ProBioGen is an international biotechnology company based in Berlin-Weißensee, specialising in the development and manufacture of biopharmaceuticals and vaccines. Every day, 300 employees contribute through their creative and meticulous work to advance new therapies and establish innovations worldwide.
Through our research, we support the development of effective and safe medicines – for example, for the treatment of cancer and other serious diseases.
As a partner in the Berlin Center for Gene and Cell Therapies (BC GCT), we are also actively shaping the future of gene and cell therapies and the expansion of state-of-the-art GMP production facilities in Berlin.
We have been growing steadily since 1994 – become one of tomorrow's innovation drivers and apply now!
- Documentation tasks in the production environment:
- Preparation, review and approval of qualification documents for production equipment
- Conducting and documenting risk analyses at equipment level
- Initiating, processing and reviewing compliance activities such as non-conformities, CAPAs and CCOs
- Equipment qualification: You will help to maintain the qualification status of equipment and ensure that our systems are ready for operation
- Optimising processes: You will contribute to the creation and updating of SOPs to make our processes even more efficient and safe
- Large-scale production: Independently carrying out filtration and chromatographic processes (250–1,000 litres) under GMP conditions
- Cooperation between development and production: You will support process transfer and work closely with interdisciplinary teams to ensure new processes are implemented safely and efficiently
- GMP-compliant manufacturing: You will be part of the manufacturing of biological active substances and ensure that every batch meets regulatory requirements
- Completed training as a BTA, CTA, MTA or laboratory technician (m/f/d), a Bachelor's degree or equivalent qualification
- Experience with downstream processing, filtration and the purification of biological active substances is desirable
- Initial practical experience in the (bio-)pharmaceutical sector is an advantage
- Knowledge of GMP guidelines is an advantage
- Basic knowledge of CAPA and CCO processes, as well as risk analysis, is an advantage
- Flexibility, a sense of responsibility and a reliable, meticulous approach to work
- German at C1 level and English at B2 level, both spoken and written
- A solution-oriented, innovative and collaborative approach to work
ProSphere. Partnership environment, company events
ProBalance. Flexible workschedule and special vacation days
ProHealth. Yoga, Shiatsu, health days and discounted membership in the Urban Sports Club
ProCare. Technical equipment, laboratory clothing, monitor glasses, company pension plan
ProTaste. Cafeteria with Convini fridge, daily fresh lunch specials and free drinks
ProTalent. Onboarding with mentoring program, innovation days, further training opportunities
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