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In this role, you will provide hands-on, day-to-day technical and strategic leadership and work closely with cross functional teams in Analytical Development, Process Development, Global Quality and Regulatory Affairs-CMC, and our partners in in the commercial/manufacturing to support commercialization of our company's large molecule products.
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Prepare water quality plans as required by drinking water and/or wastewater regulatory programs. Bachelor’s Degree in Environmental Science or Public Affairs. Experience working with Local, State, and/or Federal Environmental/Regulatory Agencies is a plus.
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Kimball Medical Solutions is a Medical Device Contract Manufacturer in Indianapolis, IN and the this position will report to the Quality and Regulatory Affairs Manager and have specific responsibility for a customer or several customers.
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Assists in Corporate Security and Regulatory Affairs (CSRA) training program development and training presentations related to DCP, OMP and general pharmacy operations. Also, under the general direction of the Senior Director of Corporate Security and Regulatory Affairs (Specialty), responsible for assisting in compliance and regulatory matters of Cencora's internal pharmacy and reimbursement operations.
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Stays up to date with knowledge of regulatory affairs and/or issues, including IRB, radiation safety, and Good Clinical Practices. Performs quantitative imaging outcomes for bone health and body composition using dual-energy x-ray absorptiometry and high-resolution peripheral quantitative computed tomography.
Part-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Develops professional relationships and liaise with Development, Regulatory Affairs, Technology Transfer, Office of General Counsel, Government Affairs, Research Education, Research Finance, other Research Institute departments, Division Chiefs, Department Chairs, division and hospital administrators and others as necessary on the administrative aspects of sub-awards.
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They are experts in financial structuring, engineering, construction management, and regulatory affairs, Overall, they lead the industry in comprehensive energy solutions. Comprehensive knowledge of regulatory requirements and permitting processes in renewable energy.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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You'll advise clients on their local and overseas tax affairs, while acting as a strategic consultant related to business analysis, managing indirect taxes, dispute resolution, and global enterprise tax solutions.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The position requires collaboration with other state and US government affairs team members and 3M’s government affairs team globally, as well as the company’s regulatory, legal, compliance teams as well as business and operations executives to help develop and advocate for the company’s positions on state public policy matters.
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Collaborate with cross-functional teams, including Process Development, Quality Assurance, Regulatory Affairs, and Supply Chain, to ensure alignment and compliance with regulatory requirements and company standards.
$100,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Stays up-to-date on regulatory affairs and/or clinical research best practices by attending continuing education classes, conferences, seminars, and project team meetings. Monitors study team compliance with protocol and SOPs; submits all regulatory paperwork required; communicates with PI and sub-investigators about concerns or recommended changes in study protocols, etc.
$35,651.2 - $50,003.2 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Conduct portfolio analyses to assess the performance and potential of current and future products Develop and implement product lifecycle management (PLM) strategies aligned with business objectives and market dynamics Collaborate with R&D, regulatory affairs, commercial, and supply chain teams to facilitate seamless transitions between product development phases.
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Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. The Quality Control Analyst is responsible for reviewing Medical Disability Examination ("MDE") reports and Disability Benefits Questionnaires ("DBQs") generated by medical providers for veterans evaluated on behalf of the Department of Veterans Affairs (the "VA.
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Work closely with cross-functional teams, engineers, and regulatory affairs personnel. Strong understanding of industry regulatory requirements (FDA, GMP, GAMP). Implement and maintain validation procedures per regulatory guidelines.
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Strong regulatory affairs and governance requirements for healthcare. Thorough knowledge of state and local guidelines that govern regulatory processes for healthcare. Gentiva Hospice is a member of the Gentiva family an industry leader in hospice, palliative, home health, and personal home care.
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regulatory affairs jobs in Indianapolis, UT, Massachusetts
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