Regulatory Affais Manager (m/w/d) in Mainz, full-time (RE

EUR60000 - EUR90000 pro Jahr + flexible Arbeitszeiten

Regulatory Affairs Manager (m/w/d)

in Mainz, full-time

Your responsibilities:

• Active participation and the regulatory support of development projects and development of new strategies and regulatory perspectives
• Preparation of EU approval documentation and regulatory assessment of EU-regulatory demands of non-generic drugs
• Authorization of European marketing procedures for pharmaceutical drugs and international projects
• Responding to inquiries from our national and international partners and authorities

Your profile:

• Successfully completed studies in natural sciences (pharmacy or chemistry)
• 3 years of professional experience, primarily in the field of non-generic products
• Good knowledge of the regulatory requirements for non-generic drugs in the EU and knowledge of the national and international regulatory requirements for the new marketing authorization and maintenance of pharmaceutical drugs
• Very good English and German skills
• Willingness to occasional travel

Please contact me if you would like to get further details regarding the role

Your contact:
Tatiana Panfilova
t.panfilova(at)realstaffing.com
0159/060 360 87
;

Regulatory Affais Manager (m/w/d) in Mainz, full-time (RE-33418383) 

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