In the field of rare diseases the AOP Orphan team develops and investigates therapy options for patients with rare diseases – commitment and appreciation are the essence of our cooperative work.
AOP Orphan was founded in 1996 by Dr. Rudolf Widmann with the purpose of developing and producing therapy options for patients with rare diseases. The intention was to first introduce the product in Austria, then in European core countries of AOP Orphan, and finally in the international market.
After receiving your application documents we screen them carefully. Please give us at least two weeks’ time for this process. If your profile is a good match for the position, we will start the interview process.
As the selected candidate you will participate in our individualised introduction program from the start. We will pair you up with an experienced AOP buddy who will show you the ropes during your first few weeks.
Currently we are looking for ambitious candidates.
In addition to personal initiative, at AOP Orphan we look for a person’s willingness to contribute. Potential candidates should feel comfortable even outside their comfort zone and not identify themselves solely with their personal tasks as listed in their job description.
Ing. Dipl-Ing. (FH) Johannes Pilz | Program Coordinator
Individuality is not only a core aspect of our entrepreneurial activities - we give prime importance to individual development in the careers of our staff members. Depending on the performance and competence, we offer a variety of training and development options.
At AOP Orphan we have an appreciative style of communication on an equal footing. This concerns dialogue with the team and the executives as well as cooperation with our partners. The flat hierarchy creates a pleasant work environment, where committed staff members are able to pursue their creative and self-organised style of work.
"The team members attend to patients with warmth and empathy. I think that’s simply marvelous."
Could you describe a typical day at work?
I have no such thing as a typical day at work. Each new day brings a great deal of new aspects and everything is changing rapidly. I can prove my flexibility in these circumstances. We try to implement structures with the aid of digital tools.
What, in your opinion, is the factor that motivates the staff members at AOP Orphan?
Our greatest motivation is based on the corporate purpose of AOP Orphan, which is to help people with rare diseases. The team members attend to patients with warmth and empathy, which I deeply appreciate. Improving the lives of these patients is the principal motivating factor for all staff members.
"My daily work reflects the diversity of AOP Orphan."
What do you appreciate most about your work?
I like the fact that my work entails attending various meetings or conferences, where I have the opportunity to meet with stakeholders and colleagues to exchange consistent information. In my various tasks, I have adequate possibility to introduce my own ideas, and can take responsibility in the decision-making process.
What do you appreciate in your daily interactions with people?
We have a friendly work environment where respectful interaction between individuals is paramount. We also like to arrange after-work activities among colleagues.
"We approach many things “spontaneously” in the positive sense of the term – that’s possible only because of the dynamic environment at AOP Orphan."
What do you appreciate most in your daily interactions?
Generally we have interdisciplinary exchange between all departments, including the executive level. Something very unusual in a pharmaceutical enterprise is that we work in flat hierarchies – the doors always remain open for one and all.
"Our studies are more complex than for example diabetes or vaccine studies, since we ought to seek patients with rare diseases. Thus, the collaboration with doctors and specialized hospitals is of utmost importance."
WHO WE ARE, WHAT WE DO AND HOW WE WORK.
We create value by making smart decisions and taking action in a transforming and demanding environment. Change is a part of our business and therefore we are flexible and maintain a positive outlook to find the best solutions for the benefit of patients.
We are driven by the pioneer mindset of the company’s founder who aimed to make targeted treatment available to as many patients with rare diseases as possible. This ambition is the basis of our daily determination.
Effective communication and aligned decisions guide our actions. We are one strong international team working towards common, meaningful goals to achieve our mission.
We are responsible for our actions and take ownership for outcomes at all organizational levels. Living the principles of a learning culture and thinking beyond departmental boundaries helps us to accomplish ambitious goals. We always act with integrity .
Mag. Elisabeth Eriksson | International Brand Manager
We work with ambitious employees who continue to develop and grow. They make AOP Orphan successful and represent who we are – experts in our fields. Tailoring what we do to our patients’ needs is what drives us.
"My wish for the future is that we continue to make a valuable contribution to medical research in rare diseases, as it is our core competence."
"For more than 20 years AOP Orphan has been very successfully developing and providing therapies and care for patients with rare diseases and we are committed to do so in the future. Our strong pan-European market presence and our deep expertise in Research and Development forms the backbone for our future success. Through close contact and cooperation with the scientific community AOP Orphan is able to embed the latest results and findings in our research programs for the benefit of patients."
"It is our collective ambition at AOP Orphan not only to develop the new treatments but also to guarantee secure and efficient supply and care in all countries where we are present with own offices as well as in the markets covered by our partners. We feel responsible to giving hope, solution and relief to the patients with rare diseases.”