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
  • Risk and Compliance Analyst

  • 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.
  • Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review.
  • Direct the collection and preparation of laboratory samples as requested by regulatory agencies.
  • Prepare or direct the preparation of additional information or responses as requested by regulatory agencies.
  • Review adverse drug reactions and file all related reports in accordance with regulatory agency guidelines.
  • Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.

  • Investigate system, equipment, or product failures.
  • Communicate with government agencies.