Progress prospers with inspiration and curiosity. For 30 years Miltenyi Biotec has been developing products and services that are used in basic research, translational research and cell therapy. Today we are a team of more than 3,000 scientists, physicians, engineers, marketers and numerous other specialists. At Miltenyi Biotec, innovative ideas are being turned into cutting edge products. Together, we are passionate about driving biomedical progress towards curing severe diseases.
You and your team are responsible for Miltenyi’s pre-clinical in vivo You generate and establish new in vivo models in the areas of oncology and neurodegenerative diseases. In addition, you develop novel methods for tracking of cellular therapies.
You are planning, conducting and analyzing CAR or TCR modified immune cells, hematopoietic stem cells and pluripotent stem cell derived cells in in vivo studies followed by documentation for filing clinical trial applications at regulatory agencies.
You take responsibility for the strategic planning and establishment of clinically relevant cell tracking concepts.
Due to your close cooperation with other departments such as Clinical Development, RA, QA, and Marketing as well as with external cooperation partners and CROs you collect and provide all necessary information and communicate them to your team. In regular meetings you inform the MM Board about your progress.
Using your broad network, you establish and expand collaborative projects with academic groups and industry to fulfill Miltenyi’s approach to “Make cancer history” - be part of our team!
You have a PhD in biology, immunology, biomedicine, veterinarian or a similar field and have subsequently gained relevant scientific experience with focus on immunology research within an industry setting or a postdoc role.
In-depth professional experience in the field of in vivo studies, including liquid and solid tumor models and connected analysis methods (especially in vivo imaging) are essential. Ideally, you worked with patient derived xenograft models, humanized mouse models or models for Parkinson’s disease before.
A solid background in biometric study design and statistical analysis is required to fulfill the demands of this role, ideally you have gained experience in a GLP setting and documentation for IND filings.
You have gained substantial experience in leading a team and independently developing your field of expertise. You are familiar with resource management and have made use of your project management skills and reporting tools before.
You are enthusiastic about working with interdisciplinary topics. A conceptual and structured way of working as well as a high degree of commitment are part of your working style.
What we offer
A modern workplace and exciting opportunities in the development of technologies with a secure future
Cross-border intercultural cooperation and short communication channels
A collegial corporate culture and flexible working hours enable time management on your own terms
Personalized employee development program: specialist and personal training courses provided by our own training academy
Diverse corporate benefits with regard to employee health, sport, and staff events
If you have the skills and qualifications for this position, please use the link to send us your details (application letter, curriculum vitae, references and certificates). Please give us some idea of when you can start and the kind of salary you are looking for.