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Reviews Quality Control and determines the acceptability of testing, patient results, and instrument function by applying the principles of QA/QC daily. Integrates various lab processes such as operating instrumentation, resolving customer issues, documenting QC as needed and finalizing results.
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Have experience and/or academic knowledge of Office of Foreign Assets Control (“OFAC”), foreign sanctions such as EU/UN, PEP, Adverse Media, and other AML Watch List types. As a Senior Sanctions QC Specialist, you’ll be responsible for handling quality reviews for sanctions, politically exposed person (PEP) and adverse media (AM)/negative news (NN) alerts, account investigations.
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BS in Biochemistry, molecular / cellular biology or chemistry with a minimum of five years of Quality Control experience in GMP biopharmaceutical or biotechnology industry. This individual will join the Quality Control Bioassay team supporting the GMP manufacturing facilities in Redmond, WA and Seattle, WA. The role is responsible for conducting routine/non-routine testing and analysis of GMP product using methods such as ELISAs, qPCR, and cell-based assays at both Washington state facilities.
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Manage and oversee our cost control and QA/QC program. Experience with project management software such as Prolog, Procore, E-Builder, Bluebeam, Microsoft Project, and Primavera Project Planner (P6.
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The Scientist, QC position supports the Quality Control group at the Rockville GMP facility for IND and Phase I/II GMP manufacturing. Job Title: Scientist I, Quality Control (QC.
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QC Technician II performs daily sampling and testing of manufacturing facilitys water system to ensure it meets regulatory requirements for WFI following established methods and SOPs in accordance with cGMPs.
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The Quality Control Associate performs quality control (QC) functions, including checking pallets for construction integrity, identifying mis-picks and misplaced cases. Complete required level of QC sampling, and required load audit forms.
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Experience in QA/QC or statistical process control. General lab upkeep, some equipment maintenance, and liquid handling QC checks. BS or MS in biology, chemistry, bioengineering, chemical engineering, or related field.
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Independently reviews and records quality control and determines the acceptability of testing, patient results, and instrument function by applying the principles of QA/QC daily. Independently reviews and records quality control and determines the acceptability of testing, patient results, and instrument function by applying the principles of QA/QC daily.
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Checks daily with the Lab Technician and the QC Supervisor to assist with lab testing when compaction tests are not required. Submits daily/weekly core reports to the QC Supervisor, Project Manager and/or Project Engineer in accordance with department procedures.
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Provide Quality Assurance and Quality Control (QA/QC) reviews of technical reports, documents, or proposals prepared by others. In compliance with the Immigration Reform and Control Act of 1986, we will hire only U.S. citizens and aliens lawfully authorized to work in the United States (if the position is or will be one which is subject to U.S. law.
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As our Quality Control Lead you will assist in overseeing QC Technicians to ensure a smooth workflow throughout our QC department. Alerts the QC Supervisor of any unusual or concerning results discovered by the QC Techs; works with the QC and Service Operations Supervisor as well as engineering and manufacturing in assessment and resolution.
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Serve as the authority and lead on matters of instructional design and quality control standards for training content. Our focus is redefining the Government’s relationship with technology by encouraging the use of DevSecOps and Agile methodologies, small-teams constructs, modern tech stacks, and automation.
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Tagged as: ASME, CWI, QA/QC, Quality Control. Development of and providing support with QC packages, procedures, checklists, etc., for all welding, construction, fabrication, inspection, and operation activities.
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The QC Analyst II, position supports the Quality Control group at Rockville Campus. Experience: 2-4 years in the Pharmaceutical or Biotechnology with emphasis in aseptic processing, QC microbiology, environmental monitoring, water system, quality control, validation and manufacturing processes.
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