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Serve as the subject matter expert (SME) for all bioanalytical activities, review and approve technical documents for bioanalysis (e.g., method validation plans and reports; sample analysis reports), and assess technical capability of bioanalytical vendors to support study protocol implementation and ensure the outsourced bioanalyses are conducted with highest quality and scientific integrity in compliance with the protocol, ICH/GCP/GLP, and applicable regulatory requirements.
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Knowledge of all pertinent federal and state regulations, filing and compliance requirements, both adopted and pending, affecting employee benefits programs, including the ACA, ERISA, COBRA, FMLA, ADA, Section 125, workers' compensation, Medicare, and Social Security and DOL requirements.
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Ensure compliance with GLP, GMP, FDA, USDA, and all other regulatory requirements in accordance with company policy. They will have had demonstrated experience in strategic leadership, regulatory compliance, supplier quality management, customer satisfaction, process improvement, quality metrics and reporting, and risk management.
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Ensures compliance with all applicable federal, state, and local regulatory standards (ex TJC, DOH, FDA, HIPAA, HCFA, DPW, LCGME, SCGME, etc) Specimen management: obtain specimens for testing if applicable (including performing phlebotomy and anterior nares nasal swab collections), performs laboratory and screening tests, records results in EMR and reconciles with logs where appropriate, documents and reports findings to providers, performs all quality controls as per Point of Care Testing guidelines, prepares specimens for transport as necessary.
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Through operational expertise and industry-leading knowledge, skill, and passion, IPS provides consultancy services, architecture, engineering, project controls, construction management, and compliance services that allow clients to develop and manufacture life-impacting products.
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Maintain procurement policies and compliance standards, including third-party risk management. Maintain procurement policies and compliance standards, including third-party risk management. Experience within the BioPharma space with large molecule and vaccine CMO's.
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Join us here at Liberty Coca-Cola Beverages LLC. What would success look like? Discover what it means to be energized by a multitude of possibilities and a dynamic team. Merchandiser-Fulltime Working at Liberty Coca-Cola Beverages LLC is all about pursuing a career not just a job.
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What you’ll do: As a Jefferson Health at Home by BAYADA Physical Therapist, you’ll use your clinical skills and compassionate heart to treat patients where they want to be the most – in the comfort of their own home.
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Provide legal counsel to clients on regulatory compliance, due diligence, and real estate financing. Below covers everything you need to know about what this opportunity entails, as well as what is expected from applicants.
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Provides quality claim handling throughout the claim life cycle (customer contacts, coverage, investigation, evaluation, reserving, litigation management, negotiation and resolution) including maintaining full compliance with internal and external quality standards and state specific regulations.
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We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. Written and verbal communication skills to communicate and present tax accounting and compliance matters.
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Asist with privacy compliance including GDPR and CCPA. Support audit requests but providing appropriate documentation, data and reports needed execute. Monitor automated reports and policies for organizational compliance (SOX, NIST, backup status reports, departmental statistics, etc.
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You’ll gain exposure to environmental permitting and compliance for multiple media, including air quality, water quality, solid waste, and hazardous waste. · Oversight and preparation of compliance plans, reports, and permit applications for multiple state and federal environmental regulatory programs associated with the Clean Air Act, Clean Water Act, RCRA, EPCRA, and the Oil Pollution Prevention Act.· Conduct site visits to gather data and information and collect samples (soil, water, air) to support environmental compliance at industrial, commercial, and institutional sites.
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The Principal, Compliance and Supplier Quality is a key Supplier Quality role and reports to the Sr. Director of Compliance and Supplier Quality. Able to assess vendors quality core processes to ensure compliance with relevant guidelines and procedures.
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The Manufacturing Compliance Specialist will be responsible for helping to drive the on-time-delivery through batch closeout for all manufacturing programs, audit response and audit readiness, and other manufacturing compliance activities.
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