Regulatory Affairs Specialist Jobs

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  • Regulatory Affairs Specialist(Orange County, California)

    Medical Device Development, Manufacturing, and Distribution Company located in Carlsbad, California has an immediate opportunity available for a Regulatory Affairs Specialist. The Regulatory Affairs Specialist will be responsible for U.S. and International regulatory submissions for new product approvals - (510ks, IDEs, PMAs, Design Dossiers, and Canadian Medical Device Submissions) as well as mai...
    Full job description at Monster

    Posted Wed 12th March

  • Offshore GOM Regulatory Affairs Specialist - Oil & Gas Operating Co.Piper-Morgan Associates(Houston, Texas)

    Exceptional opportunity for the talented Regulatory Affairs Specialist with this progressive, independent oil and gas operating company with substantial offshore production. Please read carefully the following job description. Qualificed candidates are invited to email a detailed, chronological resume in MS Word format as an attachment and please include all dates for education and experience to: ...
    Full job description at Monster

    Posted Thu 13th March

  • Sr. Regulatory Affairs Specialist - North AmericaBerlin Heart Inc.(Houston, Texas)

    POSITION PURPOSE The Sr. Regulatory Affairs Specialist will be responsible for organizing, submitting and managing the regulatory activities. The Sr. Regulatory Affairs Specialist will also provide oversight for safety review including the reporting of MDR or product reports to FDA and Health Canada. The successful candidate will be responsible for management and oversight of the company’s submiss...
    Full job description at Monster

    Posted Tue 25th March

  • Regulatory Affairs SpecialistJoule Clinical(Northern, New Jersey)

    Title: Regulatory Affairs Specialist Location: Mahwah NJ, 07430 Positions: 3 (PLEASE REFER!) Requirements: § BA/BS. Engineering strongly preferred § RAC certification desired § Minimum 1+ years’ experience in FDA regulated industry § Working knowledge of Medical Device Regulations (FDA required) Core Responsibilities: § Plan, organize and implement strategies and activities required to procure reg...
    Full job description at Monster

    Posted Fri 28th March

  • Regulatory Affairs Specialist (1 To 3 Years Of Medical Device Exp)Qtech Solutions Inc.(Central, New Jersey)

    REG AFFAIRS SPECIALIST: RARITAN, NJ 6-24 months The Regulatory Affairs Specialist will be responsible for managing and overseeing the coordination, compilation and submission of regulatory applications to worldwide regulatory agencies, including new licenses/registrations, and will support day to day Regulatory Operations. The ideal candidate will interpret regulatory requirements and develop stra...
    Full job description at Monster

    Posted Wed 2nd April

  • Regulatory Affairs Specialist - Medical DeviceAgile Search Inc(Framingham/Worcester, Massachusetts)

    As a Regulatory Specialist with this medical device company, you will develop and implement regulatory strategies and submissions, support effective dialogue with U.S. and International regulatory authorities, prepare U.S. and International regulatory submissions, and facilitate timely product registrations and regulatory approvals. The Regulatory Affairs Specialist II will support corporate regul...
    Full job description at Monster

    Posted Thu 3rd April

  • Regulatory Affairs SpecialistInogen(Dallas, Texas)

    About Inogen Inogen was founded in 2001 to improve quality of life and increase freedom and independence for oxygen therapy users. Inogen is innovation in oxygen therapy. The Inogen mission is to improve freedom and independence for oxygen therapy patients through innovative products and services. Inogen is a manufacturer and Accredited Homecare Provider. Inogen is a growing company that is focuse...
    Full job description at Monster

    Posted Thu 3rd April

  • Regulatory Affairs SpecialistFladger Associates(Central, New Jersey)

    Responsibilities: Excellent employment opportunity for a Regulatory Affairs Specialist in Raritan, NJ area. Manage and oversee the coordination, compilation and submission of regulatory applications to worldwide regulatory agencies, including new licenses/registrations, and will support day to day Regulatory Operations. The ideal candidate will interpret regulatory requirements and develop strateg...
    Full job description at Monster

    Posted Thu 3rd April

  • Regulatory Affairs SpecialistMedSource(Raleigh/Durham-RTP, North Carolina)

    -SUMMARY: • The Regulatory Affairs Specialist supports the Company’s regulatory function and project teams through the provision of a variety of administrative and technical tasks involving the management of clinical research trials documentation. In addition, the Regulatory Affairs Specialist performs a variety of research, database, and administrative duties of a routine and technical nature in ...
    Full job description at Monster

    Posted Thu 3rd April

  • Regulatory Affairs Specialist - Medical DevicesGlobal Medical Devices Leader(Orange County, California)

    Regulatory Affairs Specialist - Medical Devices Global leader in the development of life saving medical devices seeks a regulatory affairs specialist to lead regulatory submittals to the FDA and other regulatory agencies. The Regulatory Affairs Specialist will: Write, coordinate, compile and submit regulatory documents to FDA, EPA, TUV and other international regulatory agencies. Prepare internati...
    Full job description at Monster

    Posted Tue 8th April

  • Medical Device Regulatory Affairs SpecialistSpartan Search Group(Northern, New Jersey)

    Spartan Search Group is the premier placement firm for technical positions both permanent and contract. With a primary focus on the Northeastern USA, we work with all Medical Device companies large and small and are in constant contact with the top tier, game-changing technical leaders in our industry. We are currently working with a major New Jersey-based Medical Device company that has an immedi...
    Full job description at Monster

    Posted Wed 9th April

  • Regulatory Affairs SpecialistSolomon Page Group(Columbus/Zanesville, Ohio)

    Regulatory Affairs Specialist Location: Columbus Contract: 3+ months Shift: 1st Salary: Based on Experience We are currently seeking a regulatory affairs professional to work a contract assignment for my client in Columbus, Ohio. Below is a list of the qualifications. · Manage the document process for regulatory submissions to the FDA · Experience in the pharmaceutical, food or cosmetic industry a...
    Full job description at Monster

    Posted Fri 11th April

  • Sr. Regulatory Affairs Specialist (Sylmar Or Sunnyvale)St. Jude Medical, Inc.(Los Angeles, California)

    At St. Jude Medical every one of us plays a role in our collective ability to save and improve lives. As an organization, we want to continue to grow and lead our industry in changing the way the world views the treatment of expensive, epidemic diseases. By seeing things from a different perspective, using our imagination, leading with character, and working with passion, we all have a role to pla...
    Full job description at Monster

    Posted Fri 11th April

  • Regulatory Affairs SpecialistUS Tech Solutions(South Bend, Indiana)

    Regulatory Affairs Specialist Warsaw, IN Duration: 12 Months Job Description: · Responsible for assisting the team with regulatory filings as necessary to market client products. This is an experienced level position, providing training towards full competency in Regulatory Affairs (RA). This position requires an intermediate understanding of client products and their use as well as an understandi...
    Full job description at Monster

    Posted Fri 11th April

  • Regulatory Affairs And Product Certification SpecialistPCB Piezotronics, Inc.(Buffalo, New York)

    REGULATORY AFFAIRS AND PRODUCT CERTIFICATION SPECIALIST Work with regulatory agencies to understand upcoming changes and determine the impact to new and legacy products. Enforce regulatory and safety standards during new product development. Develop processes to ensure that legacy product remains compliant. Responsible for guarantying existing products are up to date. Review Country/Region specifi...
    Full job description at Monster

    Posted Sat 12th April

  • Sr Specialist QA/Scientific/Regulatory AffairsJudge Group(, California)

    Our client seeks a Sr Specialist QA/Scientific-Regulatory Affairs for a permanent opportunity. Great benefits!!! Successful candidate ensures compliance to FDA and other applicable regulations. Prepares, analyzes, and submits dossiers to various governing agencies in supporting business growths. Supports applicable regulations including ISO, local, state, and/or federal requirements. • Monitor pro...
    Full job description at Monster

    Posted Mon 14th April

  • Sr. Regulatory Affairs SpecialistBioness(Los Angeles, California)

    Bioness (www.bioness.com) offers award-winning medical devices designed to benefit people with Stroke, Multiple Sclerosis, Traumatic Brain Injury, Cerebral Palsy and Spinal Cord Injury. These products use Functional Electrical Stimulation (FES) to help people regain mobility and independence to improve quality of life and productivity We are searching for an enthusiastic and self-motivated Sr. Reg...
    Full job description at Monster

    Posted Mon 14th April

  • Senior Regulatory Affairs Specialist Or ManagerSystem One(Northern, New Jersey)

    Rising pharmaceutical company is seeking a Senior Regulatory Affairs Specialist or Manager level to join their team. The company has a robust clinical pipeline including an upcoming phase III study. This will be an individual contributor role instrumental in all aspects of Regulatory Affairs. This is a tremendous opportunity to work with a collaborative group of scientists and professionals commit...
    Full job description at Monster

    Posted Wed 26th March

  • Global Regulatory Affairs Integration Activities SpecialistKaztronix LLC(Oakland/East Bay, California)

    Job Title: Global Regulatory Affairs Integration Activities Specialist Location: Emeryville, CA Duties: This position will be responsible for supporting the integration activities from Client Diagnostics. Scope of work would include compiling of rest of world submissions, ordering required certificates, and tracking of submission under Health Authority review. The position would also be responsebl...
    Full job description at Monster

    Posted Wed 16th April

  • Regulatory Affairs And Product Certification SpecialistPCB Piezotronics, Inc.(Buffalo, New York)

    Regulatory Affairs and Product Certification Specialist PCB Piezotronics, Inc. is a global leader in the manufacture of piezoelectric and strain gauge sensors.The success of PCB is in our people. It is our philosophy to hire good people and support them in doing their job. PCB’s Management is committed to providing asupportive and challenging work environment. The Company’s professional working co...
    Full job description at Monster

    Posted Thu 17th April

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