How do they match: Regulatory Affairs Specialists

  • Regulatory Affairs Specialists

  • Clinical Quality Assurance Specialist
  • Compliance Specialist
  • Drug Regulatory Affairs Specialist
  • Product Safety Specialist
  • QA Specialist
  • Quality Assurance Specialist
  • Quality Assurance Documentation Specialist
  • RA Specialist
  • Regulatory Specialist
  • Regulatory Affairs Specialist
  • Regulatory Compliance Specialist
  • Research Compliance Specialist
  • Research QA Specialist
  • Research Quality Assurance Specialist

  • 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.

  • Specialize in regulatory issues related to agriculture, such as the cultivation of green biotechnology crops or the post-market regulation of genetically altered crops.
  • 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.
  • Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.