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As a Systems Design Engineer in our qPCR/dPCR Platform R&D team, you’ll contribute to the development of advanced real‑time and digital PCR systems that help scientists and clinicians uncover insights from genetic information. You will help define, design, integrate, and verify system solutions that connect hardware, software, assays, and algorithms into platforms for life science and diagnostic applications.

• Support the definition of system-level requirements and interfaces for integrated qPCR/dPCR instruments.
• Contribute to architecture discussions and trade‑off analyses balancing performance, manufacturability, and cost.
• Develop and maintain system documentation, design inputs, and requirement traceability in alignment with quality and regulatory standards.

• Conduct hands‑on integration, testing, and resolving problems across hardware, software, and assay subsystems.
• Carry out experiments and verification studies to characterize system performance and identify root causes of issues.
• Apply systems engineering tools and methods (DOE, FMEA, RCA, statistical analysis) to guide design improvements.
• Support prototype build, configuration control, and test data analysis during system development cycles.

• Partner with multi‑functional teams including Mechanical, Electrical, Software, and Assay Engineering to ensure cohesive system functionality.
• Collaborate with Manufacturing, Quality, and Service teams to support design transfer and validation activities.
• Summarize and present test results, analyses, and findings through clear technical documentation and presentations.

• Contribute to model‑based system design and simulation efforts to predict and optimize performance.
• Stay on top of emerging technologies and standard methodologies in systems engineering, instrumentation, and qPCR/dPCR technologies.

• Bachelor’s degree in Engineering (Mechanical, Electrical, Systems, or Software) or Applied Physics with 5+ years of experience developing complex instruments; or
• Master’s/Ph.D. with 0–3 years of proven experience in life science or diagnostic product development.

• Strong, hands‑on background in prototype development, integration, and testing of electro‑mechanical or optical instrumentation.
• Understanding of thermal control systems, fluidics, optics, detection technologies, and signal processing relevant to qPCR/dPCR platforms.
• Familiar with systems engineering processes, from requirements gathering through verification and validation.
• Proficiency with tools such as SolidWorks, MATLAB, LabVIEW, Python, JMP, or similar modeling and analysis software.
• Experience in regulated product development environments (ISO 13485, FDA QSR, CE‑IVD) preferred.

• Highly analytical, meticulous, and data‑driven with strong problem‑solving ability.
• Effective collaborator who builds strong relationships across fields and functions.
• Communicates clearly, both in writing and in technical discussions.
• Self‑motivated and adaptable in a fast‑paced, matrixed R&D environment.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.