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Direct and assist in the development and implementation of compliance programs such as those required by DOT, EPA, OSHA, FDA, and any state-mandated programs. 2-5 years of experience with safety regulations such as OSHA, DOT, and FDA is required.
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Central Service technicians work in compliance with best practices and standards established by: The Joint Commission, AAMI, IAHSCMM, AORN, OSHA, DOT, WHO, FDA, EPA, and HIPPA.During the selection process you will participate in a virtual (pre-recorded) interview that you can complete at your convenience.
$19.09 - $26.36 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Assists in development and implementation of the environment of care program that meets current Joint Commission, Food and Drug Administration (FDA), College of American Pathologists (CAP), NFPA, and VA requirements, particularly as it relates to construction safety and infection control.
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AtriCure's Isolator Synergy Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure's AtriClip Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide.
$75,000 - $110,000 a yearFull-timeExpandUpdated 24 days ago - UpvoteDownvoteShare Job
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In support of FDA approved products, work within the Medical Science Liaison team's objectives. Provide field-based scientific exchange and communication of FDA approved and pipeline products.
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We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.
$128,300 - $150,800 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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The Food Services Shift Supervisor is responsible for directing the daily operations of an assigned kitchen unit in the County jail facilities to ensure quality and compliance to meet the USDA, FDA, and HACCP guidelines.
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Experience working with SOPs, GDP, GMP, CLIA, and the FDA. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. That’s how we tackle rare disease. By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s and.
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Works with the regional safety officer to coordinate the procedures required for compliance with OSHA, DOT, EPA, FDA, and state and local regulations and Union agreements. a) Compliance with applicable federal, state, local regulatory procedures (CGMP, DOT, OSHA, FDA.
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We are currently looking for someone who used to work for the FDA and/or has extensive experience with mock FDA Audits. SQA Services is a leading Supply Chain and Quality Assurance consulting firm specializing in the management of Supplier Audit, Quality Engineering, Inspection, and Remediation programs in the Aerospace/Defense, Semiconductor, Medical Device, Pharmaceutical, Cosmetic, and Automotive manufacturing industries.
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As a Manager Trainee - Quality with BioLife Plasma Services, a subsidiary of global leader Takeda Pharmaceutical Company, you will learn and work in a structured management training program. By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use.
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With employees in 13 states, and a 26-year partner to U.S. government agencies including the National Institutes of Health (NIH), Food and Drug Administration (FDA), Department of Homeland Security (DHS), Department of Justice (DoJ), and the Department of Commerce (DoC.
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BODYMD’S EMSCULPT NEO is the world’s only FDA cleared body sculpting procedure that burns fat and builds muscle! The ideal candidate will have a strong background in medical spa sales, pharmaceutical sales or aesthetic sales.
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Lead efforts to prepare for potential regulatory changes in the US, including the transition of our products from laboratory developed tests (LDTs) to Medical Device/In Vitro Diagnostics classification under FDA oversight.
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Work in compliance with all regulatory standards including EH&S, FDA, OSHA Radiation Safety, applicable laws, and internal policies and interpretations of the above as required. Transport packages, wooden crates, gas cylinders to and from the loading dock and mail room.
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fda job in Phoenix, AZ
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