Process and Validation Manager Technical Operations (m/f)

REFERENZNUMMER:

255308/11

IHRE AUFGABEN:

-Lead and supervise the validation team and be fully accountable for the process and cleaning validation/re-validation and material qualification programs team in accordance with regulations and GxP compliance
-Ensure that ongoing and pending tasks are accomplished and that projects are implemented while respecting the quality, time and cost targets
-Support the development, continuous improvement and harmonization of business processes, workflows, quality systems and procedural guidance in the area of the validation of manufacturing and cleaning processes

IHRE QUALIFIKATIONEN:

-University and/or college degree in biotechnology, pharmacy, process engineering, chemistry or equivalent
-Proven relevant professional experience in the field of manufacturing of drugs, pharmaceuticals or medicinal products preferably in an internationally operating company
-Experience in direct line management, staff leadership or team leadership
-Experience in dealing with authorities and official bodies, in particular during inspections
-Experience in the management of medium and large-scale projects
-Profound expertise in the validation of biotechnological or pharmaceutical manufacturing processes
-Fluent in French and English (spoken and written)

WEITERE QUALIFIKATIONEN:

Qualification/validation specialist, Quality manager