In order to prove safety, quality and effectiveness to the authorities, Regulatory Affairs employees combine extensive and profound pharmaceutical know how and in depth knowledge of legal details and requirements. A Regulatory Affairs Manager works intensively with all areas of the company and has to harmonize different ways of thinking and interests with the regulatory requirements in the entire development and marketing process. Inquiries by the authorities or even delays in the approval process often cost companies a lot of money, so the experts in this area are often subject to tight deadlines. These diverse requirements need a high level of personal competency and a strong ability to deal with internal and external contact persons. The challenge is to match these in the recruitment process with the particular requirements of the position.
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