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Certification in quality management (e.g., ASQ Certified Quality Auditor) or regulatory affairs (e.g., RAPS Regulatory Affairs Certification) preferred. Minimum of 5 years of experience in quality assurance and regulatory affairs within the food & beverage, dietary supplement, pharmaceutical, or related industry.
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Two years experience working in enrollment services (bursar, financial aid, registrar, housing, admissions), student services, student affairs, or a related field at a 4year, accredited institution of higher education.
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Large animal: updating and implementation of nursing curriculum, to include handling and restraint, nutrition, diagnostic and regulatory testing, wellness and preventative management, common diseases and conditions, medical and surgical care, and other areas common to large animal veterinary nursing.
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Previous skilled nursing facility experience with a solid understanding of clinical operations and regulatory compliance. The Villages at Southern Hills in Tulsa, OK has an opportunity for a Registered Nurse (RN) or Licensed Practical Nurse (LPN) to serve as Assistant Director of Nursing (ADON.
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Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist.
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As part of the Student Affairs Wellness team, Campus Recreation promotes the overall health and wellness of our entire community providing inclusive recreational and fitness opportunities. Operations and offerings reflect the needs, interests, and desires of the Pitt community while aligning with University, Student Affairs, and Campus Recreation strategic plans and revenue goals.
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It is paramount this individual has a deep understanding of Department of Veterans Affairs, Defense Health Agency, and Health and Human Services. In-depth understanding of the Department of Veterans Affairs, Defense Health Agency, and Health and Human Services.
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Summary: A Credit Specialist III assists the Managing Director of Credit Administration, Credit Specialist Lead, and Loan Processing Team ensuring compliance with the Bank’s loan policy and all regulatory requirements.
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Submit regulatory and billing related questions to HCA Corporate Regs to ensure compliance with trauma charging and billing practices. The Operations Director, under the direction of the Division Trauma Vice President, is responsible for providing strategic planning and support for initiatives and projects at the division level; including but not limited to data analysis, problem solving and coordinating the implementation of processes to assure regulatory compliance with the American College of Surgeons and the respective State Trauma designating body.
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Works in close partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the disease area leader to share information.
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In this role as a Regulatory Affairs Specialist, you will have responsibility for developing and influencing regulatory policy and determining and pursuing courses of action necessary to obtain and expand regulatory approval of Hinge Health’s medical device portfolio.
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Within the Professional Practice group, Quality and Regulatory Matters (QRM) is looking for a Technology Risk (Financial Audit IT) Senior Manager to support both US and international regulatory inspection needs as well as to serve local clients by directing engagement teams in assessing and evaluating Information Technology (IT)-related risks around clients' business systems and processes.
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Research and report safety rules established by state and federal regulatory agencies about the Department of Transportation (DOT) Pipeline and Hazardous Materials Safety Administration (PHMSA.
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Contribute directly to the growth and strategic development of a large,global Study Start-Up team;Develop and identify continuous improvement opportunities of internalprocesses;Oversee Study Start-Up/Regulatory Submissions activities and timelines toensure they are in accordance with Medpace standard operating procedures andstudy protocols;Provide input on new business development opportunities; andDevelop and maintain relationships with clients.
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Oversee the creation of technical development documentation (validation document, procedures) for new and updated Virology Division tests from research to specification required by regulatory agencies, including CAP, CLIA, FDA, Study Sponsors, and PIs.
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regulatory affairs jobs Title: regulatory affairs project Company: Glaxosmithkline in Tulsa, OK
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