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If RRT, required to obtain RPSGT or Sleep Disorder Specialty (RRT-SDS) credential within 2 years of starting. Responsible for performing sleep study procedures and may perform neurodiagnostic testing for applicable patient populations.
$24 - $36 an hourPart-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Discusses reasons for performing laboratory testing and complete blood draw using vacuum tube system, butterfly, and capillary puncture. Administers a 12-lead electrocardiogram and describe importance of Clinical Laboratory Improvement Amendments (CLIA), Occupational Safety and Health Administration (OSHA), and Safety Data Sheets (SDS) in the healthcare setting.
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Experience with ELISA, SDS-PAGE, and electrophoresis. The QA Scientist I will be responsible for performing release and stability testing on donor screening products. The QC Serologist I will perform testing within established timelines in accordance with current cGMP's.
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KTAs hallmark services include coatings failure analysis, forensic laboratory investigations, and independent laboratory testing of coatings performance, among a much broader array of integrated service offerings.
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Preferred: Registered Polysomnographic Technologist (RPSGT), Register Sleep Technologist (RST) or NBRC Sleep DIsorder Specialist (SDS) or Registered Respiratory Therapist. Reviews existing information in the patient record, examines orders and protocols for study, recognizes sleep/wake or respiratory complaints, sleep patterns and potential need for treatment intervention during testing, collects pertinent patient information to insure proper interpretation by the physician and communicates with ordering physician or center/lab director to clarify unclear or inappropriate orders and communicates information about the patient's status.
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Additional related education and/or experience preferred, including PFT, SDS, NPS, NRP, ACCS and/or AE-C. This position independently provides respiratory care, pulmonary and cardiology diagnostic testing to patients in a variety of health care settings.
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Ability to identify cleaning and chemical supplies, ability to read and understand Hazard Communication Safety Data Sheets (SDS), ability to understand proper applications of chemicals and general cleaning supplies and ability to frequently handle these products.
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Extensive expertise in U/HPLC, CE, SDS-PAGE, mass spectrometry, and other analytical technologies as applied to protein analytical method development, trouble shooting and validation for GMP release and stability testing.
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The position is responsible for analytical development, analytical technology transfer and validation, and overall management of CMC activities related to external QC testing/release and stability of antibody drug conjugates and intermediates.
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The successful candidate will have hands-on experience with cell-based in-vitro potency assays, SDS-PAGE, Automated Western blot assays, enzyme activity measurements, protein extraction, purification, and quantification methods.
$72,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience in laboratory testing such as: SEC UHPLC, Potency and Residual Protein (ELISA), Osmolality, Solo VPE, Capillary Electrophoresis (SDS/rCE-SDS), Assay (icIEF), This position will be responsible to support the QC Lab Operation activities regarding documentation approval, initial deviation investigation, environmental monitoring, and testing to ensure compliance with all regulatory requirements, company policies, values, and goals.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays.
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Complies with OSHA/British Columbia Workers Compensation Act and Occupational Health and Safety Regulation requirements and Risk Management programs and policies, adheres to safety rules and regulations, and practices safety procedures at all times including Personal Protective Equipment (PPE), fire extinguishers, Safety Data Sheets (SDS), and Lockout Tagout procedures.
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HPLC, ELISA, SDS-Page, Gel Electrophoresis experience preferred. The Quality Control (QC) team is responsible for testing products, raw materials and the manufacturing environment to ensure the Safety, Quality, Identity, Purity and Potency produced by the Catalent Madison Biologics facility.
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The Research Associate II, Analytical Testing, will be responsible for performing various analytical assays, including but not limited to ddPCR, RT-qPCR, ELISA, enzymatic assays, and cell-based assays, to characterize several gene therapy vectors.
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