Quality Controller
Job in
Jeddah, Saudi Arabia
Listed on 2026-09-25
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
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
- 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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