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At least 12 years in the areas of Test, Wafer fab, Assembly, Failure Analysis, Product Engineering, Reliability, Supply Chain or Quality. Nearest Major Market:WoburnNearest Secondary Market:Boston Job Segment: Supply Chain, Quality Engineer, Manufacturing Engineer, PLM, Network, Operations, Engineering, Management, Technology.
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Collaborate with cross-functional teams to establish and maintain quality assurance processes throughout the manufacturing lifecycle (NPI through end of life) Abiomed, a part of Johnson& Johnson MedTech, is currently recruiting for a Manager, Quality Engineering.
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This individual will support quality control activities related to custom raw material manufacture for RNA and AAV gene therapy products conducted both internally and at various contract manufacturing organization (CMO) sites.
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The Quality Control Laboratory Support Technician (RP/ISO) is responsible for inventory management, glassware cleaning, and basic equipment verifications within the Quality Control department.
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Experience being responsible for quality control of all scientific data generated within the Nonclinical Pharmacology group. This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group within GNAT unit of client.
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Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I, that will be primarily focused on wet chemistry, based onsite in our Andover, MA facility. The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw materials, in-process and finished formulations under general supervision and in accordance with standard operating procedures (SOPs.
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8+ years of experience in clinical research drug development and/or Clinical Quality Assurance; 6 years with a Masters degree may also be considered. Experience with clinical quality assurance, clinical trial management/monitoring or GCP Audits.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Quality Inspection monitors the quality of incoming and outgoing products and materials for the company. The incidence and costs of quality non-conformances are constantly monitored and improved, while maintaining the highest practicable standards of manufacturing productivity and efficiency.
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Support the performance of the other appropriate Quality Assurance functions including document writing/revisions, deviations, CAPA's, document/data review and other administrative duties as needed.
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E Ink is seeking a Supplier Quality Manager who enjoys working in a fast-paced global environment, supporting manufacture of E ink's innovative materials. The Supplier Quality Manager will lead all supplier assessments, performance management, and improvement programs.
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Monitoring assurance metrics and process results. Previous work experience as a QA Engineer, QA Tester, or relevant position in the IT department with at least 3 years of experience as QA Automation Engineer.
$70,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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This position will support and participate in initiatives to drive best–in-class supplier/sourcing quality improvement. Drive continued efficiency improvements through the effective use of metrics, 5S, and the PPI process Recommend and implement changes in manufacturing procedures to improve product quality and production efficiency.
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Quality Assurance function is responsible for ensuring the effectiveness and fulfillment of the client Quality Policy, which is to comply fully in the conduct of the Company's business with all applicable regulatory and customer required specifications, and to maintain an effective Quality Management System, working in partnership with the Operations and Engineering teams to ensure that products and processes confirm to applicable standards and specifications.
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Cambridge Isotope Laboratories (CIL) has an outstanding opportunity for a Quality Assurance Specialist I to join the team responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components based onsite in our Tewksbury, MA location.
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Job Overview: This role, for a Document QC Specialist Contractor, will manage the quality control of scientific documents and Bioanalytical data for the Translational DMPK and Clinical Pharmacology group.
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quality job Title: supplier quality assurance in Billerica, MA
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