Guarantee that current pharmaceutical standards, legal regulations and approved registrations are implemented for production and controlling of Third Party manufactured products
Supervise entrusted products through the entire life cycle with regard to pharmaceutical quality
Initiate, coordinate, supervise and assess activities carried out by relevant expert team for product quality
Act as internal and external contact for issues concerning pharmaceutical quality
Coordination and controlling of all GMP relevant documents
Support the Quality Relationship Manager
Maintain regulatory compliance of suppliers with EMA authorities
Review and authorize Master Documents to assure supplier regulatory compliance
Support preparation and execution of regular audits/ technical visits
Requirements
Bachelor’s degree in Pharmaceutical/Natural/Engineering science or related field
3+ years’ experience in quality control / analysis, production and / or quality assurance
Must have working knowledge of cGMPs and applicable international regulations/guidelines
Strong computer skills including MS Office, TrackWise and SAP
Good command of the written and spoken English language