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Reporting to the Production Supervisor , the Quality Supervisor Supervises and coordinates activities related to the Quality Assurance Inspection function, on the manufacturing floor. Quarantine and disposition of nonconforming goods, while ensuring the policies and processes are followed.
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Direct and participate in the training and development of employees in the facility’s procedures and methods for operating all non-destructive testing equipment Direct and participate in the preparation of samples or specimens for non-destructive testing of materials and components during the various stages of manufacturing and assembly Monitor and audit all NDT related processes Review rejected material or components for defect severity and disposition.
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Engage customers to gather job requirements and translate customer requirements in to detailed manufacturing/kitting instructions and shipping/postal instructions for disposition of the customers & products.
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The Specialist, Manufacturing Technical Investigations and Analytics (MTIA) will work collaboratively across departments to ensure a state of compliance exists within Vertex Manufacturing Center (VMC), manufacturing, facilities and warehouse operations.
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Knowledge of manufacturing processes such as additive manufacturing, casting, milling, turning, grinding, drilling, etc. Design cost effective easily manufacturable hardware taking into account: tolerance stack-ups ease of assembly meet customer installation requirements materials of construction methods of manufacture mechanical environment (Thermal and Vibe) and Application Loading preliminary analytical results (Hand calcs and FEA) mistake proofing Disposition non-conforming hardware and correct production/vendor issues.
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Collaborate with Materials Manager, Process Engineer, Purchasing and KAM to effectively manage program material purchase, inventory, and disposition at the company. About the Company Our client is a premier, global Contract Manufacturing and Development Organization (CDMO) and partner the pharma industry trusts most to deliver innovative oral, transdermal, and intradermal drug delivery systems.
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Must possess an associate degree in Electrical, Mechanical, or Electro-Mechanical/ MechatronicsEngineering, or related degree and/or a minimum of 3 years experience or training preferably in a similar type of manufacturing environment.
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The Contract Manufacturing Manager will interact with and support Marketing & Sales as well as all other functional departments including Operations, Logistics, Demand Planning, Quality, Research & Development, Procurement, and Finance across within the Post Consumer Brands business unit and across Post Holdings.
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Determine root cause and corrective action of non-conforming product and disposition MRR in Baan. Fully enclosed shoes of solid, leather construction with a steel or composite toe cap (ANSI Z41 compliant) must be worn in all manufacturing areas, including the Shipping / Receiving areas.
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Batch record review and product disposition. The Quality Assurance Manager will ensure compliance with current Good Manufacturing Practices (cGMP) as they pertain to the local regulation and exporting countries regulation as applicable (such as FDA, MHRA, EMA, Health Canada.
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Contribute to process improvement of batch records and turnaround times to ensure turnaround times and QA batch disposition deadlines. A Minimum of 0-2+ years Biotech/Pharmaceutical experience or equivalent industry experience Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products as well as knowledge of Good Tissue Practices.
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Coordinate the introduction of production from design, to supplier, or in-house fabrication, into the manufacturing environment, oversee assembly of machined and fabricated components, and integration/inspection of assemblies, and disposition of non-conformances.
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Knowledge on Good Laboratory Practices (GLP) - Standard Operating Procedures (SOP) - Good Manufacturing Practice (GMP) Primary liaison for any sorting activity and the proper disposition of that material.
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As a Manufacturing Probe Process Engineer in the Test Solutions Engineer (TSE) Key Equipment Group (KEG), you will have responsibilities for supporting and maintaining Probe processes and software that are co-developed with Micron's Global Manufacturing sites, or directly sent to the Manufacturing sites around the world.
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Reporting to our Senior Manager, Quality Assurance CMC, this position is responsible for managing, reviewing, and approving quality documents from Contract Manufacturing Organizations and Contract Testing Laboratories for manufacturing, testing, validation, and disposition of clinical and commercial products for human use.
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