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Common tasks involve review of Software Release Packages (PDM, ADS), CDRL Deliverables (IR, CN, ECP), Software Investigation Requests (SIRs), Software Trouble Reports (STRs, Code Reviews), Physical Media (Loader Verifier), Test Artifacts, as well as participation with Peer Reviews (SW, SE), Control Boards (SRB, SSRB), Tracking Books (Metrics Monitoring), Command Media (Policies & Procedures), Test Witnessing (SQT, FQT), and Audits.
$96,000 - $200,000 a yearFull-timeExpandUpdated 12 days ago - UpvoteDownvoteShare Job
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Familiarity with PTC MathCAD software Previous Quality Assurance/Quality Control experience Periodic travel may be required. Experience implementing control and protection schemes including interpreting schematics and wiring diagrams and preparing relay logic to complete the schemes.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Performs a variety of point of care testing functions and quality control such as urinalysis, rapid strep, blood glucose, urine pregnancy, etc. Join a community-based, multi-specialty, physician-led organization where you will work with talented peers on a common purpose: improving the quality, cost and experience of health care.
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Must demonstrate ability to learn and independently operate equipment such as pumps, engines, centrifuge, generators, valves, gates, mixers, conveyors, blowers, dryers, chemical feed, odor control, disinfection equipment, sludge processing filters, belt presses and measuring/control devices, testing equipment and material handling equipment.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Proclinical is seeking a dedicated and innovative Site Microbiologist to act as a technical lead for Quality Control (QC) Microbiology programs in a dynamic biopharmaceutical manufacturing environment.
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Performs equipment quality control, transporting of patients and room set up and clean up. TRA Ultrasound Technologist or Sonographer performs all General Ultrasound Imaging exams utilizing proper technique, processes correctly marked images, calibrates and operates ultrasound equipment, completes computerized tracking and supply charges, and assists Radiologist during invasive exams.
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As the Quality Assurance Lead, you must possess a strong background in Quality Systems, Document Control, Supplier Quality, and Validation within the biotech industry. Demonstrated experience with Quality Systems, Document Control, Supplier Quality, and validation activities.
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Location: Reliant Medical Group, a Part of Optum: 900 Union St. Westborough, MA. Opportunities with Reliant Medical Group , part of the Optum family of businesses. Join a team at the forefront of value-based care and discover the meaning behind Caring.
Part-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Assure Wyman-Gordon's Quality systems and procedures satisfy government and customer requirements, and assure compliance of product shipped to contractual requirements. This position requires use of information or access to production processes subject to national security controls under U.S. export control laws and regulations (including, but not limited to the International Traffic in Arms Regulations (ITAR) and the Export Administration Regulations (EAR.
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This position indirectly supports ongoing manufacture of biological clinical trial materials by providing timely and compliant support for quality systems including Change Control administration, Calibration / Validation review, MasterControl system administration and workflow development, inspection management and hosting, internal auditing, supplier management, site Quality Council, quality metrics generation, and site-level compliance deliverables.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Common SWQE tasks involve review of SW Release Packages (Windchill PDM, Azure DevOps Server), CDRL Deliverables (IR, CN, ECP), SW Investigation Requests (SIRs), SW Trouble Reports (STRs, Code Reviews), Physical Media (Loader Verifier), Test Artifacts, and participation in Peer Reviews (SW, SE), Control Boards (SRB, SSRB), Tracking Books (Metrics Monitoring), Command Media (Policies), Test Witnessing (SQT, FQT), Audits.
$96,000 - $200,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform/Ensure company's Quality Assurance/Quality Control (QA/QC) processes are being follow on all design packages. Typical design to include general arrangement, equipment and electrical layout, elevation views, cable trench, grounding, conduit drawings, details, bills of material, and AC and DC power systems.
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Responsible for end-to-end Quality within the site, including FUSE qualification/validation, materials management, batch record reviews, change control, CAPA plans and deviations. Work closely with Quality Systems and Compliance, and External Quality Operations to advance all aspects of CRISPR’s GMP Quality processes.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The QC Analyst II is responsible for executing quality control analytical tasks, including in process manufacturing testing, for one or more projects to support testing and release of oligonucleotides.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Astellas is announcing a QC Analyst I Microbiology opportunity at their Astellas Institute for Regenerative Medicine (AIRM) site in Westborough, MA. Purpose:AIRM is seeking a highly motivated individual to join us as a QC Microbiology Associate I. This position provides Quality Control Microbiology support to all aspects of a GMP environmental monitoring program and product testing.
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