My client is a leading pharmaceutical company which is globally involved in the production of pharmaceutical products.
Role Description
My client is looking for a new Manager of Regulatory Affairs for his office in Munich.
Responsibilities
Establishment of CMC requests Responsible for establishment of modification and extension applications Records management in eCTD Working on product information sheets Interaction with national and foreign authorities Accountable for national and international approval procedures Handling of internal interfaces
Requirements
Studies completed with a science degree Experienced in the area of drug approval Works reliably and independently Fluently in English Collaborative and communicative skills Engagement and goal-oriented behavior
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