Development Quality Manager / MUB
2011-09-06
Our client, leading worldwide pharmaceutical company is looking for a Development Quality Manager. Development QM is responsible for Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPvP) oversight and for assuring the quality and compliance of Development and Medical Affairs (MA) projects, products and programs (Phase I through Phase IV). Ensure in direct collaboration and partnership with CPO Medical department (including GenMed, Oncology, DS&E, DRA and MA) the implementation of the company Quality Manual and Quality Management System in the CPO Medical Department to achieve a high level of quality and compliance.
Key Performence Indicators:
Local GCP/PV Quality System in place and continously updated, as required. GCP/PV risk proactively identified and effectively mitigated. Training conducted according to program.
Ideal beckground:
Degree in life science or related fields. English fluent in speaking and writing. Minimum 5 years experience in the pharmaceutical industry in a relevant field such as quality assurance, registration, clinical development or a directly related area.
In case of interest please send your CV to Marcela Bukacova at bukacova@hays.cz
