Shape the future of drug development with us!
In a dynamic and international environment, we bridge the gap between cutting-edge IT and pioneering science. We are seeking a dedicated individual to join our interdisciplinary team. This individual will manage complex IT systems in (non-)GMP environments, establish innovative digital tools, and act as a strategic liaison to elevate our processes to the next level. If you are passionate about combining data analysis with project management skills to make a real contribution to the future of healthcare, become part of our success story as a Junior Information Scientist (m/f/d).
Here's what we offer
1. Attractive salary and long-term job security through affiliation with a large corporation.
2. Up to 30 days of vacation per year
3. Company pension scheme contribution after the end of the probationary period
4. Extensive social benefits, including Christmas and holiday pay
5. Reimbursement of travel expenses
6. Usually an open-ended employment contract
7. Good opportunities for acquisition with our business partners
8. Tailored professional development opportunities and free language courses
9. A wide range of employee benefits
Your tasks
10. In your new role, you will work in international, interdisciplinary project teams and assume responsibility as a sub-project manager to achieve common goals.
11. They maintain and further develop complex IT systems in (non-)GMP environments, including error analysis, system adjustments, functional tests and documentation.
12. They evaluate and establish innovative digital solutions in close coordination with users, including modern approaches to software development and the use of AI tools.
13. As a process expert, you act as an interface between specialist departments, IT experts and external partners, driving continuous improvement.
14. In addition, you will support scientists in analyzing complex data, thus making an important contribution to well-founded drug development decisions.
Your profile
15. Completed Master's degree in Computer Science, alternatively a completed Bachelor's degree in Computer Science with several years of professional experience or a comparable qualification with relevant professional experience
16. Proven experience with data structures, techniques for statistical data analysis, and expertise in current programming languages such as Python and R.
17. Prior experience in pharmaceutical process knowledge, particularly in formulation development, process development, and GMP-compliant manufacturing and distribution of clinical trial samples, is advantageous.
18. Strong teamwork skills and the ability to work agilely and in a goal-oriented manner in cross-functional teams.
19. High social, communicative and methodological competence, combined with a structured, independent and solution-oriented work style.
20. Excellent written and spoken German and English skills, due to close collaboration with national and international partners.
21. Willingness to be regularly present on-site and to work closely with the team; working from home is possible after consultation.