0Head of the Department of Drug Approval and Safety (m/f/d)
Pharma Deutschland e.V. | Germany | 53xxx Bonn | Permanent position | Full time / Home office | Published since: 21.09.2026 on stepstone.de

Head of the Department of Drug Approval and Safety (m/f/d)

Branch: Public relations Branch: Public relations


Pharma Deutschland e.V. is the most important industry association of the pharmaceutical industry in Germany. He represents the interests of around 400 member companies, which in Germany is approx. 80,000 employees employ. The companies organized by Pharma Deutschland contribute significantly to ensuring the supply of both prescription-free and prescription-free medicines in Germany. Representation of manufacturers of medical devices and digital health applications is also part of the range of tasks of Pharma Deutschland. With its high level of expertise and expertise, Pharma Deutschland is close contact with politics, authorities and institutions in the healthcare sector as well as a strong link between the various stakeholders. For our office in Bonn, we are looking for a Senior Consultant (m/w/d)

Your tasks • Your profile • What we offer

As Head (m/w/d), you will lead the Department of Medicinal Approval and Security in a strategic and operational way. You report directly to the Managing Director of Science and agree with it on the strategic orientation of the department. Together with your team, you will support the field of medicine admission and drug safety as well as the associated committees and working groups and assist in the planning, organisation and implementation of further training events in the field of medicine admission and safety. Together with your team, you will actively and regularly inform our member companies about current developments and advise them on technical questions from the entire field of pharmaceutical authorisation and drug safety. You represent the concerns of our member companies with the support of your team to authorities. You actively work with the evaluation and commentation of legal and sub-legal requirements and regulations in the field of pharmaceutical authorisation and safety and work together with the team and the committees as well as working groups to develop proposals for the optimization and simplification of the above-mentioned requirements and regulations. You represent our colleagues in the field of pharmacovigilance in the technical support of coordination of risk-reducing measures for our member companies, e.g. the creation of red-hand letters.

You have successfully completed a study of pharmacy or other natural sciences and have very good knowledge of German and European licensing and drug safety legislation as well as regulatory guidelines. This knowledge has already been practically applied to companies in the pharmaceutical industry and have gained experience with structures and processes in the industry. You are distinguished by an efficient, structured and very careful way of working, are team-ready and enjoy cooperation in interdisciplinary teams. You will be happy to work in new topics quickly and quickly and solve questions flexibly, efficiently and targeted – keep in your versatile task You always have an overview. Sovereign appearance, discretion and loyalty are of course for you. You have very good knowledge of the German and English language in word and writing. You shall bring the necessary readiness to travel (D, EU) to the place. Safe handling of the common application software completes your profile.

We offer you a diverse and responsible activity in a pleasant working environment. An exciting task area in a motivated interdisciplinary team as well as a performance-oriented salary including additional social benefits (e.g. VWL, Ticket Plus, JobRad, occupational health insurance etc.) await you. There is the possibility of mobile work in the context of operating conditions. .

Location

ava Pharma Deutschland e.V.
53173  Bonn
Germany

The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.

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