Kellie Jacobs Email & Phone Number

Basel, Baselstadt, Ch

-administration of QC in-process, release, and stability samples, associated document coordination, and collection of data-input, review, and approve QC test results in LIMS- adhere to all GMP requirements, including FDA/EMEA regulations-Coordination with quality management to support investigations- May support management with activities related to training of employees, GMP compliance, and identifying and implementing CAPA

Chicago, Il, Us

Work with a cutting-edge genomics workflow to provide high-quality next-generation sequencing data with rapid turnaround times in a clinical laboratory.Perform routine testing, quality control, calibration, maintenance and proficiency testing in accordance with current laboratory procedures.Perform complex molecular-based procedures with a high degree of quality and in accordance with established protocols.Create plate maps and program files as required for normalization and hybridization pool processesPerform next-generation sequencing, including nucleic acid extraction, DNA/RNA quantification and qualification, NGS library preparation, probe hybridization, probe/library capture, library cleanup and quantification, loading sequencing libraries onto the Illumina Novaseq.Sterilizing laboratory equipment and workspaces as assigned.Entering clinical patient data into the Laboratory Information Management system.Obtain 12 continuing education hours in the field of oncology or molecular biology.Maintain competency to perform all assigned molecular biology protocols in accordance with CAP, CLIA, NYSDOH regulations.

Durham, North Carolina, Us

Durham, North Carolina, Us

- Perform duties as dictated by standard operating procedures (SOPs) for cell manufacturing and under G'X'P (GLP,GTP, GMP) guidelines as directed.- Perform duties in a clean room environment following GMP guidelines.Operate instrumentation as needed for cell manufacturing such as cell processing systems (Lovo) and bioreactors (Quantum) Use aseptic technique to manufacture cell products for clinical trials Operate manual and automatic laboratory equipment to count cells; stain cells, wash cells,identify and quantify cell populations including stem cells.- Perform environmental monitoring for the GMP laboratory Assist in technology transfer of procedures from pre-clinical into GMP environment Write SOPs, and batch records as requiredUtilize MasterControl System to update documentation as neededWork with Quality Assurance to prepare Deviation Reports as neededWork with Lab manager and quality assurance to ensure the facility is in compliance for governing regulations Participate in lab inspections and work with inspectors as needed- Maintain sufficient inventory of supplies and reagents for performance of duties; clean and maintain laboratory equipment in good working order.Coordinate and participate in the preparation of antibodies, reagents, and solutions necessary for cell processing and testing.

Burlington, North Carolina, Us

Perform maintenance on centrifuges and Tecan Freedom Evo robots as requiredRun Illumina Infinium assay in a high-throughput laboratory environment according to Standard Operating ProceduresPerform DNA extraction and quantification using Tecan Freedom EvoPerform DNA amplification via whole-genome amplification techniqueComplete paperwork in accordance with Good Documentation Practice standardsCross-train with Molecular Microbiology laboratory in the use of Magna Pure 96 extraction and Biofire assays

Costa Mesa, California, Us

Preparing necessary supplies as neededCounting down cash registerAssisting customers with selectionsPreparing beverages according to standard procedures

Raleigh, Nc, Us