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regulatory affairs in Los Angeles

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  1. Coordinator, Decedent Affairs Services at St. Francis Medical Center

    Manages all aspects of Decedent Affairs for hospital. Ensures compliance with regulatory requirements and legal documentation requirements....

  2. Manager Clinical Development Dermatology at Allergan

    Knowledge of regulatory requirements and GCPs required. This includes responsibility for the clinical team's creation of relevant documents and outputs...

  3. Regulatory Affairs Director at OASIS Medical Inc.

    Regulatory Affairs Director*. The Regulatory Affairs Director is responsible for regulatory compliance, product registration, labeling, and advertising...

  4. Director Regulatory Affairs at Advanced Personnel Profiles, Inc.

    S/he will need to identify, assess and communicate regulatory development and submission strategies, regulatory risks, interface with relevant regulatory...

  5. Senior Manager, Payor Negotiation and Fees at Pacific Dental Services

    And work with PDS team members on regulatory and legislative affairs. Senior Manager, Payor Negotiation & Fees....

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    1. Regulatory Affairs Associate (4243)

      . Regulatory Operations team member in the Authoring Support Group (ASG) responsible for formatting of regulatory submission documents ensuring that documentation meets Shire’s submission-ready standards under direct supervision.Essential Duties and Responsibilities:This section contains a list of five to eight primary responsibilities of this role that account for 5% or more of the work. The ...

    1. Clinical Quality Assurance Professional at W. L. Gore & Associates

      Participating in Clinical Affairs Process Improvement initiatives. Serving as a primary contact for regulatory inspections....

    1. Regulatory Affairs Specialist

       Summary: Regulatory Operations team member in the Authoring Support Group (ASG) responsible for formatting of regulatory submission documents ensuring that documentation meet our clients submission-ready standards under direct supervision. Responsibilities: ·         Convert MS Word documents in a legacy format to ISIWriter using a custom conversion tool, ensuring that the correct styles and ...

    1. Senior Clinical Research Operations Specialist at Chiltern International

      Interface with Regulatory Affairs to obtain regulatory document approval for clinical study sites; Coordinate site regulatory document collection for assigned...

    1. Document Control Technician

       The Document Control Technician is responsible for processing and maintaining all controlled documents in regulatory affairs. Responsibilities include creating, editing, indexing, tracking, and storage of documents as cGMP guidelines.Responsibilities: Issuance of approved SOP’s and maintain a log of all SOP’s on the floor.File and maintain SOP's, Master and executed batch records, packaging, ...

    1. Product Monitoring Specialist (Men/Women) based in Saint louis at Guerbet

      Work in conjunction and effectively communicate with cvarious departments, including legal Affairs, Regulatory Affairs, R&D, Marketing, Medical Affairs, Sales...

    1. Director Regulatory Affairs

      Overview: As part of the leadership team the Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies for Class II/III medical devices This individual will be the Regulatory subject matter expert for all applicable medical devices. S/he will need to identify, assess and communicate regulatory development and submission strategies, ...

    1. LIMS SME/Business Analyst at LabAnswer

      The LIMS SME/Business Analyst will provide support for an enterprise StarLIMS implementation for the Food and Drug Administration (FDA) Office of Regulatory...

    1. Regulatory Affairs Specialist

      Primary Responsibility / SummaryA regulatory affairs specialist assists in the implementation of international and domestic regulatory strategies. Help with the preparation, coordination, and compiling of applications to foreign and domestic regulatory agencies. Effectively lead and provide regulatory guidance, in addition to deliver the global regulatory strategy for product development and ...

    1. Chief Medical Officer (Physician) at Department of Veterans Affairs

      Achieve corporate objectives in quality of services and programs throughout the VISN as evaluated by internal indicators, regulatory reviews and accreditation...

    1. Sr. Associate Regulatory Affairs (CMC)

      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: Sr. Associate Regulatory AffairsJob ID: 2305Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 1 year contractPay Rate Range: Depends on Experience (W-2 all ...

    1. Clery Compliance Manager (Recruitment #60137) at California State University

      In addition, the Vice President works closely with the Provost and Academic Affairs Vice President, the Vice President for Student Affairs, the Chief...

    1. Regulatory Affairs Specialist

      Quest is seeking a Regulatory Affairs Specialist who will be responsible for successfully implementing and scaling the company’s global regulatory and compliance program to support bringing our products to the market globally. The role will ensure that Quest is in compliance with all applicable domestic and international laws, regulations and customs for key markets at both the ingredient and ...

    1. Director of Environmental Health and Safety (Job ID 5521) at CSU Northridge

      Academic Affairs, College of Science and Math and others, Administration and Finance, Student Affairs, Student Health Center, Athletics, Extended Learning,...

    1. Clinical Affairs Manager

       Job DescriptionThe Clinical Affairs position will assist the Clinical Affairs Director in planning, coordinating and completing studies. The candidate needs to have excellent communication and presentation skills, together with the ability to organize and motivate others. The candidate must demonstrate enthusiasm, innovation and leadership when faced with challenges and will provide ...

    1. Counsel, Business and Legal Affairs at Television Production Company

      Counsel, Business & Legal Affairs*. Minimum 3 years of relevant experience at entertainment law firm, media entertainment company, and/or business affairs...

    1. Sr Associate, Software Labeling Lead (Regulatory)

      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: Senior Associate Software Labeling LeadJob ID: 2419Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 11 Month ContractPay Rate Range: Depends on Experience ...

    1. Senior Specialist, Regulatory Affairs at Allergan, Inc.

      The Senior Specialist –Regulatory Affairs with supervision, reviews, plans and prepares routine and complex regulatory submission documents for regulatory...

    1. Clinical Research Associate

       Clinical Research Associate (contract) LOCATION: Los Angeles, CA POSITION SUMMARY: Responsible for site management and performance (including documentation) of on-site monitoring (all types of visits) activities for multiple investigational sites in accordance with designated project assignments, (SOPs), Good Clinical Practices (GCPs) and applicable regulatory requirements. SPECIFIC DUTIES ...

    1. MEDICAL STAFF COORDINATOR at Los Angeles County Department of Human Resources

      Conducts routine internal audits of the review process to ensure compliance with regulatory agencies; Supports various Committees by working closely with the...

    1. Clinical Research Associate (Contract)

      Job Title: Clinical Research Associate  LOCATION: Santa Clarita, CA POSITION SUMMARY The CRA is responsible for the execution of moderately complex human clinical research studies in compliance with corporate policies and procedures, Good Clinical Practices and all applicable laws and regulations. The CRA, with supervisory direction, must effectively manage multiple clinical sites to assure ...

    2. Principle IS Business Systems Analyst

      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: Principal IS Business Systems AnalystJob ID: 2406Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 5-6 Month Contract, with possible extensionPay Rate ...

    3. Senior Paralegal- 6 month contract (78580)

      Senior ParalegalLocation:  Downey, CA  90242Duration:  6-month assignment (W2)Job Number:  78580 Job Description:Provide paralegal support to the Corporate and Commercial Law practice group, the Department’s external and internal clients, and outside counsel Top Daily Responsibilities:·         Manage intake of and response to regulatory affairs issues / inquiries, including: maintaining ...

    4. Regularly Affairs Specialist - Medical Device

      Hello, My name is Domenic and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Sr. Regulatory Affairs Specialist – Medical Device for a prominent client of ours.  This position is located in Diamond Bar, CA/Irvine, CA. Details for the position are as follows: Job Description:SUMMARY OF THE JOBDevelop regulatory submissions and assessments (in ...

    5. Regulatory Affairs Specialist

      Quest is seeking a Regulatory Affairs Specialist who will be responsible for successfully implementing and scaling the company’s global regulatory and compliance program to support bringing our products to the market globally. The role will ensure that Quest is in compliance with all applicable domestic and international laws, regulations and customs for key markets at both the ingredient and ...

    6. Document Control Technician

       The Document Control Technician is responsible for processing and maintaining all controlled documents in regulatory affairs. Responsibilities include creating, editing, indexing, tracking, and storage of documents as cGMP guidelines.Responsibilities: Issuance of approved SOP’s and maintain a log of all SOP’s on the floor.File and maintain SOP's, Master and executed batch records, packaging, ...

    7. Regulatory Affairs Associate

      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 AssociateJob ID: 2391Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 18-Month ContractPay Rate Range: Depends on Experience (W2, no ...

    8. Reporter, Los Angeles

      Law360, a LexisNexis company, is an online newswire for business lawyers that covers major litigation, transactions and regulatory issues. Founded in 2004 and acquired by LexisNexis in 2012, Law360 is a cutting-edge organization and one of the fastest-growing subscription news services in the U.S. Our subscribers include the 100 largest law firms in the U.S., in-house counsel at major ...

    9. Associate Director, Clinical Trials Office

      The Associate Director will be responsible for quality assurance, clinical operations, strategic planning, finance, project management, and regulatory compliance at Clinical Trials Office (CTO). The Associate Director will work with all relevant internal and external functional areas to execute clinical trials, including timelines, milestones and resources, for CTO. The Associate Director ...

    10. Director Regulatory Affairs

      Overview: As part of the leadership team the Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies for Class II/III medical devices This individual will be the Regulatory subject matter expert for all applicable medical devices. S/he will need to identify, assess and communicate regulatory development and submission strategies, ...

      1. Medical Science Liaison, Sleep (Midwest or Southeast) at Jazz Pharmaceuticals

        Thorough understanding of applicable federal and state regulatory requirements for field-based scientific personnel....

      2. Senior Medical Science Liaison, Sleep (Ohio Valley) at Jazz Pharmaceuticals

        Thorough understanding of applicable federal and state regulatory requirements for field-based scientific personnel....

      3. Vice President of Integrated Delivery System Strategy at Cigna

        Coordinate with the compliance team members responsible for interacting with Cigna Legal and Governmental affairs....

      4. STATISTICIAN - CANCER CENTER WHELAN RESEARCH - MSW at Mount Sinai Health System

        Regulatory affairs of the IRB. Meets regulatory, licensure and annual health. Mount Sinai Health System Careers....

      5. IT Lead, Regulatory Affairs Business Analyst R&D at Johnson & Johnson Medical NV

        We are looking for an IT leader that, with oversight from the IT Regulatory Affairs Product Line Organization, will partner with the R&D Regulatory Affairs...