Future Lead Auditor for ISO 13485

TL;DR

Future Lead Auditor for ISO 13485 (Medical Devices): Transition into an Auditor role via the Auditor Academy program with training, real-world projects, and mentorship to achieve a globally recognized qualification with an accent on medical device compliance standards. Focus on leveraging industry experience in R&D, manufacturing, clinical applications, and testing to conduct ISO 13485 audits.

Location: Cape Town or Johannesburg, South Africa

Company

hirify.global is the world's leading global assurance provider operating in over 150 countries with expertise in assessment, advisory, inspection, and cybersecurity services.

What you will do

• Participate in the Auditor Academy to gain skills, knowledge, and connections for a career in auditing.
• Work on real-world projects with mentorship from world-class experts.
• Collaborate with global internal teams on problem-solving and communication.
• Commit to continuous professional development and own your learning journey.

Requirements

• BSc degree, higher diploma or equivalent in biomedical science, microbiology, chemistry, biochemistry, bioengineering, human physiology, medicine, pharmacy, physics, or biophysics.
• Minimum 4 years full-time work experience in medical device industry, including 2 years in R&D, manufacturing, clinical application, compliance testing, performance testing, evaluation studies, or clinical trials.
• Effective communication in local language and English (verbal and written).

Culture & Benefits

• Supportive environment for career transitions with investment in learning and development.
• Access to transformative training program tailored for success.
• Inclusive culture embracing diverse perspectives for a safer, sustainable future.
• Pre-employment checks including right to work, ID, employment history, education, and criminal records as per local law.