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Regulatory Affairs Project Manager

rapidai · 30+ days ago
Negotiable
Full-time
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Position Duties And Responsibilities

  • Assemble, distribute, store, track and retrieve information pertinent to the regulatory process, including the regulatory submissions process 
  • Author and publish electronic submission
  • Manage requests from foreign government and/or distributors as needed
  • Research, analyze and communicate information pertaining to the appropriate regulatory pathway for new or modified products
  • Provide regulatory direction to development project teams as a core team member; helps develop regulatory strategy for new products
  • Evaluate risk of proposed regulatory strategies; may offer solutions
  • Review proposed labeling for compliance with applicable global regulations
  • Review and evaluate promotion and advertising material for compliance with applicable regulations
  • Review proposed product changes for impact on regulatory status of the product
  • Communicate with regulatory and governmental agencies
  • Apply FDA regulations to business practices and provides regulatory input, advice and guidance to design teams
  • Assist quality team – including but not limited to training and document control
  • This position does not have direct reports.
  • Perform any other related activites assigned by reporting manager.

Education, Experience, And Qualification

  • Strong writing, communication, and interpersonal skills
  • Strong attention to detail; ability to multi-task and balance competing priorities
  • Knowledge of overall business environment, the SaMD industry, and the marketplace
  • Ability to learn and stay abreast of regulations pertinent to medical devices
  • Ability to building relationships between Regulatory Affairs and other areas of the
  • organization: ability to communicate effectively at all levels
  • Knowledge of FDA, EU, and other regulatory body regulations
  • Ability to identify risk in Regulatory strategies
  • Strong problem-solving skills
  • Bachelor’s degree required
  • A minimum of 2-5 years of experience in SaMD or medical device industry
  • Regulatory Affairs Certification (US or EU) preferred

Last updated on Sep 1, 2024

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