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Strong prior experience in Quality Assurance initiatives including post market surveillance, complaints management, quality KPls, Design Controls, Risk management, CAPA, Quality Management Review, Audits, and Supplier Quality.
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Formal training in continuous improvement methodologies required (e.g., Lean Manufacturing, TPS, Six Sigma, Total Quality Management, Theory of Constraints) This position is a key member of a regional leadership team, driving an end-to-end analysis of the regional Business Operations & performance measures, identifying cross-functional system view of opportunities for profitable growth, and driving business transformation leveraging the Quest Management System (QMS) specifically focused on Continuous Improvement (CI), system thinking, and big data analytics techniques (adopting AI.
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Collaborate with Advanced Manufacturing Engineering on fixture development, process improvements, corrective actions, and any other measures needed to drive continuous improvement within the group.
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One of your tasks will be to drive continuous improvement initiatives within the QMS, including CAPA, change control, and risk management processes. As the Quality Assurance Lead, you must possess a strong background in Quality Systems, Document Control, Supplier Quality, and Validation within the biotech industry.
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SWCM provides innovative solutions through automation, continuous improvement, and a skilled workforce providing support for all digital computing products: embedded software, firmware/configurable logic, test equipment, simulation, Commercial-Off-The-Shelf (COTS) and tools.
$77,000 - $163,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Responsible for any new buildings from frame up to completion quality assurance weekly visits. Ensure workmanship/quality throughout project process with completion sign off. 5+ years in construction trades or facility management position.
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Experience of working under own initiative and in planning and prioritizing workloads University or technical college degree or equivalent qualification in relevant sciences such as: Medicine, Pharmacy, Chemistry, Biochemistry, Biology, Microbiology, Biotechnology, Health Technology, Toxicology, Physics, Biophysics, Material Science Biomedical Engineering, Mechanical, Electrical or Electronic Engineering, Computer & Software Technology, Human Physiology, Nursing, Quality Management.
$103,500 - $170,800 a yearFull-timeRemoteExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Provides project management support for DFW habitat conservation and improvement programs. MINIMUM ENTRANCE REQUIREMENTS: Applicants must have at least (A) three years of full time, or equivalent part-time, professional, administrative or managerial experience in business administration, business management or public administration the major duties of which involved program management, program administration, program coordination, program planning and/or program analysis, or (B) any equivalent combination of the required experience and the substitutions below.
$67,349.36 - $97,344.26 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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To join a team of 120+ Software Engineers that are developing and supporting our several Air Traffic Control Systems worldwide, such as: Our programs are safety-of-life air traffic management systems we have developed for the FAA and international equivalents for use by air traffic controllers controlling civil and military aviation.
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Demonstrated experience in implementation and continuous improvement of the QMS and risk management tools to improve quality, reduce costs and improve efficiency. In-depth understanding of quality assurance and engineering and related tools, FDA QSR, EU MDR, MDSAP and ISO standards relating to regulation of Medical Devices.
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Applicants must be formally registered in a graduate degree program, earned 18 or more credits (by their APP internship start date), towards the completion of a graduate degree, including but not limited to public health, public policy, health professions including nursing, medicine, and allied health, human services, economics or finance, health management or administration, law, statistics, informatics, or social and behavioral health.
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Applicants may be formally registered in an academic program working towards the completion of a Terminal Degree in certain fields, including but not limited to public health, public policy, health professions including nursing, medicine, and allied health, human services, economics or finance, health management or administration, law, statistics, informatics, or social and behavioral health.
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Under the direction of the Project Director/Lead and functionally reporting to the Advanced Manufacturing Engineering Director, the Document Controller will establish, plan, control, and direct the full scope of document/records management program activities for the project.
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Must be capable of completing assembly and test records for regulatory and quality control requirements. Ability to cooperate with others in a team effort to achieve quality, safety and productivity goals.
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Ensure the accomplishment of site objectives to meet patient demand for on-time delivery of medicines according to Quality, GMP, Safety, Environmental, and performance standards as well as statutory, regulatory and other company requirements with continuous improvement mindset.
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continuous improvement program quality assurance engineering management jobs in Marlborough, MA
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