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Develop, lead, direct, update, reassessment, verification and periodic validation of FSQA programs including HACCP Program, Sanitation Standard Operating Procedures, Pest Control, Good Manufacturing Practices, Approved Supplier Program, Foreign Material Control, Plant Sanitation, Chemical Control, Product Quality Assurance, FSQA Customer Complaints, Food Defense and Security.
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10+ years’ experience in process engineering or product quality assurance for electronics or mechanical product. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
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Align Quality Management System where it utilizes Advance Product Quality Planning (APQP) and subsets including; Production Part Approval Process (PPAP), Controls Plans, Failure Mode and Effect Analysis (FMEA), SPC, 6S, Lean, and Supplier Quality Assurance (SQA) processes.
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Development of quality process links with customers in line with the QMS, PPAP, APQP, Controls Plans, FMEA and Supplier Quality Assurance processes. Advanced Product Quality Planning (APQP), Controls Plans, Failure Mode and Effect Analysis (FMEA) and Supplier Quality Assurance (SQA) processes and oversee continued compliance and embedding across the business.
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Basic Quality Engineering responsibilities: (AS9145) Process Flow Diagram (PFD) Process Failure Mode and Effects Analysis (PFMEA) Control Plans (CP) Measurement System Analysis (MSA) (Gage R&R) Internal Audits (Quality Management Systems, In-process Audits) Root Cause & Corrective Action (RCCA) Human Factors Continuous Process Improvement.
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Identifies automation opportunities and responsible for implementation, development and maintenance of test Automation Framework architecture, works closely with Developers, product, & stakeholders in developing automated and functional test cases using qTest, Zypher or QTP/UFT, Selenium, Postman, Python, JMeter, Java, C#, EDI/ETL, Postman, JMeter, RedGate, SSMS, Query Surge, Informatica, Load Test Tools.
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This role will include participation in cross-functional teams such as those with a focus on facility design, chemical and electrochemical engineering, I&C and software engineering, process modeling, quality assurance, and licensing.
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Process development and product development for new vape, concentrate, and infused productsConduct process troubleshooting and root cause analysis to resolve manufacturing issues, ensuring minimal impact on production schedules and product quality.
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Responsible for quality control through production sheet accuracy, recipe development and product condition/presentation. ROLE AND PURPOSE: To plan, organize, implement and coordinate menu/production record management and product quality control in the district with consideration to healthful food selections and all national, state and local regulations.
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Develops and analyzes statistical data and product specifications to determine present standards and establish proposed quality and reliability expectancy of finished product. Provides inspection activity for product throughout the production cycle.
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Summary: As the Quality Assurance Manager, you will be responsible for managing the quality assurance programs for the Green Plains Shenandoah, Iowa site, as well as managing the quality control lab of the new Clean Sugar process, while also supporting the goals and objectives of the company.
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Summary Manages the quality assurance/quality control (QA/QC) program and fermentation for the ethanol plant to ensure maximum production quantity and quality, while supporting policies, goals and objectives of the company.
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PeopleShare is seeking a HYBRID Quality Assurance Analyst for an innovative, industry leading healthcare company in Whippany, NJ! 1 to 3 years in a quality assurance or quality auditing role preferably in a call center, claim operations, pharmacy hub, or similar environments.
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Manage and lead the Mission Assurance team of quality engineers supporting the Lynnwood & Poulsbo sites. Actively oversee the implementation of Mission Assurance goals and objectives and support Quality Engineering & Control business rhythms.
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This position has a strong cross-functional partnership with the Cell Therapy Business leaders, Process Engineering, Technology Transfer/New Product Introduction to ensure successful development and transfer, into the site, of all client cell therapy manufacturing processes.
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product development production quality assurance process jobs Company: Nsf
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