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  1. SENIOR ANALYST - REGULATORY AFFAIRS at Stifel Nicolaus

    Actively coordinates and directs the Firm regulatory exams, regulatory inquires and sweeps including research, validating data, pre-work, on-site requests,...

  2. Government Relations Specialist at Sublime Wireless

    Will also be called upon to interface with external staff on matters related to municipal codes and to effectively communicate regulatory status in support of...

  3. International Regulatory Affairs Specialist at Becton Dickinson & Company

    Job Regulatory Affairs Primary Location US-Maryland-Baltimore Shift First Shift / Day Job Relocation Available No....

  4. Regulatory Affairs Specialist at Sterling Hoffman Life Sciences

    Prepare clinical regulatory documents when needed. Ensure that regulatory submission timelines for assigned projects are met....

  5. Business Analyst/Sr Business Analyst (BGE) at Exelon Corporation

    POSITION SPECIFICATIONSMinimum-Business AnalystBachelors degree in Business or Engineering AND 2 - 5 years related business experience, or in lieu of Bachelors...

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    1. CMC Regulatory Manager

      Our client, a leading biopharmaceutical company, is currently recruiting a CMC Regulatory Manager to provide leadership and energy to its regulatory management team. This is an exceptional opportunity to join a corporate culture known for its innovative and growth-oriented vision. Responsibilities include: 1) Prepare regulatory submissions that are compliant with FDA and international ...

    1. PROGRAM SUPPORT ASSISTANT, GS-303-7 at U.S. Department of State

      This position is located in the Department of Health and Human Services (DHHS), Food and Drug Administration (FDA), Office of Regulatory Affairs, Office of...

    1. Regulatory Affairs Specialist

      Our client, a leading pharmaceutical company, is currently seeking a driven and ambitious Regulatory Affairs Specialist to join their team. This is a unique opportunity for a highly motivated professional who has a go-getter attitude. 1) Prepare scientific and regulatory documents (e.g. clinical protocols, investigator’s brochures, informed consent forms, annual reports, investigational new ...

    1. Supervisory Public Affairs Specialist at U.S. Department of State

      Supervisory Public Affairs Specialist. As a Supervisory Public Affairs Specialist you will be responsible for the following duties:....

    1. Senior Regulatory Affairs Specialist

      Our client, a leading pharmaceutical company, is currently seeking a driven and ambitious Senior Regulatory Affairs Specialist to join their team. This is a unique opportunity for a highly motivated professional who has a go-getter attitude. 1) Prepare regulatory submissions to ensure compliance with FDA and international regulations and guidelines at the guidance of the Regulatory Affairs ...

    1. Legislative Affairs Specialist at Constellation West

      Familiar with legislative and regulatory documents and have a working knowledge of the legislative and regulatory process....

    1. Manager Regulatory Affairs

      We have a great opportunity for a Senior Regulatory Affairs Manager with a top medical device company in southern Pennsylvania. Looking for experience with US and Canada regulatory activities. This includes, but not limited to experience with Premarket Approval (PMAs) and supplement (sPMA), Investigational Device Exemption (IDE), and Premarket Notification ( 510[k] ) applications. Drug ...

    1. Financial Center Specialist at USAA

      May work Military Affairs and Grassroots marketing events. Adheres to all regulatory and compliance policy and procedures....

    1. Remote Clinical Project Manager

      Hello, My name is Christina and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Clinical Project Manager for a prominent client of ours.  This position is located in Gaithersburg, MD. Details for the position are as follows: Job Description:Plan and manage overall clinical operations for assigned clinical trial(s)/projects including timelines, ...

    1. JPEO CBD COMMUNICATIONS SPECIALIST at Engility Corporation

      The contractor’s expert knowledge shall include the ability to establish and maintain an effective working relationship with media representatives, public...

    1. Regulatory Affairs Manager

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Regulatory Affairs ManagerJob ID: 2402Industry: Biotech/PharmaceuticalLocation: Gaithersburg, MDDuration: 12 monthsHours per Week: 40 Responsibilities: Description- Prepare ...

    1. Chief Security Architect at General Dynamics Information Technology

      Strong working knowledge of regulatory and statutory security requirements such as HIPAA, NIST, FISMA, DIACAP, ISO 27001+....

    1. Therapeutic Area Lead - Chronic Inflammation Disorders

      Seeking experienced Medical Affairs Director with strong background in Phase IV clinical trials, brand strategy development and product lifecycle management. Shall: *** Lead the Medical Affairs team involved in post marketing commitments such as Phase IV clinical studies. *** Develop, approve and oversee medical education programs for team members, investigators, Key Opinion Leaders and ...

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      No Telecommute

    1. Medical Care Coordination Senior Social Worker at U.S. Department of State

      Department Of Veterans Affairs. Veterans Affairs, Veterans Health Administration. For more information on the Department of Veterans Affairs....

    1. Regulatory Affairs Manager (contract - local candidates)

      Description- Prepare and deliver regulatory operational plans for allocated projects/products. Contribute to solutions to regulatory issues. Project manage quality regulatory submissions to agreed project targets. Provide operational regulatory input and guidance in cross-functional teams. Work flexibly within and across Therapeutic Areas to provide broad regulatory support to ensure the ...

    1. Network Real Estate Specialist (Multiple Openings) at Crown Castle

      Three (3) to five (5) y e a r s p r o v en e x pe ri en c e wo r k i ng for a wireless carrier, regulatory/governmental/external affairs consulting firm, a u t...

    1. Business Development Manager

      Maxim Healthcare Services is one of the leading providers of medical staffing, home health and wellness services in the United States. Founded in 1988, Maxim has rapidly expanded to include 12 divisions and over 400 branch offices in 44 states and the District of Columbia. We have earned a position as an innovative leader in the healthcare industry through our emphasis on patient care and ...

    1. Dietitian at U.S. Department of State

      Department Of Veterans Affairs. Veterans Affairs, Veterans Health Administration. Ability to comply with various accrediting, regulatory, and agency authorities...

    1. Regulatory Affairs Specialist

      Kelly Scientific Resources along with a leading pharmaceutical company in Wilmington, DE and Gaithersburg, MD have an immediate need for a Regulatory Affairs Specialist.JOB DESCRIPTION: Prepares/agrees/executes global/regulatory tactical submission plans for allocated project/prod that implement the agreed regulatory strategy to develop and maintain products. Provides independent tactical ...

    1. Program Assistant -- Academic Affairs at Loyola University Maryland

      This position provides support for the coordination, planning and facilitation of key academic events and ceremonies (including Honors weekend and Commencement...

      1. Senior Regulatory Affairs Specialist at Sterling Hoffman Life Sciences

        Assist Regulatory Affairs Director as needed. Prepare regulatory submissions to ensure compliance with FDA and international regulations and guidelines at the...

      2. Animal Originated Tissue Expert at Tuv America

        Perform evaluations of regulatory submissions including:. Perform regulatory audits of clients per European Medical Device Directives (AIMD, MDD, IVDD),...

      3. Prin Medical Writer at Medtronic

        Collaborate with regulatory teams on all phases of regulatory submissions and approvals, including clinical document preparation and review, regulatory document...

      4. Clinical Study Design Specialist II at IDEXX Laboratories

        Familiarity with regulatory processes, clinical research processes and standards. Works with medical affairs and others to establish/refine study scope...

      5. Business Analyst/Sr Business Analyst (BGE) at Exelon

        Comprehensive understanding of applicable standards, methods, processes and practices, business fundamentals, and performance metrics in the specific functional...