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High school diploma or equivalent with three years or more meat and/or seafood industry (as appropriate) FSQA Leadership experience at a federal CFIA/FDA meat and/or seafood processing plant, or a Bachelor's degree in Animal Science, Food Science, or Biological Science from four-year college or university with one or more years meat and/or seafood industry (as appropriate) FSQA Leadership at a federal CFIA/FDA meat and/or seafood processing plant.
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Must have knowledge and understanding of OSHA, NFPA, The Joint Commission, CAHO, EOC, FDA and other specific regulations and standards pertaining to clinical equipment service and repair. Provides assistance and training to Bio-Medical Equipment Technician I as assigned by Clinical Engineering Management.
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The Senior Scientist I role is a non-supervisory position that is responsible for development, evaluation, qualification, and validation of methods and testing of reference materials to support development and maintenance of USP standards and tools.
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Evaluate and validate the performance of analytics using standard techniques and metrics (e.g. cross validation, ROC curves, confusion matrices) About Avid Technology Professionals Avid Technology Professionals, LLC (ATP) is a premiere provider of software and systems engineering, and acquisition program management services for the community.
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Certification demonstrates knowledge and skills of sterile processing practices in accordance with regulatory guidelines such as Food and Drug Administration (FDA) and the Joint Commission (JC.
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Ensures the Infection Prevention and Control Program complies with the guidelines and recommendations of the CDC, EPA, FDA, OSHA, or other relevant agencies. Maintain patient safety program requirements/validation criteria.
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This individual will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.
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Knowledge of regulations, policies and reporting relevant to the protection of human subjects in clinical trials: GCP, IRB, FDA, SAE reporting, IND applications. 3 + years of experience in clinical research and/or bioethics with preferred experience directly related to safety & pharmacovigilance.
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The Senior Integration and Test Engineer will be responsible for developing and maintaining system verification and validation plans of the Telesat Lightspeed constellation communication system.
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One to 3 years of meat and/or seafood industry (as appropriate) experience at a federal CFIA/FDA meat and/or seafood processing plant (as appropriate). Formal job training in TQM principles, SPC, HACCP concepts, CFIA/FDA regulations would be beneficial.
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You will also support internal Risk Adjustment Data Validation (RADV) monitoring programs and audits, interpret statistical analyses to enhance quality and population health, and collaborate with provider leadership to maintain and enhance risk adjustment accuracy.
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Must have knowledge and understanding of OSHA, NFPA, The Joint Commission, EOC, FDA and other specific regulations and standards pertaining to clinical equipment service and repair. Must have a basic understanding of anatomy, physiology, and medical terminology.
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Support microbiology technology validation and implementation for testing pharmaceutical products and manufacturing environment. Facilitate method transfer, validation, and implementation of new microbiology technologies at secondary commercial sites.
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General Dynamics Information Technology is seeking to fill an IT O&M Delivery Manager , role on an existing contract to support the Food and Drug Administration (FDA) and their critical mission needs.
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We are hiring an experienced Validation Engineer to support multiple commissioning, qualification, and validation projects. 5+ years in a equipment commissioning, qualification, and validation engineering role, including proven success developing and executing validation protocols in the pharmaceutical manufacturing industry.
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fda validation jobs in Rockville, MD
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