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QM Officer - Spain  

Medichem (company)

Posted on : 03 May 2017

Project Description

Main responsibilities: 
  • Review validation protocols and reports 
  • Ensure that any deviation from procedure to cGMP is investigated and documented according to procedures 
  • Ensure compliance and adhere to Company policies and procedures, quality standards, H&S regulations as well as relevant US, EU and international GMP requirements for pharmaceutical products for human consumption.  

Minimum Requirements: 
  • Be in possession of a University Degree in Pharmacy, Biology or Chemistry 
  • Preferably have experience in a similar role 
  • Have excellent organisation and communications skills  

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