Quality Engineer, Manchester


Daily tasks will include the review of batch documentation, specifications, test methods, NCR, CAPA and complaints systems and documentation, while reviewing existing validations,and recommending and implementing improvements. Good organisation skills are paramount in order to help deliver project goals to agreed timelines and budget.


A suitable individual would be degree qualified with a minimum of 2-3 years QA experience in the Medical Device or Pharmaceutical manufacturing environment, expertise in preparing documentation that complies with ISO 13485 standards (mandatory), and hands on validation experience. Use of quality statistics for process improvement and experience in in Six Sigma is a bonus.


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