Regulatory Affairs Associate Marketing Jobs

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  • Regulatory Affairs Associate - Medical DevicesMRINetwork(San Diego, California)

    Regulatory Affairs Associate Medical Devices There is an immediate need for a Regulatory Affairs Associate with experience in medical devices in the Encinitas, CA area. This is an opportunity to join a fast growing company in the class I and class II business. They need someone that understands regulatory reporting, has knowledge of the 510k process and audits. A relocation package is available al...
    Full job description at Monster

    Posted Tue 23rd April

  • Regulatory Affairs Associate(Charlotte, North Carolina)

    Under general supervision of the Director of Regulatory Affairs, the RA Associate will perform drug listings per CFR requirements and calendar, and will review customer labeling for compliance to applicable CFR requirements for assigned pharmaceutical product categories. Research applicable regulations and scientific literature in product categories and work with the Director of RA and Account Man...
    Full job description at Monster

    Posted Tue 7th May

  • Regulatory Affairs AssociatePioneer Surgical(Northern, Michigan)

    Regulatory Affairs Associate This position provides training towards full competency in Regulatory Affairs (RA). Candidates may enter with no prior experience in RA, or may have up to two years + prior RA experience with IDE/PMA exposure. The selected candidate will develop expertise in areas that may include preparation of dossiers for product registrations outside the U.S.; preparation of submis...
    Full job description at Monster

    Posted Fri 17th May

  • Regulatory Affairs And Design Assurance AssociateMeridian Bioscience(Cincinnati, Ohio)

    Meridian is a fully integrated life sciences company that manufactures, markets and distributes a broad range of innovative diagnostic test kits, purified reagents and related products and offers biopharmaceutical enabling technologies. Utilizing a variety of methods, these products provide accuracy, simplicity and speed in the early diagnosis and treatment of common medical conditions, such as ga...
    Full job description at Monster

    Posted Fri 17th May

  • Regulatory Affairs Associate PrincipalGenzyme Corporation(Framingham/Worcester, Massachusetts)

    . Principal Associate, Regulatory Affairs, Site CMC The ideal candidate will have the mix of personal and professional characteristics with emphasis on the following job responsibilities: Be the Regulatory CMC site lead at the Genzyme Northborough MA facility Provide regulatory CMC support for site manufacturing operations (Packaging, Labeling, Warehousing, and Testing). Review technical documenta...
    Full job description at Monster

    Posted Yesterday

  • Regulatory Affairs, Associate Principal - Site CMCGenzyme Corporation(Boston, Massachusetts)

    . Regulatory Affairs, Associate Principal - Site CMC The ideal candidate will have the mix of personal and professional characteristics with emphasis on the following job responsibilities: Provide regulatory support for manufacturing operations at the Allston Landing Biologics Facility. Review technical documentation (Project Plans, Change Control, Deviations, CAPA, Batch Records) Recommends/appro...
    Full job description at Monster

    Posted Yesterday

  • Regulatory Affairs, Associate Principal - Site CMCGenzyme Corporation(Boston, Massachusetts)

    . Regulatory Affairs, Associate Principal - Site CMC The ideal candidate will have the mix of personal and professional characteristics with emphasis on the following job responsibilities: Provide regulatory support for manufacturing operations at the Allston Landing Biologics Facility. Review technical documentation (Project Plans, Change Control, Deviations, CAPA, Batch Records) Recommends/appro...
    Full job description at Monster

    Posted Yesterday

  • Regulatory Affairs Associate PrincipalGenzyme Corporation(Boston, Massachusetts)

    . We have an excellent opportunity in the Global RA CMC group supporting manufacturing site activities and the products manufactured therein in support of our medical devices. The position is based in Cambridge, MA. The ideal candidate will have the mix of personal and professional characteristics with emphasis on the following job responsibilities: Provide regulatory support for manufacturing ope...
    Full job description at Monster

    Posted Yesterday

  • Regulatory Affairs Specialist - Medical DevicesMRINetwork(San Diego, California)

    Regulatory Affairs Medical Devices There is an immediate need for a Regulatory Affairs Associate or Regulatory Affairs Specialist with experience in medical devices in the Encinitas, CA area. This is an opportunity to join a fast growing company in the class I and class II business. They need someone that understands regulatory reporting, has knowledge of the 510k process and audits either through...
    Full job description at Monster

    Posted Fri 10th May

  • Associate Medical Director (PhD, PharmD), Medical Affairs: Launch Of Cardio/Metabolic Drug, NJ PharmCornerstone Search Group, LLC(Northern, New Jersey)

    Associate Medical Director (PhD, PharmD), Medical Affairs: Launch of Cardio/Metabolic Drug, NJ Pharma Summary of Opportunity: Exciting opportunity to develop and manage the execution of the various Medical Affairs activities for the launch of a new drug to treat a very important condition. In this role, you will have the opportunity to handle a wide variety of Medical Affairs responsibilities whil...
    Full job description at Monster

    Posted Mon 29th April

  • Associate Director, Clinical Affairs / 3905B. Braun Medical Inc.(Allentown, Pennsylvania)

    Position Description: We are currently seeking an Associate Director of Clinical Affairs is responsible, in collaboration with the clinical Research Project Managers, for development and execution of the clinical research studies. The Associate Director will act in a supervisory capacity to the clinical Research Project Managers but will be jointly responsible for the delivery of timely trials wit...
    Full job description at Monster

    Posted Fri 10th May

  • Manager, Medical Affairs - Global Post-Marketing Commitments JobJohnson & Johnson(Philadelphia, Pennsylvania)

    Johnson & Johnson companies are equal opportunity employers. Manager, Medical Affairs - Global Post-Marketing Commitments-7757130507 Description Janssen Services, LLC , a member of the J&J family of companies is recruiting for a Manager, Medical Affairs - Global Post-Marketing Commitments, located in Horsham, PA. The Manager, Medical Affairs (MA) - Global Post-Marketing Commitments resides within ...
    Full job description at Monster

    Posted Fri 10th May

  • Associate Director, Regulatory Advertising And PromotionQuestcor(Oakland/East Bay, California)

    Overview: Questcor is a specialty biopharmaceutical company which was awarded Forbes’ Magazine’s #1 Best Small Company award in 2011 and Orange County Register’s #1 Best Large Company of 2012. We help patients with serious, difficult-to-treat autoimmune and inflammatory disorders. Currently, we are supporting research in a number of rare conditions, including in treatment-resistant patient populat...
    Full job description at Monster

    Posted Wed 8th May

  • Senior Regulatory AssociateMedimetriks Pharmaceuticals Inc.(Northern, New Jersey)

    Medimetriks Pharmaceuticals, Inc. is a specialty pharmaceutical company. Our Mission is to develop, license and commercialize innovative prescription skincare brands that fill unmet needs in the Dermatology and Podiatry markets. Who Are We Looking For? We are seeking a senior regulatory associate to support our Regulatory Department at our Headquarters in Fairfield, NJ. Requires excellent communic...
    Full job description at Monster

    Posted Fri 17th May

  • Senior Product Manager / Associate Director US Marketing - Specialty - Small Biopharma In CTParkwood International(New Haven, Connecticut)

    Senior Product Manager / Associate Director US Marketing - Nephrology My client, a small, global, publicly traded biopharmaceutical company, based in CT (2 hours from Boston and 1 ½ hours from NYC) develops drugs that inhibit certain immune system functions that cause auto immune disorders, cancers, and other diseases. Their marketed product is for the treatment of a rare genetic blood disorder. T...
    Full job description at Monster

    Posted Tue 9th April

  • Dean Of Student AffairsThe Art Institutes(San Antonio, Texas)

    Job Summary: This position is responsible for providing vision, leadership, initiative and strategic direction for student affairs and the overall campus community. Will ensure the delivery of effective and quality service to students in the following areas: student housing, student support and wellness, student conduct, effective co-curricular student programs, assessment, disability services, st...
    Full job description at Monster

    Posted Wed 8th May

  • Dean Of Student Affairs - Ai New York CityThe Art Institutes(New York City, New York)

    Job Summary: This position is responsible for providing vision, leadership, initiative and strategic direction for student affairs and the overall campus community. Will ensure the delivery of effective and quality service to students in the following areas: student housing, student support and wellness, student conduct, effective co-curricular student programs, assessment, disability services, st...
    Full job description at Monster

    Posted Fri 17th May

  • Statistician/SAS(remote),Data Manager,CRS,Medical Affairs,Clinical Manager,Informed Consent SpecialTechData(Northern, New Jersey)

    TechData is hiring Biostatistician (Some positions can be telecommute), SAS Programmer/Statistical Programmer (Some can be telecommuting), Sr. Clinical Data Manager, Director of Medical Affairs, Informed Consent Specialist, Clinical Scientist, CRS (Clinical Research Scientist), Clinical trial manager/Leader for our pharmaceutical clients in Northern and Central NJ. Please see below requirements an...
    Full job description at Monster

    Posted Yesterday

  • Senior Clinical Research AssociateInfobahn Softworld Inc(Minneapolis, Minnesota)

    Please send me your updated resume if you are comfortable for the below requirement. Job Title: Clinical Research Associate Primary Skills: BS, medical device, clinical research Location: Plymouth MN(locals) Duration: 12 months No. of Positions: 1 Position Type: Contract Job Description: This contract position was planned and budgeted for in the Drug Coated Balloon (DCB) proforma and is necessary ...
    Full job description at Monster

    Posted Thu 25th April

  • Associate Editor, Editorial ServicesForest Laboratories, Inc.(New York City, New York)

    Position Description This position works within the Editorial Services group to review planned promotional materials and programming initiatives, both print and electronic, for Forest brands. Position provides editorial support at all stages of the promotional review process and is responsible for research and reference checks regarding data and claims, grammatical and factual accuracy, for ensuri...
    Full job description at Monster

    Posted Tue 14th May

Regulatory Affairs Associate Job Search Tip

College graduates who have experience and creative ideas to market their employer's products or services will fare best in the marketing industry. They will face competition from other college graduates for the same advertising, marketing, promotion, or public relations positions. This growth of the marketing industry will be powered by the competition between companies to sell their products and services. High earnings, benefits and bonuses, travel and long hours including weekends are common. Median salaries of managers are very high in the marketing industry.

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