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Administer Clinical Laboratory Improvement Amendments (CLIA)-waived rapid HIV and Hepatitis C screenings and addition to screenings for sexual transmitted infections (STI) through venipuncture blood draws and/or urine collection methods to ensure that the department is in compliance with the FDA requirements and restrictions for conducting rapid testing.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Job Summary: Control and maintain all relevant quality system documentation for dietary supplement and food manufacturing environment that comply with FDA regulations, including, SOPs, logs, forms, manufacturing records, work instructions, good documentation practices and adequacy of reference procedures and part numbers.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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As the Senior Regulatory Affairs Specialist for Stryker Sustainability Solutions, you will support vascular, surgical, and patient care product development and sustaining activities on cross-functional project teams for both US/FDA and global releases.
RemoteExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Minimum 3 years’ experience as a Software QA Lead, in an FDA (or similarly regulated) environment such as a Medical device, Pharma or Biotech domains. Strong familiarity with applicable regulations and standards including relevant FDA, CLIA, ICCBBA, AABB, FACT, ISCT, ISO and similar requirements.
ExpandApply NowActive JobUpdated 14 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.
RemoteExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Due to the requirements of this position, completion of all routine vaccinations including an FDA approved COVID-19 vaccination and annual flu shot, is mandatory prior to starting in this position, due to the constraints of the environments in which this role operates.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Ensure all plant employees are responsible and accountable to maintain GMP and site standards which include FDA, and USDA standards. At APS BioGroup, a division of Glanbia Nutritional's Inc, our portfolio centers on dairy nutritional ingredients.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Determine donor suitability by evaluating normal healthy donors for plasmapheresis procedures and immunizations that meet the criteria of normal plasma donors in accordance with DCOPs, the FDA, OSHA, CLIA and cGMP and Company policies as well as educational experience.
Part-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Food manufacturing background a plus with an understanding of FDA requirements. Experience as a maintenance or facilities technician, preferably in a manufacturing or food production environment.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Experience in development of FDA class II and III medical devices and associated solutions (pharmaceuticals), PMA products; experience in development of CE Mark class IIa, IIb, and III devices also preferred.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Our Technology support to many DoD Agencies, NASA, Voice of America, FDA, and State Agencies such as State of FL, RI, MS, ND, VA, and WV extends our delivery of solutions worldwide. Our Technology support to many DoD Agencies, NASA, Voice of America, FDA, and State Agencies such as State of FL, RI, MS, ND, VA, and WV extends our delivery of solutions worldwide.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Mobile device support including working understanding of mobile device management tools. Support large conference room Audio/Visual equipment. Our client-centric engagement model increases efficiency and effectiveness.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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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.
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Performs all aspects of the plasmapheresis procedure and plasma collection, including donor set-up, venipuncture, collects donor samples monitoring and disconnect in compliance with SOPs and FDA guidelines.
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Facilitates the research effort of the clinical research center by assisting with collection and management of data in compliance with GCP and FDA regulations. As the medical education and clinical partner of Georgetown University for more than 20 years, MedStar Health is dedicated not only to teaching the next generation of doctors, but also to the continuing education, professional development, and personal fulfillment of our whole team.
ExpandApply NowActive JobUpdated 13 days ago
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