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Good fit for anyone with sales experience in the water quality/water filtration industry. Conduct territory site visits offering our water quality, conditioning, and filtration solutions.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Quality Specialist will be responsible for performing scheduled audits and random spot inspections of the work in progress, the final/finished product and project quality document control to verify these items have been completed in compliance with all applicable codes, standards, plans and specifications, and meets customer requirements and expectations.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Our technologies include raw water pretreatment, filtration, ion exchange, demineralization, degasification, hot lime softening, boiler make-up, condensate polishing, wastewater treatment, cooling, and oil/water separation for markets such as petrochemical/chemical, power generation and heavy industrial plants.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Stock, restock, and organize raw materials and finished products in assigned warehouses. Inspects, receives, and samples all raw materials for manufacturing areas and scans and transfers items as needed.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Performs chemical analysis of raw materials, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques, adhering to company policies as identified in standard operating procedures (SOPs.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Reporting to the Senior Director, Quality Assurance & Regulatory Affairs, QMS Engineer will play key role in managing Quality Management System; Quality Engineering functions; Internal & External audits, Validation, and Document Control.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Define, own, and execute R&D Quality processes contributing to Drug Development's end to end Risk Based Management (RBM) framework across the clinical trial portfolio. This involves collecting all the relevant inputs from the RBM framework as well as R&D Quality Clinical Quality inputs from audit and inspection.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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This position reports to the President and CEO of Gan & Lee Pharmaceuticals USA. The Clinical Quality Director leads all GxP (GCP mostly) audits/inspections at the US Affiliate. At least 10 years in relevant quality auditor roles in which significant exposure to GCP/GLP has occurred.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Also, audit the vendors (raw materials, packing materials, contract testing laboratories, or other service providers) as per the in-house SOP to ensure that all vendors comply with cGMP standards.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Will consider candidates who commit to complete additional Guidewire curriculum for the Quality Assurance Analyst role within first 6 months:Base Curriculum Overview - Consisting of Cloud, SurePath, Implementation Tools, & Testing FrameworkCompletion of InsuranceSuite Analyst Associate ExamRecent Guidewire certifications, or related work experience in Hakuba, Jasper releases.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. Experience in assay transfer, technology transfer, validation from Analytical Developmental group to Quality Control group.
$42 an hourExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Reporting to the Production Manager, this role is responsible for the production of the product portfolio including raw ingredient/product component (materials) management and blending, manufacture, storage, inventory, logistics, facilities, site health and safety and site risk management.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Quality Engineer will work in collaboration with the development team to ensure GNY business needs are reflected in the quality and usability of the Guidewire Cloud version of Policy Center, Billing Center, and Integrations.
$145,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Reporting to the Associate Director, Quality Management Systems (QMS), the Quality Engineer CAPA and Systems, will play a key role in managing QA and Regulatory Compliance activities for Insmed.
$97,200 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The position interfaces with experts in Process Development, Manufacturing Sciences and Technology, Operations, Analytical Development, Quality and Regulatory Sciences. Document Specialist, supports the documentation activities for regulatory submission content and supporting documentation for cell therapy portfolio.
Full-timeExpandApply NowActive JobUpdated 1 month ago
raw job Title: quality in Piscataway, NJ
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