Our client is a professional Pharmaceutical organization, based in Basel-Stadt Switzerland.
Our client is a multinational company specialized in manufacturing of pharma and other products.
In this role you will be responsible for managing 10+ manufacturing sites in Europe from a quality perspective.
- Making sure that Plants are in compliance according to relevant guidelines such as cGMP - Representing European plants on Quality matters - End responsible for topics such as CAPA, root cause analysis, complaint handling - Internal & External audit responsibilities - Responsible for KPI measurement and trend analysis and implementation - Continuous improvement
- Educated in Chemistry or Chemical Engineering (Bachelor, Master, PhD) - At least eight years of experience in chemically related manufacturing for specialty chemicals or pharma products - Strong knowledge of GMP and other industry guidelines - Experienced auditor - Knowledge of continuous improvement - Able to travel extensively - Excellent language skills in English and preferably other Western European languages such as German
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact admin admin.
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