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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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SUMMARY The purpose of the position is to provide a Quality Assurance (QA) Engineering Technologist to support projects within SAO that have the complex, contractually mandated quality assurance requirements associated with NASA space-flight hardware fabrication and to provide guidance to CFA scientific investigators in defining, proposing, and conducting instrumentation projects with quality assurance requirements.
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Partner with Manufacturing, Engineering, and IT to ensure that computerized quality systems are compliant with Abiomed procedures, FDA Quality System Regulations, 21 CFR Part 11.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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We are seeking a self-motivated and fast learning Systems Engineering Intern with passion and background in at least two or more of the following areas: signal processing, embedded firmware development, software development, PCB design, analog/digital circuits design, and FPGA prototyping.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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This individual will work closely with CMOs, CMC, Regulatory, Clinical, Quality Systems, Validation and Supply Chain Operations teams to maintain drug product supply. This includes collaborative interactions such as due diligence, establishing and maintaining quality agreements, review of change controls, deviations, CAPA and metrics as well as providing support to build effective quality systems and supporting continuous improvement activities.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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5+ years proven experience working with large cross-functional engineering teams with modelling, simulation, testing, integration and/or quality assurance domain expertise. This person will partner with (1) the Product Teams to drive high quality product delivery, (2) the QA Manual Testing and Requirements Team to synchronize virtual and physical tests, and (3) the internal Customers (Operations, Maintenance, Process, Ops Engineering, etc.
$121,000 - $235,200 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Years’ experience: 5 or more years of relevant test and quality assurance experience with 3 years’ experience in system and subsystem testing. The Engineering team will research, design, and integrate sensors, platforms, computer systems, and network solutions as guided by the systems requirements documents.
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Maintain robust GMP quality systems, including documentation, change control, deviations, CAPA, and quality events. A minimum of 7 years of experience in GMP quality assurance within the biotech or pharmaceutical industry, with direct experience in auditing and the manufacture of monoclonal antibodies or biologics.
$170,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Support Associate Director in the management of PECO’s Quality Assurance program in partnership with key stakeholders to support multiple customer-facing teams of varying tenure and experience.
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A successful candidate will have deep quality engineering experience with high-volume manufacturing of complex electro-mechanical systems, printed circuit boards, and printed circuit board assemblies.
$140,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Lead Responsibilities: Lead in the provision of engineering evaluation & determinations, issue technical direction & guidance, and oversee Inspection & Quality Assurance initiatives for all mechanical equipment and pressure systems troubleshooting, maintenance, calibration, repair, and test activities.
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The Software Quality Assurance Testing Engineer will play a key role in the quality assurance of Anti-Money Laundering (“AML”), Sanctions Screening, AML Transaction Monitoring, and Know Your Customer (“KYC”) suite of applications in the Boston, MA area.
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Responsible for the appropriate utilization and staff compliance of the Quality Assurance (QA) program on assigned unit to encompass all aspects of treatment, treatment delivery and quality patient care.
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Or, alternatively, Master’s degree (or foreign education equivalent) in Computer Science, Engineering, Information Technology, Information Systems, InformationManagement, Business Administration, or a closely related field and four (4) years of experience as a Director, Software Engineer (or closely related occupation) leading a team ofengineers in the design and implementation of Content Management Systems (CMS.
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
Full-timeExpandApply NowActive JobUpdated 9 days ago
systems engineering quality assurance jobs Title: program in Wakefield, MA
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