How do they match: Regulatory Affairs Specialists

  • Regulatory Affairs Specialists

  • Drug Regulatory Affairs Specialist
  • Regulatory Affairs Analyst
  • Regulatory Affairs Associate
  • Regulatory Affairs Consultant
  • Regulatory Affairs Coordinator
  • Regulatory Affairs Manager
  • Regulatory Affairs Specialist
  • Regulatory Affairs Strategist

  • Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations. May compile and prepare materials for submission to regulatory agencies.

  • Coordinate, prepare, or review regulatory submissions for domestic or international projects.
  • Determine the types of regulatory submissions or internal documentation that are required in situations such as proposed device changes or labeling changes.
  • Identify relevant guidance documents, international standards, or consensus standards.
  • Monitor national or international legislation on ozone-depleting substances or global warming.
  • Obtain and distribute updated information regarding domestic or international laws, guidelines, or standards.
  • Participate in internal or external audits.
  • Prepare responses to customer requests for information, such as product data, written regulatory affairs statements, surveys, or questionnaires.