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Quality Supervisor

Dulex Lab
10th of Ramadan City, Sharqia

Quality Supervisor

10th of Ramadan City, SharqiaPosted 1 month ago
68Applicants for1 open position
  • 65Viewed
  • 15In Consideration
  • 50Not Selected

Job Details

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Job Description

  • Responsible for product quality throughout the manufacturing process.
  • Responsible for performing sanitation verification testing on equipment and other areas required.
  • Responsible for the correct recording and filing of all relevant record logs and documentation.
  • Ensures the correct recipe guidelines for products are met during processing.
  • Ensures and educates employees on GMP standards.
  • Collect product samples for Product Development, lab retains and the laboratory.
  • Perform inspections on Products, Equipment and Machinery.
  • Conducts checks on products and ensure all rules and regulations are followed and manage log books.
  • Monitors customer specifications to ensure proper weight and appearance of products produced.
  • Communicates products that do not meet specification or quality to the unit production manager.
  • Reports violations to management & to issue disciplinary action.
  • Inspect materials, products, or equipment to detect defects or malfunctions.
  • Performing pre and post-production quality checks and providing related reports accordingly.
  • Ensure that GMP Standards are followed properly in the Warehouse, Dispensing and manufacturing areas and during the manufacturing processes.
  • Ensure that sensory evaluation of finished products takes place as planned. 
  • Develop, maintain and audit sensory procedures in the Value Stream.
  • Ensure the hold and release system works effectively for the Value Stream for raw materials, packaging materials, semi-finished goods, finished goods on the Manufacturing shop floor.
  • Actively participate in investigations and complaints.
  • Actively participate in Daily and weekly Operation Meeting.
  • Performs other duties as assigned

Job Requirements

  • B.Sc. degree of Pharmacy, Engineering, Science equivalent level of education.
  • Strong knowledge and experience with ISO9001 and GMP.
  • More than 5 years of professional experience in Quality assurance in pharmaceutical industry.
  • Competent in the use of Microsoft Office (Word, Excel, and PowerPoint).
  • Self-motivated, Keen to learn, Smart worker, Lead and engage people, Communication skills, must be disciplined and well organized, attention to detail, flexibility.

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