the P&ID system.
guidelines in conjunction with the Kassel Quality Department regarding the returns of genuine parts through
within the P&ID system. Quality Assurance: Adhere to the Department Quality Plan, ensuring all tasks
registered within the Quality Management system (Quality Department) as stipulated per Quality Procedures. To
registered within the Quality Management system (Quality Department) as stipulated per Quality Procedures. To
ARS Contracts as well as assisting the Quality Review Department Assess patient files to ensure that all
Quality Manager-Roodepoort-R50 000ctc Quality Qualification and minimum 5 years’ experience in a production/operations environment. Must have working experience in laboratory testing & reporting, in a management position in a manufacturing environment. Must have health, safety and environmenta
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effectively.