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The ISO Quality Specialist will be responsible for development, implementation, and maintenance the organization's Quality Management System for non-GMP products. The primary responsibility of the Quality Specialist is to maintain the adherence to quality standards for non-GMP products.
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Sr. Quality Engineer. This involves the development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS, RTU), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client's facility.
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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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The Quality Control Analyst will work within the QC team, testing gene therapy products utilizing cell-based assays (Potency assay) in support of clinical and commercial lot release and stability activities.
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Responsible for Quality System records associated with analytical testing (change control, lab investigations, OOS, deviations, and CAPAs)Establish and maintain Sarepta’s specifications and sampling plans for in-process, drug substance, drug product, and stability.
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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 certifications like ASQ Six Sigma Green Belt or Black Belt, CQE, etc. Job Title: Quality Systems Engineering Manager. Excellent knowledge of Quality Management System (QMS) in high volume semiconductor, or electronics manufacturing environment.
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The Quality Engineer is responsible for monitoring and maintaining the overall quality of manufactured products at Teledyne FLIR’s Billerica facility. Assist the supplier quality team with supplier-lead/driven root cause investigations.
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Quality System owner of Nonconformances (NCR), Corrective and Preventive Action (CAPA), Customer Complaints, and Change Control among other systems. This is a collaborative position working closely with Operations to support production management and production initiatives while ensur ing compliance with AVIs Q uality Management System (QM S ) and FDA Quality System Regulation ( QSR ) requirements.
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Position works in Quality Control to ensure product specifications are strictly adhered to by performing incoming, first sample, in-process, and final quality control inspections of product using a microscope and various measurement tools.
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The Design Quality Engineering Co-Op will partner with new product development teams on one of the most dynamic innovations in Abiomed’s pipeline. This opportunity will allow the candidate to advance their technical knowledge in MedTech quality and compliance, design characterization, new product development and industry standards while also gaining experience with working with multidisciplinary teams to achieve impactful business results while advancing the future of innovation in Johnson and Johnson MedTech at Abiomed.
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Principal Quality Engineer- RF & Microwave. The Principal Quality Engineer will be responsible forsupport of multiple business units across various key commercial andAerospace and Defense programs.
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Certified Manager of Quality/Organizational Excellence preferred. Manage processes to address customer complaints and manufacturing & supplier quality issues. Define & proactively manage company production & supplier quality requirements.
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We are looking for a Quality Engineer/Manager professional to join our team. Quality Engineer (This is NOT a remote position) Work closely with Engineering, Operation and Test departments in establishing, implementing, and enforcing quality requirements for the manufacturing and testing of electronics assemblies, components, circuit boards and systems.
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Minimum of 7-10 years quality assurance / supplier quality engineering experience in a pharmaceutical/life-science environment. Provides Quality support and Technical direction for New Product Development, technology transfer, and process validation activities.
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Title: quality Company: Wts Energy in Andover, MA
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