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To lead and proactively manage all regulatory activities associated with development, registration and maintenance of Drug Master Files according to current international regulatory requirements.
Good Leadership and communication skills
Organized
Wide and open view
Self- learning capabilities
Individual work ability
Comprehensive work
High writing skills
Meeting work target time lines
Accuracy
Readiness to work when requiredInitiative
Self-motivated
Time management
English good professional level, both in writing and speaking
High degree in relevant field, e.g. chemistry/biochemistry/biology or biotechnology
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