West North Platte Regulatory Affairs Specialist Jobs

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  • Senior Regulatory Affairs Specialist (1 Of 2) JobJohnson & Johnson Family Of Companies(Philadelphia, Pennsylvania)

    Johnson & Johnson companies are equal opportunity employers. Senior Regulatory Affairs Specialist (1 of 2)-4446140219 Description DePuy Synthes Companies of Johnson & Johnson is seeking a Senior Regulatory Affairs Specialist - CMF in West Chester, PA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world. D...
    Full job description at Monster

    Posted Thu 17th April

  • 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

  • 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 SpecialistThe Fountain Group(Philadelphia, Pennsylvania)

    We are a national staffing firm and are currently seeking a Regulatory Affairs Specialist for a prominent client of ours. This position is located in Wes Chester, PA. Details for the positions are as follows: Job Description: Minimum of 7 years’ experience in the medical device and/or pharmaceutical industries. Working knowledge of US FDA regulations. International or global scale experience is pr...
    Full job description at Monster

    Posted Thu 17th April

  • Regulatory Affairs SpecialistKaztronix LLC(Philadelphia, Pennsylvania)

    Pharmaceutical International is seeking an Analyst, Regulatory Compliance Support & Testing located in West Chester, PA Pharmaceutical, through its operating companies, is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. We strive to provid...
    Full job description at Monster

    Posted Wed 16th April

  • REGULATORY AFFAIRS SPECIALIST IV JobJohnson & Johnson Family Of Companies(Orange County, California)

    Johnson & Johnson companies are equal opportunity employers. REGULATORY AFFAIRS SPECIALIST IV-5680140305 Description Advanced Sterilization Products (ASP) a member of Johnson & Johnson Family of Companies, is recruiting for Regulatory Affairs Specialist, 4, in Irvine, CA. ASP (Advanced Sterilization Products), a member of the Johnson & Johnson Family of Companies, is a leading designer and develop...
    Full job description at Monster

    Posted Wed 16th April

  • Regulatory Affairs SpecialistApex Systems(Boston North, Massachusetts)

    Apex Systems, a division of On Assignment (NYSE:ASGN) is working on a Regulatory Affairs Associate Position in Chelmsford, MA. The position is a 3-6 month contract with a reputable client. If interested, please forward over a resume to mlavoie@apexsystemsinc.com . Below are more details on the position. Look forward to hearing from you! Preferred Requirments 1. 3-4 years regulatory experience, und...
    Full job description at Monster

    Posted 3 days ago

  • Regulatory Affairs Leadership Development Program - United States JobJohnson & Johnson Family Of Companies(Central, New Jersey)

    Johnson & Johnson companies are equal opportunity employers. Regulatory Affairs Leadership Development Program - United States-00000MCJ Description The Medical Devices and Diagnostics (MD&D) franchise of Johnson& Johnson is recruiting a Regulatory Affairs Specialist II to join the Regulatory Affairs Leadership Development Program (RALDP). This is a permanent, full-time position with J&J. Positions...
    Full job description at Monster

    Posted Today

  • Regulatory Affairs Specialist(San Diego, 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

  • 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-Diagnostic ProductsHologic, Inc.(San Diego, California)

    Hologic, Inc. (NASDAQ: HOLX) is a leading developer, manufacturer and supplier of premium diagnostics, medical imaging systems, and surgical products dedicated to serving the healthcare needs of women throughout the world. We are seeking a Regulatory Affairs Specialist II/III at our San Diego, CA office who will define, manage and execute complex, global regulatory submission strategies to help me...
    Full job description at Monster

    Posted Wed 2nd April

  • 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 SpecialistApplied Medical(Orange County, California)

    Applied Medical, a progressive medical device developer, manufacturer, and distributor, invites exceptional individuals to pursue careers in our innovative organization. If you would like to be a part of one of the fastest growing and most innovative companies in the medical device field, then Applied Medical is the place for you. Applied’s team members enjoy an environment that allows opportunity...
    Full job description at Monster

    Posted Tue 8th 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

  • Sr. Regulatory Affairs SpecialistProNova Sollutions, LLC(Knoxville, Tennessee)

    ProNova Solutions, LLC is aggressively developing the next generation of cancer therapy technology in a highly integrated proton therapy medical device. The fusion of state-of-the-art imaging, superconducting magnet technology, and unprecedented closed loop treatment verification using Positron Emission Tomography sets the ProNova product apart from all others. We are recruiting critical leadershi...
    Full job description at Monster

    Posted Wed 9th April

West North Platte Job Search Tip

In fall and winter hiring for seasonal jobs starts to pick up because companies are looking to get ready for the busy holiday season. Typically these companies are looking for people with previous experience who can quickly adjust to a work environment. Seasonal jobs are a great way to make extra money and also can be great for college and high school students who have a winter break.

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