...manufacturing of sterile drug products
~ Experience in parenteral compounding and filling
~ Involvement in deviations CAPAs and risk assessmets (FMEA)
~ Understanding of process engineering analytical and regulatory aspects of sterile drug product manufacturing...
Empfohlen
Vollzeit
...manufacturing equipment room utilities and cleaning validation program
Review and approve qualification and validation documentation (e.g risk assessment protocol report)
Evaluate Review and approve deviation discrepancy and changes control that occurred during...
Empfohlen
Vollzeit