West North Platte Regulatory Affairs Specialist Jobs

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  • Senior Regulatory Affairs SpecialistMichael Page USA(Chicago North, Illinois)

    About the company Our client is a manufacturer of class I & II medical devices and medical supplies that were founded over 100 years ago. With Chicago-based roots and a global footprint, their products can be found in almost 100 countries. Job description Seeking a high caliber Senior Regulatory Affairs Specialist. Act as a Regulatory Affairs representative during audits an support CAPA resolution...
    Full job description at Monster

    Posted Tue 5th August

  • Regulatory Affairs Specialist(Chicago North, Illinois)

    WORLD LEADING ORGANIZATION IN SEARCH OF AN EXPERIENCED REGULATORY AFFAIRS SPECIALIST FOR A ROLE IN CORPORATE HEADQUARTERS. REGULATORY AFFAIRS SPECIALIST RESPONSIBILITIES: 1. Responsible for new product registration and maintenance of existing registrations. 2. Review/approve production documentation. 3. Prepare and review clinical trial protocols and review final reports. 4. Review product labelin...
    Full job description at Monster

    Posted Tue 19th August

  • Regulatory Affairs Labeling SpecialistAkorn, Inc.(Chicago North, Illinois)

    Our Company We are a rapidly growing pharmaceutical manufacturer with strong lines in hospital and ophthalmic markets, and many new products in development and awaiting FDA approval. In anticipation of long-term, substantial growth, we offer challenging, attractive career opportunities along with competitive salaries and comprehensive benefits. Akorn is an Equal Opportunity Employer. M/F/V/D. Job ...
    Full job description at Monster

    Posted 3 days ago

  • Regulatory Affairs SpecialistEmd(Boston North, Massachusetts)

    Merck Millipore is a Life Science leader providing cutting-edge technologies, tools, and services for bioscience research and biopharmaceutical manufacturing. As a strategic partner, we collaborate with customers to confront the world's challenging human health issues. From research through development to production, our scientific expertise and innovative solutions help customers tackle their mos...
    Full job description at Monster

    Posted Today

  • Quality & Regulatory Affairs SpecialistPhilips(Cleveland, Ohio)

    Challenge Advanced Diagnostic Imaging (ADI) Regulatory Affairs provides regulatory leadership for Computed Tomography (CT), Magnetic Resonance Imaging (MRI), and Nuclear Medicine (NM) (PET/CT and SPECT) product lines. We build and deliver on competitive regulatory strategies. We work directly with regulatory agencies to achieve best possible outcomes. We are responsible for the coordination and pr...
    Full job description at Monster

    Posted 2 days ago

  • Senior Regulatory Affairs SpecialistVerathon(Seattle, Washington)

    Senior Regulatory Affairs Specialist - Verathon® Verathon® is looking for a Senior Regulatory Affairs Specialist to become the newest member of the QA/RA Team located in our Bothell, WA headquarters. The Senior Regulatory Affairs Specialist is responsible for the preparation and coordination of documentation dossiers for regulatory submissions, license renewals, annual registrations and approvals ...
    Full job description at Monster

    Posted Thu 10th July

  • 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 Fri 18th July

  • Regulatory Affairs SpecialistReal Staffing(Tucson, Arizona)

    Key Features - Assist in activities associated with regulatory approval of in vitro diagnostic medical devices in global markets. - Assist in submission activities for a variety of device regulatory approvals including the CE mark, US premarket approvals (PMAs), US premarket notifications (510(k)s), post-approval reports, export certificates, establishment registrations and listings, etc. - Acquir...
    Full job description at Monster

    Posted Tue 5th August

  • Regulatory Affairs SpecialistThe Judge Group(Anaheim/Huntington Beach, California)

    Our client is currently seeking a Regulatory Affairs Specialist in the Cypress, CA area. Summary Provide pre-market regulatory strategy and implementation to ensure regulatory approval objectives that support commercial initiatives for new and modified products. Supports applicable regulations including Local, State, Federal and/or International requirements. ESSENTIAL DUTIES & RESPONSIBILITIES Re...
    Full job description at Monster

    Posted Fri 8th August

  • Regulatory Affairs SpecialistMevion Medical Systems Inc(Framingham/Worcester, Massachusetts)

    Job duties and responsibilities: The Regulatory Affairs Specialist is responsible for identifying, evaluating, and ensuring meaningful compliance with all applicable laws, regulations, and standards. Efforts to ensure company compliance shall be inherently established within the company’s Quality System, the Mevion Business Management System. All RA/QA personnel shall seek to develop a quality and...
    Full job description at Monster

    Posted Fri 8th August

  • Senior Regulatory Affairs SpecialistTop Source Talent, LLC(Boulder/Fort Collins, Colorado)

    Sr Regulatory Affairs Spec Requisition 93994 Category Regulatory Affairs and QA Business Surgical Technologies Division RTG ST-Surgical Navigation Location USA-CO-Louisville Relocation Relocation eligibility to be determined Job Type Full Time - Regular Exempt/Non-Exempt Exempt Shift First Travel Percentage less than 10% Experience Required 7 years Education Required Bachelors Degree Position Desc...
    Full job description at Monster

    Posted Wed 13th August

  • Regulatory Affairs SpecialistLDR Spine(Austin, Texas)

    LDR, a spine medical device company offering exclusive spinal implant technologies for both non-fusion and fusion applications, is seeking a dependable, adaptable, professional individual to serve as Regulatory Affairs Specialist in our Austin Texas Corporate Headquarters, reporting to the Regulatory Affairs Project Manager. Responsibilities: Must work to ensure that LDR Spine is in compliance wit...
    Full job description at Monster

    Posted Wed 13th August

  • Senior Specialist Regulatory Affairs(St. Paul, Minnesota)

    Specialist Sr., Regulatory Affairs (St. Paul, Minnesota) Description Our client, a Global Medical Device company, is seeking three experienced, high caliber Sr. Regulatory Affairs Specialists: · Position 1: Has Previous regulatory submissions experience in Latin America. Spanish proficiency ideal · Position 2: Has previous regulatory submissions experience in Asia Pacific. Japanese, Chinese, Korea...
    Full job description at Monster

    Posted Mon 18th August

  • Regulatory Affairs /Quality Control SpecialistMarkwins International Corporation(Los Angeles, California)

    Markwins, a leading cosmetics and accessory company, is seeking an experienced Regulatory Affairs /Quality Control Specialist based in the City of Industry headquarters. Essential Functions · Provide regulatory support for cosmetic products on a domestic and international level with emphasis on the U.S., Canada, and EU. · Work with consultants and internal company personal to register facililities...
    Full job description at Monster

    Posted Mon 18th August

  • Regulatory Affairs Specialist - Job#: 14-01409TalentOptions(Southern, New Hampshire)

    Our client in Portsmouth,NH is looking for a Regulatory Affairs Specialist. This is a long term consulting position. If interested, Please apply to this ad Job Title: Regulatory Affairs Specialist Job Location: Portsmouth, NH Job#: 14-01409 REQUIRED QUALIFICATIONS: Bachelor's Degree required + 7 years medical device experience and work experience in regulatory affairs (less exp. required with high...
    Full job description at Monster

    Posted Mon 18th August

  • Regulatory Affairs SpecialistAdecco Technical(South Bend, Indiana)

    . A Regulatory Affairs Specialist job inWarsaw, IN is available courtesy of Adecco Engineering and Technology. Must have experience with FDA regulations to be considered for the position. Must be able to lead in the development of dossiers for registration of products in countries outside theUnited States. Regulatory Affairs Specialist job responsibilities include: • Contribute to the FDA regulato...
    Full job description at Monster

    Posted Wed 20th August

  • Senior Regulatory Affairs Specialist(Salem, Oregon)

    Senior Regulatory Affairs Specialist Seeking an experiencedSenior Regulatory Affairs Specialistto join our team in Corvallis, Oregon.This position will report directly to the VP of Regulatory Affairs. The successful candidate will be responsible for implementing regulatory strategies for the company and other acquired products in accordance with domestic and international regulations and guidance....
    Full job description at Monster

    Posted Wed 20th August

  • Senior Regulatory Affairs Specialist (Product Stewardship)The Richmond Group USA(Richmond, Virginia)

    Our client is a world class manufacturer which has experienced tremendous growth during the past decade and reinvesting in its business on a global scale. Due to their continued expansion, we have been engaged to identify a Senior Regulatory Affairs Specialist (Product Stewardship) to apply a robust knowledge of international regulatory and compliance challenges faced by manufacturing, supply chai...
    Full job description at Monster

    Posted Thu 21st August

  • Regulatory Affairs Specialist / 14-988Volcano Corporation(San Diego, California)

    Position Description: About Volcano We are revolutionizing the medical device industry with a broad suite of technologies that make imaging and therapy simpler, more informative and less invasive. Our products empower physicians around the world with a new generation of analytical tools that deliver more meaningful information - using sound and light as the guiding elements. Founded in cardiovascu...
    Full job description at Monster

    Posted Fri 22nd August

  • Regulatory Affairs SpecialistSterling Life Sciences(Mankato/Rochester, Minnesota)

    We are on the lookout for a driven individual with a passion for the medical device industry. One of our clients is looking to add a strong Regulatory Affairs Specialist to their team: 1) Plan, undertake and oversee product trials and regulatory inspection 2) Ensure that quality standards are met and submissions meet strict deadlines 3) Review product conformance and ensure compliance 4) Implement...
    Full job description at Monster

    Posted Sat 23rd August

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