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With $180M raised and backed by venture partners like Capricorn, NVIDIA Ventures, True Ventures, General Motors Ventures, Denso, Porsche SE, SIP global partners, Honda, Xerox, Cubit Capital, Siemens Energy, and Maniv Mobility, our Area Printing process manufactures components at price points and quality levels that compete directly with conventional manufacturing techniques of machining and casting, delivering high-volume, localized and decarbonized manufacturing.
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Support Manufacturing, Quality Control and Assay Development by shadowing the process and providing beneficial feedback and knowledge on the process. Support continuous improvement efforts, by evaluating potential process changes in manufacturing and quality control.
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Requirements: Master's degree in Regulatory Affairs, Engineering, Life Sciences, or closely related technical discipline (willing to accept foreign education equivalent) and five (5) years of experience as a Regulatory Affairs Specialist or experience executing the complete lifecycle of product registrations before national and international regulatory agencies, including documenting internal processes for quality control, and coordinating post-market surveillance and reporting activities.
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Statistical Process Control (SPC) Statistical Process Control. This role manages technical quality assurance, oversees manufacturing QA/QC practices, conducts inspections, and coordinates supplier audits, requiring expertise in GD&T, SPC, and strong communication.
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Have a willingness to learn new things, possess skills in metrology and receiving inspection, prior experience in laboratory or technical field using chemicals proves useful, prior experience with statistical process control, measurement gauges of all types, good customer and communication skills at all levels, good positive attitude and work ethic.
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This role will provide overarching QA support including directing implementation of QA/QC practices into the manufacturing process, drive standard work, monitor staff performance; including aligning staff to appropriate areas based on skills/capabilities.
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Manage the corrective and preventive action (CAPA), management review process, and internal quality audit programs Manage Non-Conforming Material Reviews and MRB activities Manage supply chain quality, supplier audits, supplier approvals and supplier corrective actions Manage documentation control and record-keeping systems for engineering documents and company procedures; Includes Environmental control procedures.
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A day as a Quality Control Technician I (Monday - Thursday, 05:00 am to 03:30 pm) in Cirtec Medical. Compile and analyze statistical data to assess process capabilities and control processes.
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Experience with DeltaV Process Control System and SAP in a cGMP environment is desirable. Actively leads a bulk chemical manufacturing production line working with other shift supervisors to ensure consistency across all shiftsDevelops weekly production schedule by partnering with Production Planning, Supply Chain, Quality, and Product Management teams.
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Duties: Provides overall leadership and management of all aspects of company and supplier quality for continuous process improvement and high-quality output. Experience in Total Quality Management and process improvement.
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You will own and process Quality Management Standard documents - including ISO forms, Return Material Authorizations (RMA) and quality control action plans. You will receive, process and place client orders including scheduling shipment of goods via land, air and or sea.
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May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
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The position requires knowledge of quality systems, statistical tools, lean six sigma methodologies, process capability, and understanding of control plans and process flow.
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Working knowledge of FDA/QSR, ISO/EU MDR standards, process validation, product design control, CAPA, and FMEA methodologies. Responsible for coordinating initial component quality requirements, including first article inspection, process qualification, and assisting in supplier validation activities such as writing/approving protocols.
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To ensure the QMS implementation will meet their needs, (2) the Quality Assurance (QA) Execution team to ensure alignment and consistency of the manual, virtual and process validation with the QMS specifications and (3) the QMS Design Manager to ensure the QMS implementation will adhere with specifications and will include all the relevant procedures and instructions.
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quality control process jobs in Tewksbury, MA
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