Job Details
Skills And Tools:
Job Description
Develop and implement quality control procedures and inspection plans for medical devices, Telecom products, and Powered Products.
Perform and oversee routine inspection, verification, and testing processes throughout the product lifecycle.
Validate and calibrate tooling, testing equipment, and measurement systems according to international standards.
Ensure conformity to ISO 13485, ISO 9001, CE, FDA CFR 820, MDR 2017/745 and other regulatory standards.
Prepare complete quality documentation including control plans, CAPA reports, failure analysis reports, and risk assessments.
Apply principles of Total Quality Management (TQM) to build a culture of excellence and continuous improvement.
Lead quality improvement projects using Lean, Six Sigma, and Kaizen practices.
Monitor quality metrics and KPIs, evaluate trends, and provide insights to management.
Ensure compliance with regulatory agency requirements such as FDA, EU MDR, and telecommunications authorities.
Participate in quality audits including supplier and certification audits
Job Requirements
Bachelor’s degree in Electronic Engineering, Biomedical Engineering, Communications Engineering, Mechanical Engineering, Scince or related field.
Minimum 1–3 years of experience in quality control within medical devices or electronics manufacturing.
Hands-on knowledge of ISO 13485, ISO 9001, and TQM frameworks.
Experience with design validation, verification testing, and risk management (e.g., FMEA, FTA).
Familiarity with telecom certification standards (e.g. CE, RoHS) is a plus.
Strong analytical and statistical skills using tools like Minitab, SPC, or JMP.
Excellent communication and report-writing skills in English.
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