Built for laboratory discipline
Make laboratory liquid handling and sample-prep tools that remain explainable under ISO 13485 audit review and under a 2 a.m. STAT sample surge. Since the 1945 Hamburg founding roots through today’s pipette, centrifuge, and incubator platforms, the bar is a filable record—not a slogan.
By 2030, every Eppendorf connected laboratory instrument shipped for regulated environments will carry a clear SBOM path and documented interface expectations where software applies. Near-term milestones (2024–2026) prioritize UDI-ready asset handoffs and ISO 8655 calibration packet formats laboratories can file without retyping.
Working principles
ISO 14971 risk thinking starts with specimen handling, pipette tips, and temperature excursions.
ISO 13485 controls connect design history file (DHF), device master record (DMR), and field actions.
Application specialists translate assay constraints into tip, rotor, and incubator requirements.
Separate FDA cleared, CE IVDR marked, and general laboratory equipment statements by reference.
Calibration and PM evidence must be filable—not just verbally promised.
Community-college and university lab tech pathways feed application support roles.
Cross-functional work
Application Specialist · Pipette Calibration Technician · Field Service Engineer · RA/QA Specialist · Cell Culture Applications
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