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Quality Controller

Job in Jeddah, Saudi Arabia
Listing for: Zhende Middle East
Full Time position
Listed on 2026-09-25
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA, Quality Engineering
Salary/Wage Range or Industry Benchmark: 150000 - 190000 SAR Yearly SAR 150000.00 190000.00 YEAR
Job Description & How to Apply Below

Job Responsibilities

  • Perform incoming in-process and final quality inspections of raw materials components semi-finished products and finished medical device products according to approved specifications and inspection procedures
  • Conduct routine quality inspections and testing during the manufacturing process to ensure products meet established quality standards and specifications
  • Verify product dimensions appearance functionality packaging labeling and other applicable quality requirements
  • Identify record and report quality defects deviations and non-conformities in a timely manner
  • Isolate and properly identify non-conforming materials or products and follow the established procedures for non-conforming product control
  • Maintain accurate and complete QC inspection records test results checklists and other quality-related documentation
  • Support investigation and analysis of quality issues and assist in implementing corrective and preventive actions CAPA
  • Ensure all quality control activities comply with company procedures applicable Saudi regulations and relevant medical device quality management system requirements
  • Follow company requirements related to ISO 13485 GMP document control traceability and product quality management
  • Perform other quality-related duties assigned by the QC Supervisor or Quality Manager
Requirements & Qualifications
  • Bachelor’s degree or diploma in Quality Management, Medical Devices, Biomedical Engineering, Mechanical Engineering, Industrial Engineering, Chemistry, Biology, or a related field.
  • Previous experience in quality control or quality inspection, preferably in medical device, pharmaceutical, healthcare, or other regulated manufacturing industries.
  • Knowledge of medical device quality control processes and inspection methods is preferred.
  • Familiarity with ISO 13485, GMP, quality management systems, and non-conforming product control is highly preferred.
  • Good understanding of basic quality tools and methods, such as inspection plans, sampling, defect classification, root cause analysis, and CAPA.
  • Good problem-solving and analytical skills.
  • Good documentation and record-keeping skills.
  • Ability to work independently and effectively in a manufacturing environment.
  • Good communication and teamwork skills.
  • Good command of English, both written and spoken.
  • Basic computer skills, including Microsoft Office (Word, Excel, Outlook).
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