Master's student in Biomedical Engineering with a focus on quality management systems for medical devices, regulatory compliance, and risk management. Experienced in ISO 13485, MDR requirements, and risk management principles according to ISO 14971. Practical experience in quality documentation, CAPA processes, and technical documentation management in the medical technology field.
Cutera Aesthetics • Islamabad, Pakistan
Managed quality-related documentation including installation and maintenance reports according to ISO 13485. Supported internal compliance audits and ensured traceability of service records for medical devices.
Rawalpindi Institute of Cardiology • Rawalpindi, Pakistan
Assisted in the calibration, testing, and validation of medical devices according to QA protocols. Documented service, maintenance, and performance testing data according to hospital quality procedures.
Micromed Medizintechnik GmbH • Germany
Supported the preparation, review, and continuous improvement of quality assurance agreements with suppliers and partners to ensure regulatory and contractual compliance.