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Maintains quality assurance requirements and manages field inspection and monitoring code compliance issues. The Mechanical / Electrical / Plumbing (MEP) Inspector will support a variety of MEP construction projects that may include water/wastewater, chemical or manufacturing including piping, equipment and instrumentation construction; electrical power distribution systems conduit and wiring; voice/tele/data systems; instrumentation and control systems; plumbing; HVAC installation and commissioning of Plant systems.
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Minimum 3 years of experience in Quality, Supplier Quality, or Manufacturing, in the automotive, aviation, or medical device industries or a combination of both Supplier Quality and Internal Plant quality development.
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Drive continuous improvement throughout the supply base using quality and lean manufacturing tools. Provide support to Manufacturing, Quality, and Vehicle Engineering regarding analysis and disposition of suspect supplier material.
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Requirements:Candidates with experience in Automotive manufacturing processes such as plastic injection molding (highly preferred), metal stampings, machining, assembly, paint etc. Candidates with experience in Automotive manufacturing processes such as plastic injection molding ( highly preferred), metal stampings, machining, assembly and paint will be highly preferred.
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Must have experience with Automotive manufacturing quality processes including plastic injection molding, metal stamping, machining, assembly and/or paint application. As a Supplier Quality Engineer, you will be part of the Quality Team supporting Manufacturing.
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Proven track record of successfully leading quality assurance teams and driving continuous improvement initiatives in a pharmaceutical manufacturing environment. Collaborate with cross-functional teams, including Research & Development (e.g. clinical development, clinical operations), manufacturing, supply chain, and regulatory affairs, to ensure alignment and integration of quality assurance processes throughout the product lifecycle.
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As a PCBA Manufacturing Engineer, you will work across design engineering, supply-chain, quality, and our manufacturing partners to drive electrical sub-system and PCBA manufacturing and delivery.
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The successful candidate will have some knowledge and engage in analytical LC/MS/MS method development, validation, and the assaying of clinical samples in compliance with the Food and Drug Administration's (FDA's) Good Laboratory Practice (GLP) and National Institute of Health's (NIH's Division of AIDS' (DAIDS) Clinical Pharmacology Quality Assurance (CPQA) regulatory guidelines (DAIDS) Clinical Pharmacology Quality Assurance (CPQA) regulatory guidelines.
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Design and implement manufacturing and assembly processes for new products and optimize existing processes to increase efficiency, reduce cost, and ensure quality. Are experienced working with a variety of manufacturing processes (injection molding, machining, sheet metal, printing, casting, extrusions, SMT electronics, additive manufacturing, finishing processes, etc.
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PhD in Biochemistry, Molecular Biology, Biology or related subject with 0-5 years of analytical experience in the cell and gene therapy manufacturing field. BS in Biochemistry, Molecular Biology, Biology or related subject with 10-15 years of analytical experience in the cell and gene therapy manufacturing field OR.
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The Supplier Quality Engineers work alongside Supplier Development Engineers and the team reports through to our Supplier Quality Engineer Manager. We have multiple Supplier Quality Engineer positions available and will be considering applicants from a mechanical or electrical background.
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Working closely with our stellar Manufacturing, Quality, and Compute teams, you will be working hands on in the front lines of production, while helping to continuously improve our cutting edge bioprocess from the ground up.
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In this role, you'll have the opportunity to work on the electro-mechanical assembly for our AUV, including manufacturing, assembly, testing, and quality control. Experience with quality control and documentation procedures.
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Minimum of 2 years experience in a GMP Quality Assurance role. Main Purpose of the Position Provide quality expertise and compliance oversight for GMP suppliers such as Contract Development Manufacturing Organizations CDMOs and Contract Research Organizations CROs for the delivery of products including bulk drug substance bulk drug product and finished goods Serve as the Quality Point of Contact for designated GMP suppliers and products.
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Be responsible for menu compliance, cooking, food production, food quality/presentation, safety/sanitation; ensure Sodexo culinary standards and food quality are implemented.
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food manufacturing quality assurance jobs in South San Francisco, CA
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