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The Federal Regulatory Affairs Manager will collaborate closely with the North America Team Leader and business-lead Vice Presidents to develop regulatory strategies to ensure registrations are obtained and maintained to meet business objectives and timelines.
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Regulatory Compliance: Ensure all sales activities and client solutions comply with local, state, and federal environmental regulations, including RCRA, CERCLA, and DOT requirements. Market Analysis: Monitor industry trends, competitor activities, and regulatory changes to identify new business opportunities and adapt sales strategies accordingly.
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Experience in drinking water system water quality and regulatory compliance including; LCRR experience, implementation of water quality treatment improvements and corrosion control strategies, regulatory agency negotiations, and public outreach programs.
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Communicate with in-house counsel and internal compliance to ensure enforceability of documentation and regulatory compliance. Assist Application and Data Services with: Maintaining CSI templates and libraries to ensure compliance with bank policies and regulatory requirements.
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Support external client audits; perform periodic walk-through audits of Analytical Development and Quality Control laboratories; Support regulatory (FDA, EMA) and client audits/inspections of Catalent.
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Monitors trends and analyzes grievance and appeals data to identify and recommend plan and policy changes and to ensure state and federal regulatory compliance and resolution within the regulatory timeframes.
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Continually evaluate systems and procedures for improvement for efficiency and compliance to applicable regulatory requirements and standards; Work independently under general supervision to meet company goals; actively participates in training activities, managing their individual training plan.
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As a Bilingual Construction Safety Specialist, you will be responsible for providing field support services and assisting managers, supervisors, and team members with implementing specific Company and Client Safety and Health policies and procedures, regulatory compliance, and continual improvement of the overall performance of the Company in a manner that is consistent with the Company s Core Values.
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). We assist companies and non-profit organizations in delivering benefits to their employees.
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The Clinical Pharmacist is a licensed professional who is responsible for providing safe and appropriate pharmacy services to Option Care patients in accordance with the policies and procedures of the Option Care, pharmacy practice professional standards, and applicable regulatory entities.
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Ensures compliance with the Joint Commission, State Health Department, EPA, DEP, ADA, UST, and other regulatory business appointments. Certified Health Care Facility Manager (CHFM) preferred. Ensures compliance with the Joint Commission, State Health Department, EPA, DEP, ADA, UST, and other regulatory business appointments.
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Act as a clinical resource for perioperative personnel using current literature and guidelines, organizational policies and procedures, and regulatory and accreditation standards. We have pioneered a physician-led, multi-site model of practice solutions that restores physician agency by aligning incentives to support growth and transition to value-based care.
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Develop and oversee handling procedures for sensitive information and establish new accountability processes unique to NATO Regulations and Accountability practices for JHU/APL. Manage all APL Staff with a Personal Security Clearance Level (PCL) & valid Need-to-Know (NTK) for access NATO Classified Material are vetted with the appropriate NATO Accesses and that the accesses are renewed annually per NATO regulatory requirements.
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As an Back-End Pharmacy Technician, you will work to ensure all medication needs and regulatory standards are met for our patients. Rotating and working in various assigned pharmacy workstations including: Packaging, Staging, Returns, Receiving, Narcotics, IV, Ekit, Compounding, Omnicell Cycle Fill, Machine Packaging.
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This fully remote position will be responsible for providing regulatory and compliance advice on a day-to-day basis to the Johns Hopkins Medicine Institutional Review Boards (JHM IRBs). The Associate will lead regulatory consults with faculty to assist with protocol planning and addressing complex regulatory issues that may arise as part of the IRB submission and review process.
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regulatory job in Columbia, MD
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