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Projektbeschreibung
REFERENZNUMMER:
332333/11
IHRE AUFGABEN:
-Provide Global Product Development Medical Affairs (PDMA) staff with compliance support to ensure that all medical affairs activities are conducted in accordance to the internal SOPs, guidelines, policies and health authority regulations
-Ensure staff are trained on internal controlled documents and international regulations
-Coordinate the learning management system
-Implement quality management processes
-Provide compliance support
-Promote cross-functional and affiliates communication
IHRE QUALIFIKATIONEN:
-Professional experience within the pharmaceutical industry
-In-depth knowledge of ICH, GCP, SOPs and regulatory requirements
-Experience in quality risk management or quality management
-Strong analytical and and decision making skills
-Fluency in written and verbal English
WEITERE QUALIFIKATIONEN:
Quality manager
332333/11
IHRE AUFGABEN:
-Provide Global Product Development Medical Affairs (PDMA) staff with compliance support to ensure that all medical affairs activities are conducted in accordance to the internal SOPs, guidelines, policies and health authority regulations
-Ensure staff are trained on internal controlled documents and international regulations
-Coordinate the learning management system
-Implement quality management processes
-Provide compliance support
-Promote cross-functional and affiliates communication
IHRE QUALIFIKATIONEN:
-Professional experience within the pharmaceutical industry
-In-depth knowledge of ICH, GCP, SOPs and regulatory requirements
-Experience in quality risk management or quality management
-Strong analytical and and decision making skills
-Fluency in written and verbal English
WEITERE QUALIFIKATIONEN:
Quality manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges
Hays
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Straße:
Willy-Brandt-Platz 1-3
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Ort:
68161 Mannheim, Universitätsstadt, Deutschland