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Tasks will include sample extrusion and soil sample processing. Ardaman & Associates, Inc. is one of the largest geotechnical engineering and materials testing consulting firms in the Southeastern U.S. Over our history, we have worked on more than 150,000 projects throughout the Southeast, the U.S., and worldwide.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Responsibilities Perform routine processing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment. Will work in teams and have continual interaction with members of his/her team as well as other sub-teams within QC and QSS, in order to exchange information regarding sample management as it relates to meeting department goals and objectives.
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Manages/performs other aspects of daily lab operations including collections, sample processing, results reporting/distribution, personnel direction (as appropriate), and clerical duties as required to maintain efficient work flow, at a competent level and according to the age/needs of the patient/populations served, communicated special circumstances to appropriate personnel.
Part-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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LabCorp is seeking a dedicated and motivated individual to join their Specimen Processing and Accessioning team in Lowell, MA. The Specimen Accessioner will be responsible for performing clinical specimen accessioning, sample sorting and data entry in a fast-paced, high-throughput environment according to established standard operating procedures.
Part-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Prefer previous experience in a manufacturing environment within pharmaceutical, nutraceutical or food processing industries. Verify there is a LIMS sample number, and reach out to appropriate department if there is none.
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Sample Systems Design and Integration hydrocarbon processing applications - confident with Autocad designing. They will ensure correct designs and bills of material based on customer application and analyzer requirements, along with all relevant electrical and mechanical engineering codes and standards applying to hydrocarbon processing and industrial gas markets.
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The Analytical R&D/Automation Intern will work directly with scientists in the Small Molecule CMC Early Phase Team (Analytical R&D) to develop, optimize, and implement novel automated sample processing workflows using a newly acquired liquid handling system.
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Performing cell culture, flow cytometry sample process and analysis. Processing murine blood and tissue samples. Processing human samples and isolating various lymphocyte and monocyte subsets.
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The duties include specimen procurement and handling, receiving, processing (centrifugation and aliquoting of patient samples), managing sample accountability, answering nursing and provider questions, coordinating specimen drops and patient collections, etc.
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The person in this position interacts with the client, patients, and other PathGroup personnel in a professional and courteous manner and performs with confidence, both the forensic and clinical specimen collection and processing duties following established practices and procedures.
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Responsible for all Sample Processing job skills, including, preparing plasma units for freezing, preparing samples of plasma for testing, and preparing plasma units and samples for shipment.
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6+ years of experience with clinical genomics or bioinformatics, focusing on clinical sample processing, variant curation and interpretation, annotations and diagnostic report generation.
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Stores specimen sample according to required temperature, places samples in appropriate collection container/ tube, accurately labels, follows different procedures as outlined by specific to protocol deemed necessary for transport to maintain integrity of the specimen.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Support trial sample processing, data collection, and data entry of potato and oat trial material both on and off-site including frying, grading, bruising, specific gravity, and assessments.
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May liaise with vendor laboratories, Translational Research lead, pharmacokinetic operations and/or biomarker operations to ensure sample collection, processing, and tracking. Knowledge of Good Clinical Practices ICH/GCP, drug development process, regulatory requirements for the conduct of high-quality clinical trials including protocol development, medical review, oversight of study conduct, data quality and safety is preferred.
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