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Projektbeschreibung
REFERENZNUMMER:
296003/11
IHRE AUFGABEN:
-Responsible for maintenance and revision specifications and methods for products manufactured at CMO's including assessment and implementation of new regulatory requirements
-Support for analytical methods, stability protocols and other laboratory impacting activities
-Review release testing data to support qualifications of CMO for raw data review
-Support in quality control and stability related topics, investigations and issues
-Reviews and assesses QC activities at CMO's against cGMP's
IHRE QUALIFIKATIONEN:
-M.S. in Science or equivalent
-Profound experience in Quality Control or analytical development including Laboratory experience
-Strong knowledge of global pharmaceutical industry
-Flexibility in work hours and travel to meet business objectives
-Ability to speak English and another European language
WEITERE QUALIFIKATIONEN:
Quality manager
296003/11
IHRE AUFGABEN:
-Responsible for maintenance and revision specifications and methods for products manufactured at CMO's including assessment and implementation of new regulatory requirements
-Support for analytical methods, stability protocols and other laboratory impacting activities
-Review release testing data to support qualifications of CMO for raw data review
-Support in quality control and stability related topics, investigations and issues
-Reviews and assesses QC activities at CMO's against cGMP's
IHRE QUALIFIKATIONEN:
-M.S. in Science or equivalent
-Profound experience in Quality Control or analytical development including Laboratory experience
-Strong knowledge of global pharmaceutical industry
-Flexibility in work hours and travel to meet business objectives
-Ability to speak English and another European language
WEITERE QUALIFIKATIONEN:
Quality manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges