Daiichi Sankyo Europe GmbH | Germany | 85xxx Pfaffenhofen an der Ilm | Permanent position | Full time | Published since: 04.11.2026 on stepstone.de
Biologics Project Expert (m/f/d) Quality Control
At Daiichi Sankyo we are united behind a single goal: to improve life around the world through innovative medicines. With active innovation since 1899, presence in more than 30 countries and over 19,000 employees, we develop groundbreaking therapies in oncology, cardiovascular diseases, rare diseases and immune diseases. In line with our vision 2030, "to be an innovative global healthcare company that contributes to the sustainable development of society," we create a healthier, hopeful future for patients, their families and society. For our location in Pfaffenhofen we will now Biologics Project Expert (m/f/d)
* After clicking the Read more button, the original advert will open on our partner's website, where you can see the details of this vacancy and contact information. If you need a translation of this text, after returning to our website it will be prepared and you can read it by clicking the Show full translation button.
Your tasks • Your profile • What we offer
Planning, implementation and management of projects within quality control and implementation of new processes in bioanalytics Support in the optimization, digitization and automation of processes Support for laboratory management in technical and organizational issues Responsibility for the timely and GMP-compliant processing of deviations, CAPAs and change processes Development, validation, documentation and testing of analytical methods and analytical results Creation, updating and further development of standard work instructions (SOPs) to ensure efficient and GMP-compliant laboratory operation Active participation in internal self-inspections and external customer audits to ensure high quality standards Professional support and support for employees in the field of bioanalytics
Successfully completed study of biochemistry, pharmacy or comparable scientific studies Multiannual professional experience in the GMP-regulated pharmaceutical industry, ideally in the field of quality control Proven IT expertise and high affinity for digital systems, data management and process automation Long-term experience in the planning, implementation and documentation of qualification and validation activities Knowledge of bioanalytics and pharmaceutical analysis Wide cross-disciplinary know-how with deeper knowledge in quality management or GMP environment Very good knowledge of current pharmaceutical guidelines and legal requirements Structured, meticulous and goal-oriented working with decision-making strength, sense of responsibility and high quality standards
Attractive Benefits Work-life balance Personal growth and development Health and well-being
Location
![]() | Daiichi Sankyo Europe GmbH | |
| 85276 Pfaffenhofen an der Ilm | ||
| Germany |
The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.
For more information read the original ad