Regulatory and quality management consultant for medical device market entry.
Review and optimize regulatory compliance and quality systems for a medical device company entering the South African market. The role involves gap analysis, process improvement, contract evaluation, and stakeholder advisory across international distribution networks. Requires deep medical device regulatory expertise, ISO 13485 knowledge, and experience with international supply chain risk assessment.
Found at a specialist agency · listed 24 October 2026 · InsideJobs links you to the original posting.