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Seurat’s proprietary Area Printing process, developed at Lawrence Livermore National Labs (LLNL), allows metal components to be manufactured at price points and quality levels that compete directly with conventional manufacturing techniques, enabling the reshoring of supply chains and promoting the decarbonization of industry.
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Support the configuration control function to include receipt, dissemination, processing, tracking, and providing recommendation for the final disposition of Advanced Change Study Notices, ECPs, Requests for Deviation/Request for Waiver, Deficiency Reports (DRs), Airworthiness Directive Notes, Service Actions, Service Bulletins, Aircraft Service Changes, Notices of Deficiency, and Quality Control Plans (QCPs.
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Initiate, investigate & close quality systems (deviation, NCMR, CAPA, change control) The successful candidate will be responsible for performing the necessary tasks to complete Design Control projects, contributing to the development of high-quality LDT and IVD products.
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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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SENIOR ASSOCIATE COMPLIANCE - (Product Quality) 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.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of vendor/supplier management Program Working knowledge of Trackwise to handle electronic Quality Manage System (eQMS) data, EDMS for SOPs and LMS for trainings. Ensure compliance of establish Quality Management System (QMS) and in compliance with corporate requirements and all applicable FDA Part , Part /, Part , ISO and Canadian Medical Devices Regulations (CMDR SOR/-), EU Medical Device Regulation.
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All Internal Manufacturing, Materials Management, Technical Operations and Facilities Management with limited exposure to support groups (Validation, Quality Control, Process Development and Health, Safety & Environment.
$35.43 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Previous experience in Quality Control, Manufacturing and/or Engineering preferred. Quality Assurance and Control. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies.
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Review, evaluate and monitor acquisition Contractor drawings for completeness, currency, technical accuracy and conformance to requirements, specifications, regulations and quality control to ensure compliance with ASME technical Data Package format and requirements.
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TMT Academy Set strategy and drive evolution of our core internal learning programme Oversee and quality control delivery of content, communications and event calendar Utilize internal analysis to innovate and evolve program based on results and priorities.
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Skills: Quality control, MS-EXCEL, ICH Regulations, GMP (Good Manufacturing Practice), Manufacturing Operations. We are seeking a Senior Quality Analyst to maintain supplier performance metrics, develop trend data of supplier related processes, log and track supplier quality events utilizing the company's Quality System, and conduct audits of external suppliers for Positron Emission Tomography (PET) products.
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The Watts Water Technologies family of companies designs and manufactures valves and drains and related products that promote the comfort and safety of people and the quality, conservation and control of water used in commercial, residential, industrial, and municipal applications.
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We are seeking a highly skilled Senior Software Engineer to design and implement functional emulation solutions for simulating Robotics Control Systems. Developing high-quality software design and architecture for our emulation product.
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We have an immediate need for an onsite Senior Software Systems Quality Engineer (Quality Assurance/Compliance) to support Land & Air Defense Systems (LADS). 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.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Typically requires a Bachelor's degree in Science, Technology, Engineering or Mathematics (STEM) Education and five (5) years of Quality Experience (Assurance, or Compliance, or Engineering) or Engineering Experience.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago
quality control jobs Title: senior in Billerica, MA
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