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Knowledge of regulatory agencies standards, including but not limited to: CAP, AABB, GA DHR, Joint Commission and CLIA Ability to assist or direct the development, organization and implementation of projects, programs, and policies necessary for the operation and enhancement of the specimen procurement section.
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Develop and/or improve formulas and recipes using analytical data coming from Differential Scanning Calorimetry (DSC), Dynamic Hybrid Rheology (DHR), tempering curve analysis (Temper Index, slope, crystallization), and similar technologies.
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Under the direction of the Vegetation Management Senior (Senior Environmental Scientist, CT), the Associate Environmental Planner performs a variety of duties including research, investigations, and environmental reviews necessary for preparation of regulatory and compliance documents for various transportation and vegetation management related projects.
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I have a talented group of recruiters who specifically source Technical Sales Professionals, Scientists, Regulatory Affairs, Scientific Affairs, Executive Technical professionals, Quality Assurance, Product Development, Technical Service, Nutrition, Analytical and Corporate Chefs.
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Support and complete post market activities, including post market surveillance, regulatory reporting, and recall and correction management. Responsibilities of the Regulatory Affairs Specialist: (Included, but not limited to.
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Serves as the Title IX and Americans with Disabilities Act (ADA) Coordinator, DHR (Discrimination, Harassment, & Retaliation) Administrator and Clery Director. Leads the office in overall case management, conducts intake meetings, completes Early Resolution Agreements, oversees and/or conducts investigations of reported Title IX and DHR complaints, writes investigative reports and coordinates with campus decision makers regarding appropriate outcomes including accommodations and disciplinary action.
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Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Maintain accurate records to ensure DHR and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
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Must possess the ability to masterfully influence and manage all matters related to strategy and people operations while partnering closely with the Department of Human Resources (DHR) and collaborating and engaging internal/external stakeholders with a sense of resiliency and calmness under pressure.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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FDA regulatory experience- e.g., presenting during FDA audits, responding to regulatory inquiries, communicating directly with FDA statisticians. May develop, evaluate, implement and maintain technical quality assurance and control systems and standards pertaining to materials, techniques, or company products including ensuring a thorough connection between design controls deliverables (from design planning, requirements development, risk management, design verification/ validation through design transfer) in the DHF to process validation, production and process controls and content captured in the DHR.
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The Director of Human Resources (DHR) is responsible for directing all aspects of human resources in accordance with the policies and practices of PSI, the ethical and social consciences of business and society, and the laws, regulations, and administrative rulings of governmental organizations as well as other regulatory, advisory authorities, and organizations.
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Currently these consists of; Quality System Maintenance; Purchasing; Complaint Investigation; AM Set Up; Manual Specialty lathing; Production Control; GP ALM lathing; GP inventory management; GP inventory control; GP manual lens finishing; GP final inspection; GP invoice and packaging; GP reporting; GP lens modification; Soft Lens wet inspection; Soft Lens wet base curve / diameter inspection; Soft Lens power and surface inspection; Soft Lens incoming material processing and DHR Maintenance.
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The Senior Quality Engineer is responsible for providing quality engineering support for manufacturing on a day-to-day basis to ensure regulatory compliance. · Perform DHR Review of manufacturing performed while working on potential improvements to the overall documentation process.
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Collaborate with regulatory authorities and other stakeholders, including Fairfax Water and the Occoquan Watershed Monitoring Laboratory to ensure UOSA’s continued regulatory compliance and protection of the Occoquan Reservoir.
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Medical device, regulatory environment or pharmaceutical manufacturing is a plus. This person will collaborate with manufacturing sites and TPMs to access DHR records to perform DHR review.
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Support all initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Maintain accurate records to ensure Device History Devices (DHR) and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
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