Tarin Rahman

I am a quality engineer with three years' experience in medical device production, experienced in GMP environments, QMS maintenance, and regulatory compliance with ISO 13485, ISO 14971, FDA, EU, and Health Canada. I have driven measurable quality improvements—reducing non-conformances by 40%, cutting waste 35%, halving product complaints, and supporting a $15.74M revenue increase while maintaining zero major non-conformances.

I lead risk management, FMEA, CAPA, internal and supplier audits, and DHR review, and I design and validate device prototypes using SolidWorks with manufacturing tolerances of ±0.05mm. I am proficient with MasterControl, Minitab, MATLAB, Python, and Lean methods, and hold certifications including CAPM and Health Canada regulatory training to support robust, audit-ready quality systems.