Key Responsibilities:

Regulatory & Compliance (Core Focus)

• Maintain and enhance the Quality Management System (QMS) in line with ISO 13485.
• Ensure all departments comply with ISO procedures, keeping documentation audit-ready.
  Manage SAHPRA license compliance and update medical device files with current certifications.
  Oversee corrective actions, risk assessments, and supplier database updates.
  Liaise with suppliers, customers, and industry bodies to ensure regulatory compliance.
  Assist in product registrations, failure reporting, and returns processing.

Operations & Stock Control

•  Support import/export compliance and assist with stock takes & cycle counts.
• Update supplier price lists and manage custom product procurement.

Financial & HR Support

• Assist with fleet management, creditor payments, and financial reporting.
• Maintain employee records, leave registers, and recruitment coordination.