Computer scientist

Get started now as a Junior Information Scientist (m/f/d)

We are currently looking for a Junior Information Scientist (m/f/d) on behalf of our business partner from the pharmaceutical industry in Biberach .

Apply today and start your new job tomorrow We welcome applications from people with disabilities.

Here's what we offer

Attractive salary and long-term job security through group affiliation Up to 30 days vacation per year Contribution to company pension scheme after end of probationary period Extensive social benefits, including Christmas and vacation bonuses Reimbursement of travel expenses As a rule, a permanent employment contract Good chances of being taken on by our business partners Tailored further training 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 to achieve common goals and take on the responsible role of sub-project manager.

- You will also be responsible for the support and further development of complex IT systems in the (non-) GMP environment.

- This includes error analysis, system adjustments, the implementation of functional tests and subsequent documentation.

- In addition, you will be responsible for evaluating and establishing new innovative IT solutions in close cooperation with the users of the "Pharmaceutical Development" department.

- As a process expert, you will act as a link between the specialist department, the IT experts and external partners.

- Supporting the scientists in analyzing complex data rounds off your new area of responsibility.

Your profile

- Completed Master's degree in computer science, completed Bachelor's degree in computer science with at least 2 years of professional experience or a comparable qualification

- Several years of experience with the computer systems Signant Health SmartSignal Supplies - GxP Inventory, Loftware Prisym360, Körber PAS-X, SAP modules PPI, MM, (E)WM

- Initial experience with Computerized System Validation and the associated regulations such as GxP, 21 CFR Part 11 and ISPE GAMP 5 & Cloud Administration

- Initial experience in the field of pharmaceutical process knowledge in the areas of formulation development, process development, GMP production of clinical trial samples and their distribution

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

- Strong team player with the ability to work in an agile and focused manner in cross-functional teams

- Social, communicative and methodical skills in combination with a structured, goal-oriented and independent way of working

- Ability to analyze and transfer complex interrelationships

- Very good written and spoken German and English language skills

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