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regulatory affairs in Los Angeles

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  1. Director, CMC Regulatory Affairs at Kite Pharma, Inc.

    Preparation for regulatory agency meetings, regulatory review and approval of cGMP documentation, and general regulatory compliance activities....

  2. Sr. Regulatory Affairs Specialist at Second Sight, Inc.

    Regulatory Affairs Specialist*. Regulatory Affairs Certification (RAC) or equivalent required. Regulatory Compliance PMA 510K:....

  3. Vice President Regulatory CMC at Dennis Partners

    Minimum 12-15 years regulatory affairs experience Minimum of a Masters in a scientific discipline required, Ph.D....

  4. Coordinator III-Regulatory at L'Oreal USA

    The Regulatory Affairs Coordinator is responsible to support, and maintain procedures in the Regulatory Affairs Department to ensure the compliance of all...

  5. Labor Engagement Coordinator Public Sector - Rockville, MD at Kaiser Permanente

    Responsible for the creation, compilation, and submission/filing of all required legal, financial, and regulatory documentation, including the development and...

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    1. US Regulatory Affairs Professional

      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: US Regulatory ProfessionalJob ID: 2359Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 18 Month ContractPay Rate Range: Depends on Experience (W2, no ...

    1. Program Director, Human Services, College Degree & 3 Yrs Exp Req at Dungarvin

      Ensure compliance with regulatory requirements. Monitor financial affairs of persons served. The Administrator must meet the regulatory requirements of...

    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. 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. Clinical Research Associate

      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 ...

    1. Chair, Department of Clinical Research & Leadership at George Washington University

      The chair will be responsible for: ensuring the overall quality of the department’s online and blended academic programs; effective management of departmental

    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. Program Coordinator at Loyola Marymount University

      Collaborate with the Divisional Student Affairs Research and Assessment Office. Keep apprised of changing federal regulations and disseminate regulatory...

    1. Sr. Regulatory Affairs Specialist

      Currently looking for an experienced Sr. Regulatory Affairs Specialist to fill an opening with Second Sight (www.2-sight.com) located in Sylmar, CA. The ideal candidate will hold a Bachelor’s degree in Engineering, Physical or Biological Sciences and the Regulatory Affairs certification (RAC) or equivalent qualification.Responsibilities of the Sr. Regulatory Affairs Specialist·         ...

    1. VP of Clinical Program Development at Fairway Consulting Group

      Broad knowledge of Drug Development and on market Medical Affairs. Key contributor to medical and scientific documents for clinical trials as well as documents...

    1. Program Director (Administrator)

      Dungarvin…Respecting and responding to the choices of people in need of supportsDungarvin is seeking to fill a position in the following capacity:Program Director (Administrator)To support the continuous enrichment of individuals with developmental disabilities in ourADULT RESIDENTIAL FACILITIES FOR PERSONS WITH SPECIAL HEALTH CARE NEEDS Westchester (Los Angeles, CA)We believe each person has ...

    1. Sr Safety Specialist (United States) at INC Research

      (GCPs), regulatory guidelines, and study procedures. Evaluates AE data for completeness, accuracy and regulatory reportability....

    1. Clinical Research Associate

      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 accurate and timely completion of studies, including project ...

    1. Biostats Specialist at Career Developers

      Actively provide statistical support to the Medical Affairs Department. Work under the direction of Medical Affairs Statistics Disease Lead the Contract...

    1. Clinical Affairs - Administrative Assistant

      POSITION SUMMARY:  Assists with the preparation and maintenance of clinical studies and submissions and other documents to conduct clinical trials with end goal of receiving product clearance / approvals in conformance with U.S. FDA, CSA, and CE Mark and other regulatory and notified bodies’ requirements. SPECIFIC DUTIES AND RESPONSIBILITIES:Responsible for creating an excel spreadsheet for ...

    1. Compliance Specialist at Wright Medical Technology, Inc.

      Bachelor’s Degree, preferably in business or legal areas or relevant experience3-5 years of experience in Compliance, Medical Education, Contracting, Marketing...

    1. Sr. Regulatory Affairs Associate

      TOP SKILLS: 1-2 years of experience in regulatory affairs, or biotech industry Basic Qualifications * Bachelor’s degree and 2 years Regulatory or Regulatory CMC experience OR * Associate’s degree and 6 years Regulatory or Regulatory CMC experience OR * High school diploma / GED and 8 years Regulatory or Regulatory CMC experience Preferred Qualifications * Document management system experience ...

    1. Regulatory Affairs Specialist at Validant

      Regulatory Affairs Specialists – Primary responsibilities include:. Validant is seeking Regulatory Affairs professionals with medical device experience for...

    1. Reprocessing Specialist

      This position manages and provides support for the activities of the reprocessing qualification/validation for all KARL STORZ (KS) products, including cleaning, disinfection and sterilization studies with existing and upcoming chemicals and equipment for reprocessing. This position coordinates activities with KS global counterparts to support product cleaning, high level disinfection and ...

    1. Regulatory Affairs Specialist at ACell

      Regulatory Affairs Specialist. The Regulatory Affairs Specialist assists the Head of Regulatory Affairs with US and international activities relating to...

    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 ...

    2. Senior Associate

      Title: Senior Associate Regulatory AffairsLocation: Thousand Oaks, CAType: Contract position ( 7 months, possible extension), $ 33.00 - 37.00 an hourly ratePerson must be onsite in Thousand Oaks, CAResponsible for support and maintenance of State Wholesale Licensing Program, as well as other CMC Team functions.The team needs assistance with numerous and varying state license renewals, ...

    3. Manager of Quality

      This position performs complex and varied managerial work developing, planning and coordinating quality improvement activities by ensuring that corporate level quality directives and projects are accomplished. Work requires the direct application of a variety of procedures, policies and/or precedents.Essential Functions (Major Duties and Responsibilities):Assist Director with the ...

    4. 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 ...

    5. Research Lab Manager

      Required Skills & Qualifications:•  BS degree in Biochemistry or a related degree required. MS / PhD highly desired.•  LC-MS/MS proficiency and experience with immunoassay and related laboratory methodologies •  Experience with, and knowledge of, managing and supervising the daily operation of a licensed clinical                 research laboratory in accordance with Good Laboratory Practices ...

    6. 99980 – Sr. Associate Regulatory Affairs

      Job Description:The Regulatory Professional under the direction of a Regional Regulatory Lead will assist in the creation and submission of regulatory documents and may be the regulatory lead for a program under the supervision of a more experienced regulatory lead.Key Activities:• Assist Regional Regulatory Lead to support regional regulatory activities (e.g. IMPD development and submission, ...

    7. Field Based Medical Director

      Field Based Medical Director – Dementia/Diagnostic imaging, California, USA. Medical Affairs Roles, and key responsibility:Provide scientific support for medical affairs and commercial activities, explore investigational research opportunities, and report safety issues consistent with legal and regulatory requirements.Primary function: to identify and engage national, regional and local ...

    8. Field Based Medical Director

      Job title:  Field Based Medical Director - Dementia/Diagnostic imaging, California, USA. Medical Affairs  Roles, and key responsibility: Provide scientific support for medical affairs and commercial activities, explore investigational research opportunities, and report safety issues consistent with legal and regulatory requirements. Primary function: to identify and engage national, ...

    9. Law360: 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 ...

    10. Manager, Reprocessing and Sterilization

      Job Summary: KARL STORZ as a device manufacturer is regulated by the FDA in the United States, and similar authorities in other countries. In order to market and sell KS products, we must comply with any applicable regulations in each country in which the products are sold. The primary areas of compliance include United States' Federal Code of Regulations for medical devices and Health ...

      1. Wheat Trait Development Coordinator and Sabin Site Manager at BAYER

        Accountable for adherence to local regulations and Regulatory Affairs and Stewardship Directives, QHSE, and responsible for site budget spending;...

      2. REGULATORY AFFAIRS COORDINATOR at Greenville Health System

        2 years- Clinical research, regulatory affairs, and/ or experience in an oncology related field. Coordinates the research and administrative activities of...

      3. Regulatory Affairs Coordinator at 3M

        At least 5 years in Regulatory Affairs and Documentation Activities for Medical Devices. 3M está buscando un Regulatory Affairs Coordinator para el Negocio de...

      4. Associate Director of Clinical Affairs at Cure SMA

        Experience with clinical drug development process and regulatory issues required. The Associate Director of Clinical Affairs will oversee the day-to-day...

      5. Psychiatric Technician, Become a Program Director (Human Services) at Dungarvin

        Ensure compliance with regulatory requirements. Monitor financial affairs of persons served. The Administrator must meet the regulatory requirements of...