You will support the Quality Manager and will be in charge of: – coding, issuing, distributing documents with controlled distribution; – perform training relating to procedures or audit findings; – carry out general training on quality and GMP; – draw up the procedures relating to the quality area; – define the official codes for the documentation; – follow and file anomaly management practices (Deviations, non-conformities and improvement actions relating to systems and / or processes;
Job Requirements:
Diploma or Degree in Pharmaceutical, chemical, biological or similar disciplines and at least two years’ experience in a similar role. Required knowledge of GMP, HACCP and ISO 9001 principles, problem solving skills,
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