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Supports Trackwise Digital Quality R&D Division process improvement projects (UAM/UAT testing). Reviews quality events, deviations, investigations, and change controls. Experience in quality oversight of R&D/Clinical product manufacturing and packaging Experience in TrackWise Digital If you meet the required qualifications and are interested in this role, please apply today.
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Quality Engineering Engineers generally will be placed into one of the following types of roles: Process Engineer, Project Engineer, Manufacturing Engineer, Reliability Engineer, Process Control Engineer, or Quality Engineer.
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We are looking for a dedicated Construction Quality Control and Quality Assurance to join our talented team at our office located in Somerset, NJ.In this role, you will use your technical knowledge and skills to effectively train, supervise, communicate, execute, and manage the IPS Construction Quality Control and Quality Assurance (QA/QC) program for ongoing Construction Projects.
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The QC Chemist will play a critical role in maintaining the integrity and quality of products. PeopleShare is currently hiring for a Quality Control Specialist in Plainsboro, NJ! The Pharmaceutical QC Specialist is responsible for conducting various analytical tests and ensuring the quality and compliance of pharmaceutical products with regulatory standards.
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Cross-functional collaboration/interaction with Clinical Affairs, R&D, Regulatory, Quality, OEC, Legal, Global Marketing & Commercial teams. Our i-STAT System is an advanced, portable diagnostic tool that provides real-time, lab-quality results within minutes to accelerate patient-care decision-making.
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Knowledge of key concepts including unit operations, processes, quality by design (QbD), tech transfer, process validation, quality attributes, and regulatory milestones across pharma development.
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This role will establish a centralized capability, aligned with Otsuka IT, to design, create, test, deploy, manage and maintain the D&A architecture, as well as work with partners within D&A to enable data collection, curation, quality, consolidation, preparation, testing, deployment and maintenance of databases.
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Position Summary / ObjectiveThe Senior Manager, GRS-CMC is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions regarding: Clinical trial applications; New marketing applications; HA responses & background packages (including participating / leading HA meetings); &/or post-approval submissions.
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The goal of the position is to help program participants improve their food security; dietary quality; physical activity; and food safety behaviors. Office may be located at Rutgers Cooperative Extension of Burlington, Camden, Gloucester, Mercer counties.
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The Assoc II, Warehouse Ops assists on Inbound or Outbound activities as requested by the Warehouse Supervisor meeting quality, safety, productivity and operational standards. Follow established Standard Operating Procedures (SOP’s) to process orders including accurately picking, performing quality control checks, sorting, consolidating freight, building, and wrapping pallets, packing, loading, and preparing orders for shipment.
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The Behavioral Health Quality Management Supervisor shall report to the ABHNJ Quality Management Director and will work in close partnership with the ABHNJ Behavioral Health Medical Director, Behavioral Health Administrator, CMO, Behavioral Health Director of Network Relations and all matrixed growth partners to effectively manage access and quality of behavioral health benefits and care.
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Educate all new Customer Service personnel on the Quality Assurance Program globally. At least one year of experience performing a Quality Analyst role in a similar environment or equivalent quality assurance activities in a customer-facing role.
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Monitor the quality of toxicokinetic reports that are generated by other TK scientists by checking the raw data outputs and ensuring quality of reported data in the reports, in addition, serve as a TK quality control inspector to ensure the efficiency and effectiveness of TK data/report generation process.
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Take samples from raw materials and finished product for testing, while adhering to Quality Control requirements. You’ll be supported by your team with possibilities to grow into a Manufacturing Professional and directly impact the quality of our products – helping to improve real lives.
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Identify, evaluate, and implement new technologies and methods to improve upon the quality and efficiency of high-throughput receptor in vitro pharmacology HTS campaigns and SAR profiling. Chemistry is a core capability in Small Molecule & Drug Discovery with innovative scientists working in medicinal chemistry, radiochemistry, analytical chemistry, and large-scale synthesis.
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