Regulatory Affairs Associate Jobs

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  • Regulatory Affairs Associate 2Onyx Pharmaceuticals(San Francisco, California)

    Apply Directly Here - http://jobvite.com/m?3SjUJfwy Primary Duties Assist with the coordination, review and preparation of clinical trial applications, ensuring compliance with the Food and Drug Administration (FDA) and international regulations and interpretations Represent Regulatory Affairs on Study Execution Teams (SET) for the clinical development and clinical trials (phase 2 and 3) of invest...
    Full job description at Monster

    Posted Thu 7th March

  • Associate, Regulatory AffairsHospira(Chicago North, Illinois)

    Summary : The Regulatory Affairs Associate assists in the definition of global regulatory requirements and review of data submitted by project team members. Assembles and prepares regulatory submissions and other regulatory documents to regulatory agencies. Major Duties and Responsibilities: With oversight, collaborates with other functional areas to obtain documentation for regulatory purposes. S...
    Full job description at Monster

    Posted Mon 11th March

  • Associate Director, Regulatory Affairs, BiologicsHospira, Inc.(Chicago North, Illinois)

    The Associate Director, Regulatory Affairs, Biologics will support the timely and effective registration of Hospira's biologics product portfolio by overseeing and contributing to the process by which new products are developed in line with the global registration requirements of targeted countries and by obtaining expedient registration of these products in a cost effective manner. Maintains regi...
    Full job description at Monster

    Posted Mon 11th March

  • Regulatory Affairs AssociateAbbott(Chicago, Illinois)

    Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 70,000 people. The Regulatory Affair...
    Full job description at Monster

    Posted Mon 11th March

  • Sr. Regulatory Affairs Associate – International (Med Device A Must)Thoratec Corporation(Oakland/East Bay, California)

    Pioneering Therapies, Transforming Lives.What does it mean to be part of the Thoratec Team? It means working in a fast-paced environment that inspires you. It means collaborating on projects that literally save patients' lives. We have an incredible opportunity for a Sr. Regulatory Affairs Associate - International to work with our innovative Regulatory team in Pleasanton, CA. The Sr. Regulatory A...
    Full job description at Monster

    Posted Wed 13th March

  • Associate Director CMC Regulatory AffairsShire(Boston, Massachusetts)

    Primary Duties: The Associate Director of CMC Regulatory Affairs will serve as the global product leader for CMC regulatory strategy of one or more biological and/or small molecule products. This will include formulating and implementing CMC regulatory strategies for the development of protein therapies, lead CMC regulatory activities for assigned projects in line with US or ICH requirements. Prim...
    Full job description at Monster

    Posted Thu 14th March

  • Sr. Associate-Specialist, Regulatory Affairs-Operations JobNovo Nordisk Inc.(Central, New Jersey)

    Requisition ID 11974BR Title Sr. Associate/Specialist, Regulatory Affairs-Operations Job Category Regulatory Affairs Job Description PURPOSE: The Regulatory Operations Senior Associate/Specialist will support the global extent of e-submissions and use of Insight Publisher and/or Novodocs for regulatory submissions in Novo Nordisk and will identify, analyze and develop technical solutions that impr...
    Full job description at Monster

    Posted Fri 15th March

  • ASSOCIATE DIRECTOR, REGULATORY AFFAIRS - CMC JobJohnson & Johnson(Central, New Jersey)

    Johnson & Johnson companies are equal opportunity employers. ASSOCIATE DIRECTOR, REGULATORY AFFAIRS - CMC-8916120703 Description Janssen Research & Development, L.L.C., a member of Johnson & Johnson&'s Family of Companies, is recruiting for an Associate Director, Regulatory Affairs - CMC, located in Raritan or Titusville, NJ OR Spring House, PA OR Fremont, CA OR Beerse, Belgium. Janssen Research &...
    Full job description at Monster

    Posted Wed 27th February

  • Regulatory Affairs AssociateMedivators(Minneapolis, Minnesota)

    JOB PURPOSE: The Regulatory Affairs Associate supports and improves Medivators regulatory compliance position by completing regulatory compliance related tasks to help achieve RA departmental objectives. Coordinate the handling, follow-up and closure of product complaints including completion of adverse event reports when necessary. Maintain complaint handling process documentation and regulatory ...
    Full job description at Monster

    Posted Mon 25th March

  • Regulatory Affairs Associate IIINovartis(Eastern/Greenville, North Carolina)

    Regulatory Affairs Associate III Business Unit: Sandoz - United States Division: Sandoz Company/Legal Entity: Sandoz, Inc Job Reference Code: 115166BR The Regulatory Affairs Systems Associate III is responsible for the review of regulatory affairs submissions and implementation of regulatory systems including maintenance of electronic regulatory documentation. This position interacts broadly with ...
    Full job description at Monster

    Posted Mon 25th March

  • Regulatory Affairs AssociateRandstad Pharma(Ventura County, California)

    Job Title: Regulatory Affairs Associate Position Description Under general supervision, this position is responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical and scientific data and reports required for submission in support of company’s products. Position Responsibilities Experience with review and formatting of regul...
    Full job description at Monster

    Posted Wed 27th March

  • Regulatory Affairs Associate - Horsham, PAUnitedHealth Group(Philadelphia, Pennsylvania)

    Description: The Regulatory Affairs Associate will review enacted state/federal laws and regulations for impact to Insurance Solutions products/services and prepare Legislative Bulletin reports describing the impact of these requirements. This individual will work with department managers and business leaders to ensure understanding and compliance with changes in state/federal requirements. This p...
    Full job description at Monster

    Posted Mon 25th March

  • Sr. Regulatory Affairs Associate – (Med Device A Must)Thoratec Corporation(Boston North, Massachusetts)

    Pioneering Therapies, Transforming Lives.What does it mean to be part of the Thoratec Team? It means working in a fast-paced environment that inspires you. It means collaborating on projects that literally save patients' lives. We have an incredible opportunity for a Sr. Regulatory Affairs Associate to work with our innovative Regulatory team in Burlington, Massachusetts. The Sr. Regulatory Affair...
    Full job description at Monster

    Posted Mon 1st April

  • Regulatory Affairs AssociateLannett Co., Inc.(Philadelphia, Pennsylvania)

    Awarded the Deloitte Touche Technology Fast 500 Award as one of the fastest growing companies in North America in 2010, Lannett is the fast-forward leader in the manufacture of generic pharmaceuticals as well as being a one-stop, blend to bottle manufacturer. Lannett Company, Inc. is seeking a highly talented and self- motivated professional to join our team as a Regulatory Affairs Associate in ou...
    Full job description at Monster

    Posted Tue 2nd April

  • Associate Project Manager, Regulatory Affairs (2011237)Perrigo Company(Minneapolis, Minnesota)

    Perrigo is the world's largest manufacturer of over-the-counter pharmaceutical and nutritional products for the store brand and contract manufacturing markets and an emerging developer, manufacturer and marketer of prescription generic drugs. An exciting career opportunity is currently available on the Regulatory Affairs (RA) team at Perrigo’s facilities located just outside of Minneapolis, Minnes...
    Full job description at Monster

    Posted 3 days ago

  • Associate Director Regulatory AffairsDennis Partners(Boston, Massachusetts)

    Associate Director Regulatory Affairs Are you looking for the kind of opportunity where your ideas will influence the direction of your department as it moves into the future? My client, a Boston based biotechnology company is seeking a qualified Associate Director Regulatory Affairs to join their promising team! This regulatory group has a work-hard/play-hard sensibility with a never-let-them-see...
    Full job description at Monster

    Posted Fri 8th February

  • Regulatory Affairs AssociateTeva Pharmaceuticals(Northern, New Jersey)

    Overview: Come and join Teva on its journey of growth. Teva has been cultivating excellence for over a century, and is today a worldwide leading generic pharmaceutical company and one of the top 15 companies in the industry. With 46,000 employees in 60 countries worldwide, we are proud to say that our employees are the reason for our sustained success. Their skills and dedication make us an indust...
    Full job description at Monster

    Posted Wed 27th March

  • Regulatory Affairs AssociateTeva Pharmaceuticals(Philadelphia, Pennsylvania)

    Overview: Come and join Teva on its journey of growth. Teva has been cultivating excellence for over a century, and is today a worldwide leading generic pharmaceutical company and one of the top 15 companies in the industry. With 46,000 employees in 60 countries worldwide, we are proud to say that our employees are the reason for our sustained success. Their skills and dedication make us an indust...
    Full job description at Monster

    Posted Wed 27th March

  • Regulatory Affairs AssociateTeva Pharmaceuticals(Philadelphia, Pennsylvania)

    Overview: Come and join Teva on its journey of growth. Teva has been cultivating excellence for over a century, and is today a worldwide leading generic pharmaceutical company and one of the top 15 companies in the industry. With 46,000 employees in 60 countries worldwide, we are proud to say that our employees are the reason for our sustained success. Their skills and dedication make us an indust...
    Full job description at Monster

    Posted Wed 27th March

  • Regulatory Affairs AssociateTeva Pharmaceuticals(Northern, New Jersey)

    Overview: Teva Pharmaceuticals USA is the leading generic pharmaceutical company, marketing products from a wide range of therapeutic areas including analgesic, anti-infective, cardiovascular, oncology, CNS, dermatological and anti-inflammatory. Teva USA products are marketed to chains, wholesalers, distributors, hospitals, managed care entities, and government agencies. The company's mission is t...
    Full job description at Monster

    Posted Wed 27th March

Regulatory Affairs Associate Job Search Tip

The industry is stabilized by the factory workers who actually produce and the industrial production managers who oversee the work. For the production jobs that are available, they can be very lucrative positions that pay well. They are also physically demanding, noisy jobs that require shift work and overtime to meet production deadlines. Managers often work regular 40-hour weeks, but are on call to come in to resolve problems no matter what time they occur.

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