Environmental Resource Specialist

Department Of Defense Pierre , SD 57501

Posted 4 weeks ago

  • Duties

Help

Duties

Summary

About the Position: The district office is located in downtown Omaha and is just blocks from the Missouri River and minutes from the city's wide array of parks, museums, historic sites, restaurants, recreation and entertainment venues such as Boys Town, the world-class Henry Doorly Zoo. Great schools, affordable housing, recreational space, and diverse activities, contribute to some of the highest standards of living in the nation. Position may be filled at any of the locations listed above.

Learn more about this agency

Responsibilities

  • Serves as the Environmental Compliance, Oil and Gas, Energy, and Sustainability Program Manager for the Omaha District Operations Division (NWO).

  • Point of contact and expert consultant for all environmental compliance, oil and gas, energy, and sustainability implementation, inspection, auditing, monitoring and reporting responsibilities and associated matters for the Division.

  • Provides staff guidance and expert policy guidance to Division staff and field offices to ensure consistent, effective, and efficient implementation of federal, state, and local environmental requirements, and sustainability matters.

  • Create sustainability program to assure compliance with applicable federal, state, and local environmental laws, regulations, and executive orders.

  • Serves as the senior natural resource specialist and District authority for implementation of the Omaha District Oil and Gas Policy.

  • The environmental program and restoration efforts require the resolution of highly complex technical problems that are further compounded by political and public interests.

Travel Required

Occasional travel - You may be expected to travel for this position up to 20%

Supervisory status

No

Promotion Potential

None

  • Job family (Series)

0401 General Natural Resources Management And Biological Sciences

  • Requirements

Help

Requirements

Conditions of Employment

  • Appointment may be subject to a suitability or fitness determination, as determined by a completed background investigation.

  • Must have and maintain a valid state driver's license.

  • Must have completed a 40-hr Hazardous Waste Operations and Emergency Response (HAZWOPER) course and maintained annual HAZWOPER refresher certifications. Annual refreshers must be maintained throughout the performance of work under this position.

Qualifications

Who May Apply: Only applicants who meet one of the employment authority categories below are eligible to apply for this job. You will be asked to identify which category or categories you meet, and to provide documents which prove you meet the category or categories you selected. See Proof of Eligibility for an extensive list of document requirements for all employment authorities.

  • Current Department of Army Civilian Employees

  • Current Permanent Department of Defense (DOD) Civilian Employee (non-Army)

  • Domestic Defense Industrial Base/Major Range and Test Facilities Base Civilian Personnel Workforce

  • Interagency Career Transition Assistance Plan

  • Land Management Workforce Flexibility Act

  • Military Spouses, under Executive Order (E.O.) 13473

  • Non-Department of Defense (DoD) Transfer

  • People with Disabilities, Schedule A

  • Priority Placement Program, DoD Military Spouse Preference (MSP) Eligible

  • Reinstatement

  • Veterans Employment Opportunity Act (VEOA) of 1998

In order to qualify, you must meet the education and or experience requirements requirements described below. Experience refers to paid and unpaid experience, including volunteer work done through National Service programs (e.g., Peace Corps, AmeriCorps) and other organizations (e.g., professional; philanthropic; religious; spiritual; community; student; social). You will receive credit for all qualifying experience, including volunteer experience. Your resume must clearly describe your relevant experience; if qualifying based on education, your transcripts will be required as part of your application. Additional information about transcripts is in this document.

Basic Requirement for Environmental Resources Specialist

A. Degree: Bachelor's degree (or higher degree) in biological sciences, agriculture, natural resource management, chemistry, or related disciplines appropriate to the position.

OR

B. Combination of Education and Experience: Courses equivalent to a major in zoology, or in a related discipline that included course work as shown in A above, plus appropriate experience or additional education.

In addition to meeting the basic requirement above, to qualify for this position you must also meet the qualification requirements listed below:

Specialized Experience: One year of specialized experience which includes 1. Environmental stewardship programs and associated development of leasable minerals (oil and gas); and 2. Expertise in the areas of natural resources and environmental science principles leading to the execution of an environmental compliance program including prevention, protection, and reclamation efforts dealing with Environmental Stewardship of project lands. This definition of specialized experience is typical of work performed at the second lower grade/level position in the federal service (GS-12).

You will be evaluated on the basis of your level of competency in the following areas:

  • Environmental Law and Regulatory Compliance

  • Natural Resource Management

  • Planning and Evaluating

  • Project Management

Time in Grade Requirement: Applicants who have held a General Schedule (GS) position within the last 52 weeks must have 52 weeks of Federal service at the next lower grade or equivalent (GS-12).

Education

FOREIGN EDUCATION: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university. For further information, visit: http://www.ed.gov/about/offices/list/ous/international/usnei/us/edlite-visitus-forrecog.html

icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Senior Staff Regulatory Affairs Specialist

Stryker Corporation

Posted 1 week ago

VIEW JOBS 10/18/2020 12:00:00 AM 2021-01-16T00:00 Job Description Stryker is one of the world's leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Staff Regulatory Affairs Specialist to join our Neurovascular Division to be based in Fremont, CA preferably or anywhere within the United States. Stryker's Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions. The business is dedicated to providing innovative stroke products and services for ischemic and hemorrhagic stroke and committed to providing clinical education and support to help physicians deliver better patient outcomes. Products include: stent retrievers, detachable coils, stents, balloons, guidewires and microcatheters. In February 2019, Stryker Corporation (NYSE:SYK) announced that for the ninth consecutive year has been named as one of the FORTUNE 100 Best Companies to Work For ranking 11 out of 100. If you join our organization; will be working to "Make Stroke History". Stroke is devastating; 1 of 20 deaths is from a stroke, according to the CDC. Watch this video to see how Stryker is making a difference: [ Link removed ] - Click here to apply to Senior Staff Regulatory Affairs Specialist. Who we want * Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities. * Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions. * Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues. * Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. * Curious learners. People who seek out cutting-edge research and information to expand and enhance their ability to develop new ideas into reality. What you will do As the Senior Staff Regulatory Affairs Specialist, you will be responsible to prepare complex submission to gain approvals for clinical studies and commercial distribution in in one or more of the following geographic regions: United States, Europe, Japan, Canada, and other international countries. * Assess regulatory intelligence to assist in the development of local, regional, and global regulatory strategies. * Evaluate the regulatory environment and contributes to providing internal advice throughout the product lifecycle (e.g., concept, development, manufacturing, marketing) to ensure product compliance. * Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. * Identify the need for new regulatory procedures, SOPs, and participates in development and implementation. * Help train stakeholders on current and new regulatory requirements to ensure organization-wide compliance. * Assist other departments in the development of SOPs to ensure regulatory compliance. * Provide regulatory input and technical guidance on global regulatory requirements to product development teams. * Advise stakeholders of regulatory requirements for quality, preclinical, and clinical data to meet applicable regulations. * Assess the acceptability of quality, preclinical, and clinical document for submission filing to comply with applicable regulations. * Evaluate proposed preclinical, clinical, and manufacturing changes for regulatory filing solutions and proposes plans/strategizes (if appropriate) for changes that do not require submissions. * Provide knowledge and guidance on preapproval inspections, GCP inspections, and clinical investigator relationships. * Identify, monitor and submit applicable reports or notifications to regulatory authorities during the clinical research process. * Provide regulatory information and guidance for proposed product claims/labeling. * Communicate and interacts with regulatory authorities before and during the development and review of a regulatory submission through appropriate communication tools. * Work with cross-functional teams for interactions with regulatory authorities including panel meetings and advisory committees. What you need * A Bachelor's Degree (B.S or B.A) in Engineering, Science or equivalent focus is required. * A minimum of 7 years of experience in an FDA regulated industry required; preferably with medical devices. * A minimum of 5 years of Regulatory Affairs experience required. * RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. * General understanding of product development process and design control. * Understanding of regulations applicable to the conduct of clinical trials required. * Thorough understanding of FDA and international medical device regulations. * Previous experience with Class III medical devices required. * Previous experience drafting an IDE/PMA submission required. * RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred. * Experience interacting with regulatory agencies preferred. * Knowledgeable in areas such as regulatory pathways; risk-benefit analysis; communication and collaboration internally and externally; submission, registration, obtaining approval, documentation, compliance, post marketing surveillance/vigilance; and distribution. * Ability to comply with constantly changing regulatory procedures and prioritize work effectively. * Ability to analyze and resolve non-routine regulatory issues using independent judgment. * Excellent analytical and writing skills. * Excellent interpersonal, written and oral communication skills. * Effective organizational skills. * Advanced PC skills with proficiency in Microsoft office Suite, including Excel. Work From Home: Remote Travel Percentage: 20% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. Stryker Corporation Pierre SD

Environmental Resource Specialist

Department Of Defense