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Integrate enterprise applications, develop automated workflows using Dell Boomi or similar tools and ensure data quality and consistency across different systems. Proficient in automating workflows and enterprise Integrations using Dell Boomi or similar middleware tools.
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Our areas of expertise include remote sensing, geospatial analysis, GIS, soil science, water quality and demand evaluation, agricultural systems, salinity and nutrient management, ecosystem restoration, statistics, and regulatory policy.
RemoteExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Prepare reports by collecting, analyzing and summarizing data through Microsoft Dynamics 365 (Business Central) and Power BI. - 5-8 years of experience in a manufacturing quality manager, quality supervisor, or senior quality engineering role.
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The ideal candidate will be excited about the opportunity to maintain and grow our environmental consulting business and possess knowledge and technical skills in storm water management, TMDLs, bacteria indicators, water quality resources, water quality modeling, environmental permitting, and municipal, commercial and industrial NPDES compliance.
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Assist with preparing environmental survey reports, data entry, impact assessment, and assist with permitting activities for assigned projects (e.g. Endangered Species Act, Clean Water Act permitting, CEQA, NEPA, etc.
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Supervise QC analyst(s) Responsible for QC data/records to ensure content adheres to established cGMP quality standards. Manage the analytical testing of products (in-process, for information, and release) Review the testing schedule with the QC Supervisor Perform day to day analytical testing activities in GMP QC lab to support the on-time release and periodic testing of biological drug products using complex instrumentation and laboratory equipment’s per regulatory/quality policies.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Proactively provide Good Pharmacovigilance Practice (GVP) support for clinical and commercial activities to protect patient safety and well-being, maintain data integrity, and support implementation of Quality Systems.
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O Support the PrEP Monitoring and Evaluation team in monitoring and evaluation of quality of PrEP programs, including participating in regular data review and analytics with the Surveillance Unit.
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A Certified Registered Nurse Anesthetist (CRNA) in an advanced practice registered nurse (APRN) who practices both autonomously and in collaboration with a variety of health providers on the interprofessional team to deliver high-quality, holistic, evidence-based anesthesia and pain care services.
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The selected candidate will be responsible for all aspects of Quality Control oversight, including external (CDMO) release and in-process assays, raw data review, method qualification and validation, stability, trending and GMP investigations for any analytical deviation, OOT or OOS. The ideal candidate must have experience with cell therapy analytical techniques, including flow cytometry, PCR (qPCR, QF-PCR, ddPCR, and/or dPCR), ELISA, safety-based assays (sterility, mycoplasma, endotoxin, etc.
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Review of analytical release and stability data, involving review of Potency tests of investigational new tablets and capsules using High Performance Liquid Chromatography (HPLC) or Ultra Performance Liquid Chromatography, Water Content using Karl Fischer Titration and Karl Fischer Oven, physical characterization of crystalline and partially crystalline solids using tests like Powder X-Ray Diffraction (PXRD), Thermogravimetric analyzer (TGA) and Differential Scanning Calorimeter (DSC.
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Data Quality Analyst - Healthcare data management. Healthcare data management, data quality, sQL, Mongo, ETL Data Warehouse, SAS, SDLC, project management, master data management tools, data quality.
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The QA Associate must be familiar with applicable GMP. This individual will be responsible for evaluating the compliance of manufacturing and analytical documents such as test methods, batch records, stability and release data, etc.
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The Clinical Laboratory Scientist will perform assays in accordance with the Company’s CLIA quality management systems and will work closely with and be part of a dynamic, multi-disciplinary team responsible for quality assurance, client services, data management and clinical research.
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Pharmaceutical industrial engineering knowledge (pharmaceutical design, development, manufacturing, and regulatory requirements) to optimize technical transfer from lab-scale to kilo lab/pilot plant production; Implement hazard operability analysis and risk assessment skills to draft batch records and safety reports; Analyze lab and production data using NMR instrumentation, data interpretation, Chromatography to ensure FDA regulatory compliance and maintain quality standards.
$93,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago
data quality jobs in San Diego, CA
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