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Support Alpla North America Integrated Management and Quality Assurance systems through projects and initiatives in the regional Quality Department. Responsible for providing quality related support to all plants in Alpla North America.
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A minimum of 2 years of experience in quality engineering or related field with application and implementation of (GMP/QSR/ISO/MDD and Canadian Medical Device) regulations a plus, with focus on, process validations, product development supports.
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A quality tech is responsible for examining materials for flaws and deviations from the original product specifications. We are currently searching for dedicated Quality Tech to join our team.
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Description: Client, provider of some of the world's most advanced, technology-led defense, aerospace and security solutions, is actively seeking to recruit the right individual to help with our quality efforts as a Quality Assurance Laser Tracker / CMM Inspector in our Louisville, KY facility.
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Palantir Technologies is seeking a Quality Compliance Specialist to support our rapidly growing life sciences business. You will maintain day to day aspects of the quality management system (QMS), such as Document Management, Training, and Corrective and preventive action (CAPA.
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Experience developing quality control plans, supplier quality audits, failure analysis, and root cause corrective actions. 2 or more years of related experience in Manufacturing and/or Quality Engineering.
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The Supplier Quality Engineer is responsible for ensuring that delivered products and/or services conform to contractual and the Company's requirements by designing, implementing, evaluating and continually improving quality assurance and control methods and systems.
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Support tech transfer of new methods from analytical development and contract laboratories to the Quality Control Laboratory. Serve as an ADMA expert for Quality Control Chemistry, Bioanalytical, Raw Material, Microbiology, Stability, and Lab Support departments to support testing and ensure the highest level of product quality.
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A minimum of 10 years in similar cGMP environments with broad knowledge of Quality Control procedures, bioanalytical, chemistry, microbiology assays for sterility, endotoxin, TOC, and stability programs required for biologic therapies.
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Familiarity with state and federal air quality and climate change environmental policy and regulation, including NEPA, and CAA. Assignments may include development of appropriate assumptions for analysis, spreadsheet- and model-based emissions estimating, dispersion modeling, health risk assessments, and ambient air quality analysis impact analysis for NEPA documentation and as stand-alone technical reports.
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You will work closely with other functional departments within Palantir to enhance systems supporting electronic document management system (eDMS), learning management system (LMS) and CAPA. Palantir is committed to promoting a culture of diversity, equity, and inclusion and is proud to be an Equal Employment Opportunity and Affirmative Action employer.
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This position will interact with quality employees, quality manager, paving crews, asphalt plant employees, vendors, management staff, and inspectors. Resolving sample compliance with ODOT specifications and company's quality control program.
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Work within an embedded Agile/Scrum team, collaborating with your team and stakeholders to ensure quality in any products in all aspects of the software development life cycle. You must be passionate about creating quality software for our customers.
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Crane Aerospace and Electronics is seeking to hire a Supplier Quality Engineer in Burbank, CA.Job Summary:The Supplier Quality Engineer I works under supervision and uses established procedures to support the Crane Supplier Quality Management Strategy.
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3+ years of experience in the pharmaceutical industry within a GMP Quality Control role; experience with cell therapy products is a plus. Minimum of 2 years experience in the pharmaceutical industry working in a GMP quality control laboratory.
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quality job Title: field tech Company: Dhl
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