ and desk‑based. Ability to work for extended periods in a laboratory environment, including: Standing for prolonged periods Manual handling of laboratory equipment and consumables Must be able to work safely in accordance with health, safety, and biosafety procedures at all times. Use of appropriate personal protective equipment (PPE) is required. It would be a plus if you also possess previous experience in: Experience in regulated or GxP‑aligned environment. Experience working in milestone‑driven, project‑based scientific environments Prior experience delivering scientific work against defined project plans, timelines, and technical milestones. Molecular Devices, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. The annual salary range for this role is $83,000 - $120,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.