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The QC Data Manger will be responsible for overseeing review for accuracy and interpretation of data generated internally from testing laboratory charged with the execution of all GMP bioassay and Nucleic Acids Testing (release and stability) related to Sarepta’s Gene Therapy pipeline.
$112,000 - $140,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our offerings include source testing for routine regulatory compliance, engineering studies, control device evaluations, MACT demonstrations, relative accuracy test audits (RATAs), and trial burns; ambient air monitoring; temporary continuous emissions monitoring systems (CEMS); and advanced testing capabilities in Fourier Transform Infrared Spectroscopy (FTIR) and gas chromatography.
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Robust background in adhering to GLP and cGMP standards, along with hands-on experience in assay development and validation, is obligatory. is seeking a talented Senior Scientist I to join our Bioanalytical Laboratory team in Woburn, MA. As a key member of the team, you will lead the development and validation of new assays, including GxP assays.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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QSA Global, Inc. specializes in supplying state of the art gamma radiography and portable X-ray systems used in non-destructive testing (NDT) as well as high-performance radiation sources used in oil well logging (OWL), industrial processes, and nuclear medicine.
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Proven laboratory expertise in radioactive product development or manufacturing, radiochemistry, including radiochemical separations and chemical synthesis. Uphold laboratory standards by assisting in the training, development, and mentoring of staff, and maintaining rigorous laboratory procedures.
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Coordinate the environmental testing of hardware including: vibration, shock, thermal, fatigue, and others as required. Coordinate the fabrication and environmental testing of design hardware.
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Proven experience with all phases of automation projects including conceptual, basis of design, implementation, testing, start-up and commissioning of Process Control System (PCS), SCADA, and DCS in the Life Science industry.
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The following procedures can be completed by the nursing associate once competency training is completed: bladder scan, point of care blood glucose testing, point of care fecal occult blood testing, use of tonsil tip for oral suctioning.
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Fully characterize coin and pouch cell performance using new materials and formulations utilizing electrochemical testing and analytical techniques to understand reaction mechanisms, failure modes, and potential benefits.
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The individual will also assist in managing quality events, data trending, and review of quality documents originated at the testing laboratory at Sarepta. The incumbent will be involved in the design and execution of novel cell-based assays, writing technical reports, supporting method validation and qualification activities performed in the Sarepta Gene Therapy QC laboratories and/or at contract testing laboratories.
$96,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The ideal candidate will have a broad understanding of semiconductor tools, processing techniques, microelectronic circuit testing, and circuit design with individual expertise in one or more of these areas.
$77,000 - $163,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The projects this person will be working on will require them to use the OpenEdge Advanced Business Language (ABL) and SQL clients in testing new Database functionality. Perform product regression testing of software prior to product releases.
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Lead investigations into significant quality issues, scientific misconduct and suspected serious breach of GCP or GLP; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities, as appropriate.
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The Senior Controls Engineer will interact directly with the customer and lead a team of engineers in identifying requirements, developing specifications, and implementing/testing/commissioning/qualifying automation solutions.
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Experience in GLP toxicity studies in both small and large animal models. 12 peer reviewed publications in pharmacology, toxicology, or relevant biomedical science discipline. Diplomate of American Board of Toxicology (DABT) required for Sr. Principal Toxicologist.
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glp testing jobs Title: laboratory assistant in Wilmington, MA
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