Back to jobsMinimum 3 years of expertise in quality management systems and regulatory compliance (ideally in in-vitro diagnostics or medical devices)
Hands-on experience in audits, Post Market Quality, supplier and distributor quality management (especially ISO9001)
The ability to work independently while influencing and supporting cross functional teams
Strong analytical capabilities with a solution-oriented mindset
A passion for continuous improvement and high-quality standards
Excellent communication skills, including strong international communication competencies
Experience supporting internal and external audits
Strong sense of ownership and accountability
Having a Regulatory Affairs and/or Compliance background is a strong asset, including prior experience in product registration, licensing, and compliance processes
Turkish and English proficiency
