Technical Specialist - KRYPTOR Systems and Assays

Work Schedule Flex Shifts 40 hrs/wk Environmental Conditions Office Job Description Thermo Fisher Scientific’s Clinical Diagnostics business is committed to enabling customers to improve patient care through innovative diagnostic technologies and scientific partnership. Within Medical Affairs, this role supports the B·R·A·H·M·S KRYPTOR compact plus and KRYPTOR gold platforms and the associated assay menu used across clinical and research settings. This field-facing technical specialist role serves as a key laboratory and scientific resource for internal teams and external customers combining scientific education, technical consultation, assay implementation, validation support, troubleshooting, and customer enablement activities across both clinical and research environments. Discover Impactful Work As a Technical Specialist – KRYPTOR Systems and Assays, you will play a critical role in supporting customers and internal partners with deep technical and laboratory expertise related to the KRYPTOR compact plus, KRYPTOR gold, and associated assays. You will provide education and guidance across the customer journey, from pre-installation planning and assay implementation through validation, training, troubleshooting, and ongoing scientific support. A day in the Life Serve as the primary laboratory and technical specialist within Medical Affairs for the KRYPTOR compact plus, KRYPTOR gold, and related assay portfolio. Provide customer-facing technical education on instrument operation, assay workflow, implementation considerations, validation planning, and best practices for use in clinical and research environments. Support customer and/or study site onboarding and implementation activities, including workflow discussions, assay setup, operator education, and coordination with internal technical and commercial teams. Guide laboratories and research customers through assay verification and validation processes, helping them understand performance characteristics, workflow requirements, documentation expectations, and operational considerations. Provide ongoing post-implementation support to study sites and customers, including utilization and workflow assessments, process optimization, best practice sharing, refresher training, and coordination of preventive maintenance activities. Provide hands‑on testing support and technical expertise for research projects, collaborative studies, and assay‑related investigations. Support reagent forecasting, inventory planning, and supply coordination activities to ensure continuity of operations for study sites and research customers. Act as a scientific and technical partner for commercial teams in customer discussions involving KRYPTOR systems, assay applications, implementation planning, and post‑installation success. Support both commercial and research opportunities by participating in customer calls, presentations, and technical discussions related to KRYPTOR platform capabilities and assay use. Provide technical troubleshooting and escalation support for customer and study site inquiries, collaborating with technical support, product support, field service, and global teams as needed, including participation in customer complaint investigations and field service interventions. Develop and deliver virtual and in‑person training materials, presentations, and educational programs for laboratorians, researchers, and internal colleagues. Collaborate with Medical Affairs and Commercial leadership to identify customer needs, support assay adoption, and strengthen customer experience. Serve as an internal subject matter expert on KRYPTOR workflow, assay applications, and laboratory implementation considerations. Collect and communicate field insights, customer feedback, and unmet needs to internal stakeholders to help inform training, messaging, product support, and strategy. Represent Thermo Fisher Scientific at customer meetings, workshops, congresses, advisory boards, and scientific events as appropriate. Ensure all activities, training, and discussions are conducted in accordance with applicable healthcare compliance requirements and approved use parameters. Keys to Success Education Bachelor’s degree required in medical technology, clinical laboratory science, biology, biochemistry, immunology, or related life science field. Advanced degree preferred. MT/MLS/ASCP or equivalent clinical laboratory certification preferred. Experience 5+ years of experience in a clinical laboratory, diagnostics, medical device, or life sciences environment. Hands‑on experience with immunoassay systems, automated analyzers, or related laboratory instrumentation required. Experience leading and/or coordinating laboratory instrument implementations, training, assay validation, troubleshooting, or workflow change/optimization initiatives strongly preferred. Customer‑facing experience in technical support, applications, field training, medical affairs, or scientific affairs preferred. Demonstrated ability to build trusted relationships with laboratory leaders, technical staff and other key personnel in supporting both clinical and research customers is highly desirable. Experience working cross‑functionally with sales, marketing, service, technical support, and global partners preferred. Prior experience as a Medical Technologist, Medical Laboratory Scientist, Clinical Laboratory Scientist, Technical Supervisor, Laboratory Educator, or Field Applications Specialist strongly preferred. Knowledge, Skills, Abilities Strong technical knowledge of automated immunoassay systems and clinical laboratory operations, including Time‑Resolved Amplified Cryptate Emission (TRACE) technology. Ability to understand and explain assay principles, instrument workflow, quality practices, and validation concepts to laboratory and research audiences. Strong presentation and training skills, with the ability to tailor content to laboratorians, researchers, and internal stakeholders. Excellent verbal and written communication skills. Solid Understanding of laboratory quality systems, including QC, proficiency testing, CAP standards, CLIA requirements, and laboratory inspection readiness. Ability to review and interpret assay performance data, including precision, linearity, method comparisons, reference intervals, QC trends, and troubleshooting results. Familiarity with LIS, middleware, analyzer interfaces, and laboratory workflow integration preferred. Experience investigating technical issues, identifying root causes, and supporting corrective actions for laboratory or instrument‑related problems. Ability to work independently in a field‑based or highly matrixed environment. High level of organization, time management, and attention to detail. Proficiency in Microsoft Office applications. Experience using CRM systems and documenting customer interactions, training activities and technical support cases preferred. Willingness and ability to travel domestically up to 75% with occasional travel internationally. Must be able to lift, carry, and transport materials, and training supplies weighing up to 25 pounds. 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. #J-18808-Ljbffr ThermoFisher Scientific