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We are looking for an ESG Regulatory Reporting Manager to join our Finance team in North Reading. Lead compliance readiness activities for ESG regulatory reporting including the EU Corporate Sustainability Reporting Directive (CSRD), relevant SEC regulations and California's Climate Legislation, along with any additional regulatory requirements that become applicable.
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Maintain required documentation according to DDS, DMH, MassHealth, HUD, DPH, CARF and all applicable regulatory standards as well as Bridgewell policies and procedures. Provide services to individuals according to DDS, DMH, MassHealth, HUD, DPH, CARF and all applicable regulatory standards, as well as Bridgewell policies and procedures.
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Knowledge of and ability to apply environmental compliance and permitting regulations of applicable regulatory agencies, including USACE, MEPA, Massachusetts DEP, Mass CZM, local Conservation Commissions, MassDOT, and Massport.
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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application. Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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Ensures compliance with all regulatory, licensing and accreditation bodies, including but not limited to BSAS/DPH, DCF, and DMH. In conjunction with clinical leadership, ensure that all clinical services and processes are meeting or exceeding regulatory and accreditation bodies' standards.
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Responsible for the successful establishment and implementation of Records Management (RM) policies, procedures, and strategies for the way records are managed at Abiomed sites to assure compliance with J&J WWRIM Standards, regulatory and legal requirements.
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The Durable Medical Equipment (DME) Coordinator "Coordinator" is primarily responsible to ensure the ordering and securing of DME and other medical supplies for the patients at GLFHC is timely, efficient, and meets payer and other regulatory guidelines.
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Must have: A Bachelor of Science degree in Electrical/Control Engineering, Mechanical Engineering, Chemical Engineering, or Computer Science 10+ Years Work Experience Ignition & Rockwell Relevant regulatory requirements of the life science industry such as cGMP, 21 CFR Part 11, etc.
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Manage day-to-day Application Administration, user support and implementation of GxP Computerized Systems in QC Analytical Lab Manufacturing and other regulatory operations including, but not limited to, networked and non-networked standalone instruments, firmware based instruments, HMI’s, SCADA systems and any GxP application software at any manufacturing site across the North America region.
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This role collaborates with other technical organizations to set strategies for process improvements (CAPEX and OPEX) The job is critical in ensuring the site operates to PSM regulations and exceeds all corporate and regulatory EHS requirements.
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Knowledge of national and international regulatory compliances and frameworks (i.e., NIST, SOX, HIPAA, GDPR, and DFARs). Monitor regulatory compliance with enterprise security policies and educate business leaders on compliance efforts.
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Act in compliance with Heritage Healthcare's regulatory and professional standards and guidelines. The Certified Occupational Therapy Assistant (COTA) is a skilled technical worker who performs direct resident care activities under the clinical supervision of the Occupational Therapist.
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Operate Nexamp PV, Storage, and future Microgrid and Utility Scale generation assets in a manner that meets or exceeds all applicable local, state, and federal regulatory requirements. Optimize operations based on defined procedures to maximize revenues while satisfying all safety, environmental, and regulatory requirements, and to meet assigned Key Results and Key Performance Indicators.
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The Electrical Analysis - Northeast section of the Materials & Process Engineering Department is seeking an individual to fulfill the role of a Senior Electrical Failure Analysis Engineer.
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The Electrical Analysis - Northeast section of the Materials & Process Engineering Department is seeking an individual to fulfill the role of a Senior Electrical Failure Analysis Engineer.
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regulatory job Title: sr director Company: Jazz Pharmaceuticals in Andover, MA
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