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Main Duties and Responsibilities:Develop and direct the implementation of changes to Process Control, Quality Control and Quality Assurance procedures to improve product quality, reliability, yield and cost effectiveness.
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Adaptable to perform in a fast-paced environment while still delivering high-quality results, this Analyst I - QC Molecular Biology will be required to have strong interpersonal skills and be able to work under minimal supervision.
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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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Preferably knowledge to handle SAP, EDMS, LMS, Master Control etc. who will be providing scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product quality complaints; ensures compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) and Quality Management System standards, compiles monthly Quality metrics for internal and corporate review, and analyzes trends to implement corrective and preventive actions to mitigate adverse trends.
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A day as a Quality Control Technician I (Monday - Thursday, 05:00 am to 03:30 pm) in Cirtec Medical. Assist with qualification and validation processes under Quality Engineer (QE) oversight.
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Team-oriented, customer-focused work ethic and time management skills Experience with Microsoft Office, MS Word, and MS Excel Well-developed problem solving and decision-making abilities Attitude of collaboration and desire to develop through learning Experience with metals a plus, but not required—we will train Job Description The Quality Control Inspector conducts first piece, in-process, and final inspections of parts and products throughout the entire product flow in production.
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Knowledge to handle SAP, EDMS, LMS, Master Control etc. and continuous improvements and compliance of Quality Management Systems (QMS) following FDA and ISO regulations. oversight of the vendor/supplier management Program and work closely on device issues and develop quality vendor/supplier agreements with all key vendor/supplier.
$160,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Associate Quality Control Principal role, within our not-for-profit and governmental group is responsible for managing technical accounting and auditing matters in the Firm, including research and overseeing quality in the Firm's accounting and auditing practice to help ensure compliance with professional standards.
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Communicates and educates Value Stream Team on matters requiring specialized knowledge of quality functions, i.e., Production Approval Process (PPAP), Advanced Product Quality Process (APQP), and document control.
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The Quality Engineer (electronics / defense) will be responsible for ensuring supplier compliance in delivering complex military products by overseeing the control and inspection of incoming materials.
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Position Summary For Material Handler 1 (Picking/Selecting & Checking/Quality Control) : Material Handler 1 is responsible for picking, selecting, checking and ensuring the accurate transportation of materials, stock, merchandise, supplies, and other finished products to designated locations including preparation for shipment.
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Job Description Roles and Responsibilities: Job Title: Quality Inspector, level 3. Ongoing Training (RSO, Systems, Software Programs, OSHA Safety, JJ Keller, etc.) Will enter inspection results into QMS and MRP systems, and work with engineering to report and detail non-conformances.
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Lead the development and implementation of enhancements to Process Control, Quality Control, and Quality Assurance procedures to improve product quality, reliability, yield, and cost-effectiveness.
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Support quality control testing and run the quality control department. Job Title: Quality Control Manager. Experience with adhesives and chemical testing is required.
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Common SWQE tasks involve review of SW Release Packages (Windchill PDM, Azure DevOps Server), CDRL Deliverables (IR, CN, ECP), SW Investigation Requests (SIRs), SW Trouble Reports (STRs, Code Reviews), Physical Media (Loader Verifier), Test Artifacts, and participation in Peer Reviews (SW, SE), Control Boards (SRB, SSRB), Tracking Books (Metrics Monitoring), Command Media (Policies), Test Witnessing (SQT, FQT), Audits.
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quality control jobs Title: quality in Wilmington, MA
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