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Do you have the right mix of excellent scientific and analytical skills, together with the ability to interpret and assess complex regulatory and Good Manufacturing Practices (GMP)...
Planning and co-ordinating Certification of Suitability (CEP) dossiers compliance according to the European Pharmacopea monographs (‘CEP dossiers’) and other activities, with...
You lead cross-functional teams to facilitate new product introduction, process transfers, validation and advance process technologies. You will oversee technical support for...