Lead Auditor, ISO 13485

work closely with other internal teams across the Globe gain access to training, real-world projects, and mentorship collaborate to deliver quality assurance services Requirements BSc degree, higher diploma or equivalent in biomedical science, microbiology, chemistry, biochemistry or bioengineering, human physiology, medicine, pharmacy, physics or biophysics minimum of four years full-time work experience in a medical device related industry two years in research & development, manufacturing, or application of the device in a clinical setting collaboration, communication and problem solving skills commitment to continuous development able to communicate effectively in Local language and English (verbal, written)