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QM Officer Sant Joan Despí Spain,  

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.


08970 Sant Joan Despí Barcelona Spain

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