Artech Information System LLC
Scientist
Artech Information System LLC, Andover, Massachusetts, us, 05544
LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada.Job Description
Responsible for the lifecycle of regulated and clinical samples of biotherapeutics in various matrices to be tested in ligand binding assays on various instrument platforms.Responsible for the routine and non-routine maintenance of lab equipment (e.g. plate washers, plate readers) used in support of regulated and clinical studies.Assist with quality control of operational procedures and software applications in accordance with departmental SOPs and bioanalytical methods.Sample lifecycle management and lab equipment maintenance to be governed per departmental SOP. Attention to detail to ensure accurate execution and documentation of these processes in a regulatory compliant manner.Knowledge of GLP/GCP and working in a regulated environment is highly desirable.Implement various processes needed to manage a sample’s lifecycle which includes accession, check-in and disposal within a laboratory management system (LIMS). Become proficient in LIMS to conduct these activities in a dynamic environment. Collaborate with external groups to resolve sample discrepancies. Assist in the transmission and formatting of clinical files for the importation/exportation of clinical data from LIMS.Execute routine maintenance of lab instrumentation as required per departmental SOPs.
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Responsible for the lifecycle of regulated and clinical samples of biotherapeutics in various matrices to be tested in ligand binding assays on various instrument platforms.Responsible for the routine and non-routine maintenance of lab equipment (e.g. plate washers, plate readers) used in support of regulated and clinical studies.Assist with quality control of operational procedures and software applications in accordance with departmental SOPs and bioanalytical methods.Sample lifecycle management and lab equipment maintenance to be governed per departmental SOP. Attention to detail to ensure accurate execution and documentation of these processes in a regulatory compliant manner.Knowledge of GLP/GCP and working in a regulated environment is highly desirable.Implement various processes needed to manage a sample’s lifecycle which includes accession, check-in and disposal within a laboratory management system (LIMS). Become proficient in LIMS to conduct these activities in a dynamic environment. Collaborate with external groups to resolve sample discrepancies. Assist in the transmission and formatting of clinical files for the importation/exportation of clinical data from LIMS.Execute routine maintenance of lab instrumentation as required per departmental SOPs.
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