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Headquartered in Folsom, California (US) and 6 Global Delivery Centers, AgreeYa s flexible Global but Local approach delivers world class technology and business solutions around Portal and Enterprise Social Collaboration (SharePoint and SocialXtend), Cloud & Infrastructure (VDIXtend), Mobility (Onvelop), Application Development & Management, Product Engineering, Independent Software Testing, IT Staffing (Workforce Solutions) and Risk and Compliance Staffing Solutions.
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In this role, a typical day might include:The Regulatory Intelligence Manager performs proactive global monitoring and surveillance of changes in the regulatory landscape focused on the drug development lifecycle, i.e., preclinical through commercialization, as well as disseminate relevant regulatory intelligence information to Regeneron stakeholders.
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. Provide drug safety and pharmacovigilance leadership to the quality and compliance team, fostering a culture of collaboration, excellence, and continuous learning.
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Monitor assay development, assay validation and sample analysis processes, ensure timely delivery of quality results in compliance with regulatory guidance. Act as the project manager to support the externalization and operationalization of clinical biomarkers and bioanalytical activities for pre-clinical and clinical drug development.
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The Area Chief of Staff partners with the Practice Manager (if applicable) to drive the culture and delivery of quality care by the veterinary provider team (DVM, CVT, VA) in their assigned hospitals to ensure that every pet receives consistent care aligning with our six domains of quality(safe, effective, patient/client centered, timely, efficient and equitable care.
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This individual will be responsible for overseeing the planning, execution, and delivery of tech transfer project objectives in alignment with the company's strategy, commitments, and goals. Familiarity/experience with end-to-end CMC drug development.
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Supports efforts on enhancing patient experience by increasing awareness of healthcare services offered through Walgreens (e.g., patient consultation, medication management, drug therapy reviews, and perform clinical, or wellness services such as immunizations, diagnostic testing, and patient outcomes services) thereby promoting the shift of the Walgreens pharmacy role from transactional to interpersonal.
$74.8 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Qualifications Fluent in both English and Spanish required High school diploma or equivalent Must be willing to study and test for x-ray/radiology license upon eligibility. We will reimburse the cost of the test/certification X-Ray course and license must be completed within the first 6 months of employment Employee is responsible for finding a program that works best for them and their schedule CPR/BLS required prior to start date.
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Albertsons Companies is a leading food and drug retailer in the United States. The Company operates stores across 34 states and the District of Columbia with 24 banners including Albertsons, Safeway, Vons, Jewel-Osco, Shaw's, Acme, Tom Thumb, Randalls, United Supermarkets, Pavilions, Star Market, Haggen, Carrs, Kings Food Markets and Balducci's Food Lovers Market.
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Directs and provides, in collaboration with the patient, home care partner, direct and ancillary patient care staff, all aspects of the provision of safe and effective delivery of dialysis therapy to assigned patients.
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The Senior Manager is responsible for leading and supporting the Patient Experience and Delivery work within the Advance Therapies Supply Chain (ATSC), including Vein to Vein (V2V), Global Cell Collection (GCC), and Global Planning organization.
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Locally great and nationally strong, Albertsons Companies (NYSE: ACI) is one of the largest food and drug retailers in the United States. The organization includes 2,273 retail and drug stores with 1720 pharmacies, 402 associated fuel centers, 22 distribution facilities, and 19 manufacturing plants with over 300,000 employees across 34 states and the District of Columbia.
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Function as technical liaison, interfacing with internal customers, explaining Process Safety Lab capabilities and testing requirements, and authoring and publishing test result reports. Maintain detailed records of experiments, interpret test data and write test reports.
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The candidate will be building pipelines for integrating security tools in CI/CD (Azure and Github Action), publishing artifacts and performing manual code review verifying false positives from automated scanning, and writing requirements/test cases to perform a proof of concept to pick a new set of tools (for SAST, IAST, IAC, API, Secret, Container etc.
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A Conduct routine and non-routine analyses of test articles as assigned by supervisor by appropriate biochemical methods such as: SDS-PAGE, HPLC,CE- SDS, ELISA, Cell Based Bioassay, etc. Compile data and prepare graphs for documentation of test procedures and preparation of reports.
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