Junior information scientist (m/f/d)

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

• Attractive salary and long-term job security through affiliation with a large corporation.

• Up to 30 days of vacation per year

• Company pension scheme contribution after the end of the probationary period

• Extensive social benefits, including Christmas and holiday pay

• Reimbursement of travel expenses

• Usually an open-ended employment contract

• Good opportunities for acquisition with our business partners

• Tailored professional development opportunities and free language courses

• A wide range of employee benefits

Your tasks

• In your new role, you will work in international, interdisciplinary project teams and assume responsibility as a sub-project manager to achieve common goals.

• They maintain and further develop complex IT systems in (non-)GMP environments, including error analysis, system adjustments, functional tests and documentation.

• They evaluate and establish innovative digital solutions in close coordination with users, including modern approaches to software development and the use of AI tools.

• As a process expert , you act as an interface between specialist departments, IT experts and external partners, driving continuous improvement.

• In addition, you will support scientists in analyzing complex data, thus making an important contribution to well-founded drug development decisions.

Your profile

• 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

• Proven experience with data structures, techniques for statistical data analysis, and expertise in current programming languages ​​such as Python and R.

• Prior experience in pharmaceutical process knowledge, particularly in formulation development, process development, and GMP-compliant manufacturing and distribution of clinical trial samples , is advantageous.

• Strong teamwork skills and the ability to work agilely and in a goal-oriented manner in cross-functional teams.

• High social, communicative and methodological competence, combined with a structured, independent and solution-oriented work style.

• Excellent written and spoken German and English skills , due to close collaboration with national and international partners.

• Willingness to be regularly present on-site and to work closely with the team; working from home is possible after consultation.