Regulatory Affairs Specialist Jobs

Sort by: Date | Relevance

  • 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

  • Corporate Regulatory Affairs SpecialistNCH Corporation(Dallas, Texas)

    Job ID: 4336 Position Description: NCH is established, yet growing, and we need to attract top talent to support our overall business strategy. We are currently looking for a Corporate Regulatory Affairs Specialist who has the ability to partner with multiple internal departments, ensuring that our products comply with all federal, state and local regulations. This person will focus their efforts ...
    Full job description at Monster

    Posted Mon 28th July

  • 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 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 SpecialistAdecco(Los Angeles, California)

    Description: A local leading organization is currently seeking an experienced Regulatory Affairs Specialist for their Nutritional Pharmaceutical Industry in Northridge for a long-term temporary to hire opportunity. If you meet the qualifications listed below – Apply Now! The Regulatory Affairs Specialist is responsible for ensuring that all domestic and international regulations are met, helps est...
    Full job description at Monster

    Posted Thu 7th 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

  • 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 Mon 11th 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

  • 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 Thu 14th 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 3 days ago

  • 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 3 days ago

  • Regulatory Affairs Specialist JobYoh(Atlanta, Georgia)

    Company: Yoh Regulatory Affairs Specialist needed for a contract opportunity with Yoh's client located in Roswell, GA. The Big Picture - Top Skills You Should Possess: - Experience with US (510Ks) - Regulatory Affairs experience Latin America / International (Generating Dossiers and Obtaining Legalizations) What You'll Be Doing: - Support regulatory compliance throughout the organization by perfor...
    Full job description at Monster

    Posted Mon 4th 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

  • 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 2 days ago

Regulatory Affairs Specialist Job Search Tip

Specific job titles and duties vary widely within the clerical industry based on education, experience, and company position. High school graduates are eligible for basic entry-level positions. With more training in certification programs or college level courses, clerical staff can take on more responsibility and more job duties. Clerical jobs can be full-time, part-time or even flexible schedules, including telecommuting if the bulk of the work can be done via computer and transmitted back to the office.

Learn how to write a resume, find relevant resume samples, read through resume help, and then create your resume on Monster's resume builder.



Find local jobs
Keywords
Location

Powered by Monster