New 
Scientist, Sample Management and Sample Processing
 Spectraforce Technologies | |
 United States, Illinois, North Chicago | |
 Jan 23, 2026 | |
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Job title: Scientist, Sample Management and Sample Processing
Location: Onsite - Lake County, North Chicago, IL; 60064 6 months to start Purpose: The Genomics Research Center (GRC) is part of the Quantitative Medicine and Genomics (QM&G) functional area that promotes data-driven innovation in drug discovery by integrating diverse quantitative data and leveraging advanced computational models. The GRC's goal is to develop world class genetics and genomics research focused on finding the right therapeutic targets and helping scientists better understand not only human disease biology but also the behavior and response to our drugs in clinical trials across all therapeutic areas. Join our innovative Genomic Technologies (GTECH) lab team, where we are at the forefront of genomic research and discovery. Our team is dedicated to advancing science through cutting-edge technologies and collaborative efforts. We are seeking an experienced and highly organized Sample Management and Processing Scientist (I) to support impactful reverse translation focused projects. In this role, daily responsibilities will center on supporting gDNA isolation from clinical samples across multiple therapeutic areas. The Scientist (I) will execute manual and automated workflows for high-quality nucleic acid extraction, perform rigorous quality control assessments on isolated nucleic materials, maintain detailed and accurate documentation in LIMS, and interpret and report QC data. In addition, effective cross-functional communication with researchers is essential to ensure the integrity and utility of isolated gDNA for downstream analyses. The successful candidate should have hands-on expertise with diverse nucleic acid extraction methodologies, meticulous adherence to SOPs, and a solid understanding of sample biology as it relates to clinical research. Operational excellence, attention to detail, and organizational skills will be critical to deliver reliable support for reverse translation clinical initiatives. Responsibilities: * Adhere to department generated and company standard operating procedures for communication, lab operations, project reporting, and lab safety. * Perform nucleic acid extraction, quality control, and interpretation of data with minimal supervision and aligned to delivery within project timelines. * Attain operational proficiency for required daily functions within training schedules. * Perform troubleshooting for wet lab tasks independently and with collaboration. * Maintain clear and accurate documentation of all processes. * Formally and informally communicate project progress, completion, and data by delivering reports through collaborative meetings, and verbal or written presentations. * Timely recording and documentation of wet lab processes and progress in applicable LIMS and project management applications in accordance with policies and procedures. * Support the development and testing of LIMS workflows. * Maintain instrumentation as outlined by laboratory standards and manuals. Qualifications * Experience required. BS degree in Genetics/genomic or related field or equivalent with 4+ years relevant experience, MS degree in Genetics/Genomics with 2+ years relevant experience. * Theoretical and practical knowledge to carry out job function including but not limited to: o Experience with performing routine and or complex nucleic acid workflows from source material such as cells, tissues, blood, other biofluids. o Experience with performing routine and/or complex nucleic acid quality control and analyzing/interpreting data including but not limited to fluorescence quantification, absorbance, and integrity analysis. o Experience with sample processing from source materials to nucleic acids within a laboratory management system. o Proficiency in micropipetting and wet lab automation for multiple genomic laboratory techniques. o Ability to strictly adhere to SOPs and lab guidelines and thoroughly report deviations in a timely manner. o Strong computer skills, especially in Microsoft Office Suite. o Self-directed to deliver timely results both independently and collaboratively in a fast-paced and fluid environment with high attention to detail. o Strategic project planning and critical thinking to resolve routine and complex problems. Preferred * Experience with low and high throughput sample tracking and data management (LIMS). * Experience with performing and maintaining workflows on automation platforms. * Experience in a CLIA certified laboratory or other regulated laboratory environments. * Experience in clinical writing and editing documents/manuals. * Works well in a multidisciplinary team environment. * Capacity to learn new methodologies/techniques quickly and drives innovation to improve workflows. * Demonstrates effective and efficient communication. | |