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The Quality Control Analyst will join our Quality team to be a key player in all scientific and documentation aspects of product development, release, stability, and investigations in support of maintaining and improving processes within the CRISPRevolution Production Team.
$30 - $34 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Accredited training in service advisor skills, customer satisfaction, and quality control. A team player who is focused on providing exemplary customer service. Swickard has positioned itself as a leader in highline brands such as Mercedes Benz, Toyota, Lexus, Porsche, Audi, and Jaguar-Land Rover among others.
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Within the Facilities Division of the Public Works Department, electricians perform a variety of skilled and technically complex tasks in the operation and maintenance of City facilities with essential functions that include installing, troubleshooting, repairing, and maintaining building electrical distribution systems, lighting fixtures, lighting control systems, motors, VFDs, EV chargers, generators, and transfer switches.
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Expand your knowledge of machine learning vision systems and capabilities for manufacturing quality control. As a Battery Hardware Technician, you'll:Guide installation and acceptance testing of new manufacturing quality sensing systems.
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Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.
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Provide required support to Quality, Production and Field Service team as the control boxes moves along the production until completion and any on-site issues. Design and draft control drawings that is in line to customer specification, industry standards and company standards considering the best, optimized approach in terms of cost and quality.
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In this position, you will work closely with the Process Development, Quality Control, Analytical Operations, Quality Assurance, Translational Medicine, Biometrics, and Regulatory team members and will contribute to flow cytometry-based assay development for product understanding of CARGO Therapeutics' pipeline candidates, method transfer and/or qualification, SOP/technical report authoring and review, method life cycle management, data analysis, and execution of routine analytical testing.
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As a Senior Software Quality Engineer in the Alluxio QA team, you will be responsible for various aspects of delivering the Alluxio project as a product into the hands of our users. 1+ years of relevant experience in Quality Engineering, specifically Automation Testing, Test Framework development.
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In this role, you will:Develop schematics comprised of FPGAs, SoCs, memories, communications devices, analog devices, ADCs, DACs, motion control devices, feedback sensors, power supplies. Aid layout designers in the layout process, applying your skills to achieve optimal placement, routing, PCB stackup, signal quality, manufacturability, and cost.
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You would also be in charge of processing damaged or defective products back to the Fulfillment Center, and reporting these items to the Inventory Control Team. Additionally, you would be responsible for providing every customer with a great experience.
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Provides guidance and direction to staff, enabling the accurate, timely and efficient completion of instrument maintenance, quality control, non-conforming event management and records management.
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As a compute & control systems engineer in Advanced Hardware Engineering (AHE), you will be responsible for developing and documenting component requirements for compute and control modules.
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Under supervision, assists certificated SLPs or other professional staff in providing a variety of speech therapy services to special education students in accordance with IEP goals; provides therapeutic remediation in speech and language skills to students with special needs, including activities designed to develop pre-language and language skills and oral-motor control for speech production and vocalization; and related work as required.
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Monitor, track, and trend stability data and GMP quality systems and establish metrics. Develop, implement, and maintain GMP quality management systems, policies, and SOP. Experience in Device Quality System, Design, Manufacturing and Testing, 21 CFR Part 820, DHF, DHR, DMR, and overall Device Regulations, CDRH and 510 k or PMA approvals are a plus.
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Demonstrated knowledge and technical competence in routine specimen collection, preparation, testing applications, laboratory operations, and quality assurance in one or more assigned clinical specialty areas; examples: Chemistry, Special Chemistry, Hematology/Coagulation, Urinalysis and Transfusion Service.
$71.2 - $88.98 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago
quality control jobs Title: team lead Company: Comoto in Redwood City, CA
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