For 35 years, we have been developing cutting-edge science and technology to empower biomedical research and personalized medicine. We combine excellence from more than 60 disciplines in natural sciences, engineering, and informatics to make a significant contribution to biomedical sciences. We encourage a creative working environment driven by pioneering spirit – to seek new horizons – boldly envisioning the future and turning it into reality. Today, more than 4,700 experts from over 50 countries contribute to our sustainable success.
Job Description
* In this exciting role you join a motivated team focused on developing the next generation CliniMACS Prodigy® T cell application for clinical use.
* You will coordinate the development and market release of the CliniMACS Prodigy® system which includes novel solutions for the automated and completely closed production of genetically modified T cells from the cellular starting material to the final drug product (end-to-end process) as well as the implementation tools for improved robustness and usability.
* This requires close collaboration with multidisciplinary teams across Miltenyi Biotec's departments.
* You will be responsible for preparing, summarizing and reporting results in accordance with clinically relevant guidelines for ATMP manufacturing.
* You will coordinate a small team, that will be trained on CliniMACS Prodigy® using your experience and knowledge in system and process development.
Qualifications
* You have a MSc or PhD in Life Sciences, ideally with initial professional experience in clinically relevant process and system development.
* You convince us with a broad expertise in immunological techniques such as cultivation, activation and gene modification of human T cells and in vitro functional analysis.
* You are familiar with the GMP production of genetically modified T cells and also have a sound understanding of T cell-specific processes, ideally on CliniMACS Prodigy®.
* You also have experience in project management and project leadership. Practical knowledge in the field of quality assurance and regulatory affairs as well as experience in documentation with and under design control according to DIN EN ISO 13485 are an advantage.
* As a committed and reliable person, you enjoy working in a team and have good organizational and networking skills. Quality awareness is a matter of course for you.
Additional Information
What we offer
* An exciting project in the field of adoptive T cell therapies.
* Diversity: International teams and cross-border intercultural communication
* Room for creativity: It’s the most clever solution that we always strive for
* Health & Sport: We offer a wide range of corporate sports activities and health provision
* Miltenyi University: A clever mind never stops learning, take advantage of our inhouse Training Academy
We are looking forward to your application
You have the skills and
qualifications
required for this position, please use the link to send us your documents (cover letter, resume, references and certificates).
Please give us an idea of when you could start and what your salary expectations are.