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IVD Regulatory Affairs Specialist

Company: Kelly Services
Location: Sunnyvale
Posted on: April 11, 2021

Job Description:

Title: Regulatory Affairs SpecialistLocation: Sunnyvale, CA (This will be an onsite position)Term: 1 year contract opportunityThe Regulatory Affairs Specialist will prepare the regulatory submissions and interact with Distributors, Regulatory Agencies and Health Authorities to obtain and maintain product approvals.ESSENTIAL JOB RESPONSIBILITIES:

  • Prepare regulatory submissions for countries with focus on Latin America region--
  • Communicates with in-country Regulatory Affairs--personnel to facilitate global clearances/approvals.
  • Coordination with department personnel from regulatory, quality, and manufacturing sites, sales and marketing.
  • Interact with global regulatory leaders and peers to expedite approval of pending registrations.
  • Organizes and maintains--files such as Responsibilities Matrix, Certificates from Notified Bodies CFS and CFG and other RA related material.
  • Regulatory review and approval of design, manufacturing, labelling, packaging-related changes in compliance with applicable regulations and providing Regulatory Change Assessments through RCA .
  • Prepare formal written reports, PowerPoint presentations, and documents for distribution within work unit and regions.Education and Experience in years :
    • Bachelor's degree in Life Science or related field with 2+ years of Quality or Regulatory experience -OR-
    • Master's degree in in a Life Science or related field with 1-2 years of Quality or Regulatory--work experienceKnowledge and skills:
      • Demonstrate in-depth understanding of advanced technical/scientific principles that relate to multiple, diverse, and or complex product lines or manufacturing processes
      • Ability to interpret subjective and complex aspects of specific regulations and has thorough understanding of multiple sets of associated regulations
      • IVD product experience is highly preferred
      • Prior knowledge of different databases like--Trackwise,--Agile documentation system is preferred.
      • Experience in regulatory/Quality or related departments within an IVD or medical device industry
      • Fluency in Spanish preferredWhy Kelly--?Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.About Kelly--At Kelly, we're always thinking about what's next and advising job seekers on new ways of working to reach their full potential. In fact, we're a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world. Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.]]

Keywords: Kelly Services, Sunnyvale , IVD Regulatory Affairs Specialist, Other , Sunnyvale, California

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