Quality Engineer

We are looking for Quality Engineers with 5–7 years of experience to support quality and compliance activities for Medical devices domain on a 1-year contract. Job Description: Develop, implement, and maintain quality systems in accordance with ISO 13485, FDA 21 CFR Part 820, and EU MDR requirements. Support design control activities, including risk management, verification/validation, and design transfer. Conduct root cause analysis and corrective/preventive actions (CAPA). Collaborate with c…