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 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 Fri 18th April

  • 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 2 days ago

  • 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

  • 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 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

  • 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

West North Platte Job Search Tip

Customer service is a requirement of every company and business that expects to be successful. Representatives are hired who can handle customer relations, issues and questions. The job outlook for this type of work is very good because of its relevance to any successful business. Plus, minimal education is required to get started in a customer service position. On-the-job experience can be as important as education in receiving promotions within a company. As young customer service representatives are promoted or move into other positions, the turnover rate is high for this type of work, allowing for many available opportunities. Often there are many more jobs available than there are job seekers to fill them.

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