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Quality Assurance

Quality Manager (Devices)

Details

  • Full-time permanent position
  • Site based in East Sussex
  • Competitive package
  • Global pharma company

The Role

  • The site Quality Manager  has direct responsibility for the site Quality system and Quality Leadership at the facility .
  • They will ensure that a site Quality Management System is maintained for product manufacturing, control, storage, and primary distribution processes in accordance with applicable  MDD regulatory requirements, ISO 13485, upcoming UKCA  , MDR and associated  Standards
  • Provide support & guidance  to the Brexit ,UKCA  and MDR projects as applicable

Full job description available on application

The Candidate

  • Experience in manufacturing Quality or Quality systems supporting a manufacturing site preferably in the Medical Devices field (minimum 3 years experience).
  • Qualified Lead Auditor  and statistical knowledge an advantage
  • Knowledge of applicable ISO Standards, Medical Device Directive and the Medical Device Regulation
  • Only candidates with existing right to work in the UK/EU will be considered

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