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Senior Regulatory Affairs Manager (m/w/D)

Ort: AT
Unternehmen: Merck Gesellschaft mbH
Vertragsart: Unbefristet
Arbeitszeit: Teilzeit
karriere.at
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Senior Regulatory Affairs Manager (m/w/D)

Part time 20 h/w - limited until end of December 2025

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role:

Ready to join our Austrian affiliate? We are looking for a Regulatory Affairs Market Specialist located in Vienna. In this position you would be the main point of contact for the Austrian Health Authorities. You will perform as the local business partner to different stakeholders of the local organization. You will be responsible for key regulatory activities, including any required Health Authority interactions for the Austrian organization, to ensure maintenance of Marketing Authorizations for the company's product portfolio. Your tasks will be the life cycle management of the marketed product as well as registration of new compounds, including possible Early Access Programs for new assets and relevant support for clinical trials as applicable.

Additionally, you will support the Swiss team on maintenance and life-cycle activities. An outstanding possibility, combining the expertise of different countries. You will be part of a cluster team, supported via the knowledge and expertise of the cluster team members.

The position is limited to one year and is preferably part-time (50%). The position can be filled from Austria or Germany.

Who you are:

* You completed a master's degree in life sciences (pharmacy, chemistry, biology, or related discipline)
* You have at least 4 years of experience in the pharmaceutical industry and have the technical regulatory knowledge of Austrian regulatory requirements
* Experience and knowledge in review of promotional material or Regulatory experience in Switzerland would be an asset
* You understand business needs, think strategically, and develop risk mitigation strategies
* Excellent English and German language
* You are a standout colleague with a high level of dedication and a strong willingness to perform.

The annual salary depends on your qualifications and previous experience. The salary range for this position starts from 50.000EUR/year.

What we offer:

We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!
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