Cynet systems Inc
Overview
Job Description: Pay Range: $35hr - $40hr Responsibilities And Authorities
The Clinical Laboratory Scientist will play a key role in advancing clinical investigations, conducting laboratory testing, ensuring compliance with quality standards, and supporting product development initiatives. This role requires strong technical expertise in clinical laboratory science, instrumentation, validation, and regulatory compliance. The ideal candidate will demonstrate leadership in scientific projects, contribute to innovation, and provide cross-functional support to ensure accuracy, integrity, and clinical excellence. Responsibilities
Conduct scientific investigations of considerable scope and complexity; explore, identify, and recommend solutions, concepts, and principles. Adapt methodologies as needed to support clinical laboratory operations. Perform clinical testing, maintain laboratory instrumentation, manage reagent test systems, and align laboratory operations with business priorities. Implement and document Quality Assurance (QA) and Quality Control (QC) procedures for instrumentation and methodology. Conduct instrument verification in compliance with CLSI guidelines and assist with procedure updates, instrument performance documentation, and compliance with GLP/GCP. Perform Clinical Software Validations (CSV) and support validation/qualification of new instruments per IQ/OQ/PQ best practices. Stay current in clinical laboratory science through technical literature, continuing education, webinars, and symposia. Train and mentor new laboratory associates on workflow and best practices. Monitor laboratory trends to recommend new projects and influence ongoing initiatives. Contribute to clinical strategy for specimen management products, generating data to support product feasibility and development. Ensure scientific integrity and clinical accuracy in global product claims and communications. Manage individual and complex projects, including multiple internal clinical studies and evaluations. Provide clinical expertise to resolve customer complaints through investigations. Support product innovation, development, testing, manufacturing, and post-market surveillance by collaborating with R&D and Global Clinical Development teams. Knowledge and Skills
Strong working knowledge of clinical laboratory science and practices. Excellent verbal and written communication skills. Awareness or basic knowledge of GCP, GLP, and ISO regulations. Experience with Clinical Software Validations (CSV) and IQ/OQ/PQ instrument validation processes. Phlebotomy experience is a plus. Hands-on experience with human blood specimen collection products. Ability to troubleshoot product and clinical result issues. Strong computer proficiency, including LIS/LIMS systems. Project planning, coordination, and budget management skills. Ability to develop and implement new testing methodologies in collaboration with R&D. Proven understanding of clinical testing areas including blood collection, urinalysis, point-of-care (POC), and laboratory informatics systems. Education and Experience
BS/BA/MA in Clinical Laboratory Science, Medical Technology, Biology, Life Sciences, or a related health field required. MT/MLT CLS (ASCP) certification or equivalent experience in a research or clinical environment. Minimum 5 years of experience in a clinical laboratory environment.
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Job Description: Pay Range: $35hr - $40hr Responsibilities And Authorities
The Clinical Laboratory Scientist will play a key role in advancing clinical investigations, conducting laboratory testing, ensuring compliance with quality standards, and supporting product development initiatives. This role requires strong technical expertise in clinical laboratory science, instrumentation, validation, and regulatory compliance. The ideal candidate will demonstrate leadership in scientific projects, contribute to innovation, and provide cross-functional support to ensure accuracy, integrity, and clinical excellence. Responsibilities
Conduct scientific investigations of considerable scope and complexity; explore, identify, and recommend solutions, concepts, and principles. Adapt methodologies as needed to support clinical laboratory operations. Perform clinical testing, maintain laboratory instrumentation, manage reagent test systems, and align laboratory operations with business priorities. Implement and document Quality Assurance (QA) and Quality Control (QC) procedures for instrumentation and methodology. Conduct instrument verification in compliance with CLSI guidelines and assist with procedure updates, instrument performance documentation, and compliance with GLP/GCP. Perform Clinical Software Validations (CSV) and support validation/qualification of new instruments per IQ/OQ/PQ best practices. Stay current in clinical laboratory science through technical literature, continuing education, webinars, and symposia. Train and mentor new laboratory associates on workflow and best practices. Monitor laboratory trends to recommend new projects and influence ongoing initiatives. Contribute to clinical strategy for specimen management products, generating data to support product feasibility and development. Ensure scientific integrity and clinical accuracy in global product claims and communications. Manage individual and complex projects, including multiple internal clinical studies and evaluations. Provide clinical expertise to resolve customer complaints through investigations. Support product innovation, development, testing, manufacturing, and post-market surveillance by collaborating with R&D and Global Clinical Development teams. Knowledge and Skills
Strong working knowledge of clinical laboratory science and practices. Excellent verbal and written communication skills. Awareness or basic knowledge of GCP, GLP, and ISO regulations. Experience with Clinical Software Validations (CSV) and IQ/OQ/PQ instrument validation processes. Phlebotomy experience is a plus. Hands-on experience with human blood specimen collection products. Ability to troubleshoot product and clinical result issues. Strong computer proficiency, including LIS/LIMS systems. Project planning, coordination, and budget management skills. Ability to develop and implement new testing methodologies in collaboration with R&D. Proven understanding of clinical testing areas including blood collection, urinalysis, point-of-care (POC), and laboratory informatics systems. Education and Experience
BS/BA/MA in Clinical Laboratory Science, Medical Technology, Biology, Life Sciences, or a related health field required. MT/MLT CLS (ASCP) certification or equivalent experience in a research or clinical environment. Minimum 5 years of experience in a clinical laboratory environment.
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