Regulatory Specialist ( Sample Clauses

Regulatory Specialist (. Key Personnel). The Regulatory Specialist is responsible for assuring that the Contractor achieves regulatory compliance during all environmental related activities in the task order. The Regulatory Specialist must have professional knowledge, thorough understanding, and applied practical experience dealing with environmental regulations including, but not limited to, RCRA, CERCLA, Superfund Amendments & Reauthorization Act (XXXX), Toxic Substances Control Act (TSCA), Clean Air Act, Clean Water Act, and implementing Federal, State, and local regulations and their application to projects. Regulatory Specialist shall have a Bachelor’s degree from an accredited college or university in a relevant field, four (4) years of relevant experience and/or training, or an equivalent combination of relevant education and experience. In order to qualify without a college degree, Regulatory Specialist shall have a minimum of 12 years relevant experience. Regulatory Specialist shall be an employee of the prime Contractor.
Sample 1Sample 2Sample 3See All (4)
AutoNDA by SimpleDocs
Regulatory Specialist (. The Regulatory Specialist is responsible for assuring regulatory compliance is achieved for all environmental related activities in the task order. The project Regulatory Specialist should have professional knowledge of, thorough understanding of and applied practical experience of environmental regulations with respect to RCRA, CERCLA, the Hazardous Materials Conservation Act, the Superfund Amendments & Reauthorization Act (XXXX), the Toxic Substances Control Act (TOSCA), the Clean Air Act, the Clean Water Act, DOT regulations, etc., and implementing federal, state and local regulations and their application to the projects. • The individual proposed as the Regulatory Specialist shall have a college degree in physical, natural or environmental sciences, engineering from an accredited 4-year program. • The individual proposed as the Regulatory Specialist shall be a current Certified Hazardous Materials Manager (CHMM). • The individual proposed as the Regulatory Specialist should have a minimum of five (5) years of professional experience related to ERS • The individual proposed as the Regulatory Specialist should have a minimum of three (3) years specialized experience in the accumulation, manifesting and shipment of wastes. The Regulatory Specialist shall demonstrate the completion of HAZWOPER training and other applicable training (as required to maintain compliance) and will be required to maintain/refresh training during the life of the contract in accordance with the regulations.
Sample 1Sample 2
Regulatory Specialist (. The Regulatory Specialist is responsible for assuring regulatory compliance is achieved for all environmental and transportation related activities in the Task Order. The project Regulatory Specialist must have professional knowledge of, thorough understanding of, and applied practical experience of environmental regulations with respect to RCRA, CERCLA, the Hazardous Materials Transportation Act, the Superfund Amendments & Reauthorization Act (XXXX), the Toxic Substances Control Act (TSCA), the Clean Air Act, the Clean Water Act, etc., and implementing federal, state and local regulations and their application to the projects. The Regulatory Specialist shall have a college degree in environmental, physical or natural sciences or in engineering, shall have professional registration in their respective field of expertise (e.g., Registered Professional Engineer (PE); Certified Hazardous Materials Manager (CHMM); Registered Environmental Manager (REM), or equivalent), and a minimum of three
Sample 1
Regulatory Specialist (. The Regulatory Specialist is responsible for assuring regulatory compliance is achieved for all environmental related activities in the task order. The project Regulatory Specialist must have professional knowledge of, thorough understanding of, and applied practical experience of environmental regulations with respect to RCRA, CERCLA, the Hazardous Materials Conservation Act, the Superfund Amendments & Reauthorization Act (XXXX), the Toxic Substances Control Act (TSCA), the Clean Air Act, the Clean Water Act, etc., and implementing federal, state and local regulations and their application to the projects. The Regulatory Specialist shall have a college degree in environmental, physical or natural sciences or in engineering, shall have professional registration in their respective field of expertise (e.g. Certified Hazardous Materials Manager (CHMM); Registered Environmental Manager (REM), or equivalent.), and a minimum of three (3) years’ experience in the accumulation, manifesting, and shipment of hazardous, toxic, and if required by the task order, radiological wastes. Depending upon the task order requirements, the Regulatory Specialist shall be able to demonstrate the completion of the following training and will be required to maintain/refresh training during the life of the contract in accordance with the regulations:  Training and current certification under 49 CFR 172, Subpart H. If a DOT security plan is required, the Contractor shall be in full compliance with DOT regulation, 49 CFR, Subchapter C, Subpart I.
Sample 1

Related to Regulatory Specialist (

  • Specialist A dentist who focuses on a specific area of dentistry, including oral surgery, endodontia, periodontia, orthodontia and pediatric dentistry, or a group of patients to diagnose, manage, prevent or treat certain types of symptoms and conditions. Spouse: The person to whom the Subscriber is legally married, including a same sex Spouse. Spouse also includes a domestic partner. Subscriber: The person to whom this Contract is issued. UCR (Usual, Customary and Reasonable): The cost of a dental service in a geographic area based on what Providers in the area usually charge for the same or similar medical service. Us, We, Our: BlueShield of Northeastern New York and anyone to whom We legally delegate performance, on Our behalf, under this Contract. Utilization Review: The review to determine whether services are or were Medically Necessary or experimental or investigational (including treatment for a rare disease or a clinical trial). You, Your: The Member.

  • REGULATORY FILINGS AND CAISO TARIFF COMPLIANCE 3.1 Filing

  • Regulatory Reporting Ultimus agrees to provide reports to the federal and applicable state authorities, including the SEC, and to the Funds’ Auditors. Applicable state authorities are those governmental agencies located in states in which the Fund is registered to sell shares.

  • Development cooperation 1. The Parties recognise that development cooperation is a crucial element of their Partnership and an essential factor in the realisation of the objectives of this Agreement as laid down in Article 1. This cooperation can take financial and non-financial forms.

  • Investigational Services This plan covers certain experimental or investigational services as described in this section. Clinical Trials This plan covers clinical trials as required under R.I. General Law § 27-20-60. An approved clinical trial is a phase I, phase II, phase III, or phase IV clinical trial that is being performed to prevent, detect or treat cancer or a life-threatening disease or condition. In order to qualify, the clinical trial must be: • federally funded; • conducted under an investigational new drug application reviewed by the Food and Drug Administration (FDA); or • a drug trial that is exempt from having such an investigational new drug application. To qualify to participate in a clinical trial: • you must be determined to be eligible, according to the trial protocol; • a network provider must have concluded that your participation would be appropriate; and • medical and scientific information must have been provided establishing that your participation in the clinical trial would be appropriate. If a network provider is participating in a clinical trial, and the trial is being conducted in the state in which you reside, you may be required to participate in the trial through the network provider. Coverage under this plan includes routine patient costs for covered healthcare services furnished in connection with participation in a clinical trial. The amount you pay is based on the type of service you receive. Coverage for clinical trials does not include: • the investigational item, device, or service itself; • items or services provided solely to satisfy data collection and that are not used in the direct clinical management; or • a service that is clearly inconsistent with widely accepted standards of care.

  • Manufacturer's Recommendations All work or materials shall be installed in accordance with the manufacturer's recommendations and requirements. The Contractor shall obtain the manufacturer’s recommendations and requirements, for its use at the Site in executing the Work, copies of bulletins, circulars, catalogues, or other publications bearing the manufacturer’s titles, numbers, editions, dates, etc. If the manufacturer’s recommendations and requirements are not available, the Contractor shall request installation instructions from the Design Professional.

  • Regulatory Filing In the event that this Interconnection Construction Service Agreement contains any terms that deviate materially from the form included in Attachment P or from the standard terms and conditions in this Appendix 2, the Transmission Provider shall file the executed Interconnection Construction Service Agreement on behalf of itself and the Interconnected Transmission Owner with FERC as a service schedule under the Tariff. Interconnection Customer may request that any information so provided be subject to the confidentiality provisions of Section 17 of this Appendix

  • Statewide HUB Program Statewide Procurement Division Note: In order for State agencies and institutions of higher education (universities) to be credited for utilizing this business as a HUB, they must award payment under the Certificate/VID Number identified above. Agencies, universities and prime contractors are encouraged to verify the company’s HUB certification prior to issuing a notice of award by accessing the Internet (xxxxx://xxxxx.xxx.xxxxx.xx.xx/tpasscmblsearch/index.jsp) or by contacting the HUB Program at 000-000-0000 or toll-free in Texas at 0-000-000-0000.

  • Surgery Services and Mastectomy Related Treatment This plan provides benefits for mastectomy surgery and mastectomy-related services in accordance with the Women’s Health and Cancer Rights Act of 1998 and Rhode Island General Law 27-20-29 et seq. For the member receiving mastectomy-related benefits, coverage will be provided in a manner determined in consultation with the attending physician, physician assistant, or an advance practice registered nurse and the patient, for: • all stages of reconstruction of the breast on which the mastectomy was performed; • surgery and reconstruction of the other breast to produce a symmetrical appearance; • prostheses; and • treatment of physical complications at all stages of the mastectomy, including lymphedema. See the Summary of Medical Benefits for the amount you pay.

  • Geotechnical Engineer « »« » « » « » « » « »

Time is Money Join Law Insider Premium to draft better contracts faster.