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Leads quality assurance for both molecular genetics lab and cytogenetics lab. Oversees quality assurance and regulatory compliance across the laboratory. Coordinates quality assurance for the integration of laboratory information systems.
$176,900 - $228,910 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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d-Matrix has fundamentally changed the physics of memory-compute integration with our digital in-memory compute (DIMC) engine.
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Director, Quality Assurance. Responsibility includes managing supply chain and incoming quality, and in-house manufacturing quality, integrated Supermicro product reliability and performance.
$175,000 - $212,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead CAPA projects (or work closely with Quality Assurance) related to product quality or non-conformities and investigate customer complaints. The Senior QC Scientist is expected to use technical expertise to develop and document quality processes that support the R&D design & development and ensure the reliability and reproducibility of instruments and reagent products.
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Prepare status updates for Manufacturing Readiness Reviews; escalate supplier readiness issues with Quality, Engineering, Commodity Management and Production to determine resolution. Induce supplier activities to strengthen quality systems with FMEA and Error Proofing tools.
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POSITION SUMMARY: The Sr. QA Manager leads a team of Quality Engineer(s), Document Control Specialist(s), and Quality Assurance Specialists. Preferred Education and/or Job experience:Minimum of a Bachelor's degree, preferably in a scientific or technical field, as well as 10+ years direct quality engineering and quality assurance experience within the commercial medical device industry.
$150,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work with manufacturing quality, service engineering, supplier quality, and design teams to identify root causes and drive resolution for failures originating in testing and in the field.
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3-5 years of experience in SMT Quality Assurance Control/Inspection process (PCBA and Electro-Mechanical components) As an SMT Quality Inspection Specialist, you will be part of the Quality Assurance Department supporting the Manufacturing Team. The ideal candidate will have strong attention to detail, excellent communication skills, and a solid understanding of manufacturing processes.
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Our client, a leading manufacturer in the electronics industry, is seeking an SMT Quality Inspection Specialist to join their team. Experience in feeder verification, component ID, verification of polarity, solder joint inspection, missing parts, part value verification using digital meter, etc.
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Trigo’s team of dedicated Delivery Assurance Specialists, Supplier Development Specialists, Supplier Quality Engineers and Program Managers support hundreds of Customers and are deployed to thousands of Suppliers worldwide focused on achieving On-Time and On-Quality Delivery results.
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Lead Incoming Quality Control (IQC) and Outgoing Quality Assurance (OQA) for inspection of incoming parts and outgoing systems to meet quality requirements and specifications.
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The Lead Clinical Lab Scientist performs, as assigned, all technical, analytical, clerical, and quality assurance tasks and duties associated with laboratory testing. Current State of California Department of Health Services Clinical Laboratory Scientist (CLS) License.
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PREFERRED CANDIDATES SPEAKS SPANISH. Skills:Materials Management, Wood manufacturing , Tape Measuring , Blueprint Reading, Microsoft Office, Spanish, Quality Control, MS Office, Blueprints, Quality Assurance, Manufacturing Experience:Entry Level1 year(s) responsibilities: Keeps track of the goods and supplies in a store or warehouse and manages orders to facilitate sales or production.
$23 - $25 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams (process R&D, analytical development, supply chain, quality, clinical, regulatory, DMPK, and tox) to meet CMC and program goals. Thorough understanding and working experience of pharmaceutical drug products concerning GMP, quality systems, ICH guidelines, FDA, EMA, and associated regulatory requirements.
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Quality Assurance Processes and New Product Development approval process APQP/PPAP. Support deployment of policies, procedures, and standards for Supplier Quality Management that meet AS9100 and FAA requirements, including supplier selection and purchase order quality flow down requirements.
$115,260 - $135,600 a yearFull-timeExpandApply NowActive JobUpdated Today
quality assurance jobs Title: supplier quality assurance Company: Pearson in San Jose, CA
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