Who we are
ProBioGen is an internationally operating biotech company based in Berlin-Weißensee, which has specialized in the development and production of biopharmaceutical active ingredients and vaccines throughout many years of experience. Every day, more than 300 employees contribute with their creative and diligent work to the establishment of new therapeutic developments in medicine and groundbreaking innovations worldwide.
Through our research, we support the development of effective and safe medical agents to help improve the cures for diseases such as cancer.
We have been growing steadily since 1994 - become an innovator of tomorrow and apply now!
What you create
• Execution of Analytical Procedures: Application of wet chemical, instrumental, and bioanalytical methods for process-related controls, release, and stability testing according to testing instructions.
• Material Analysis & Goods Receipt Control: Analysis and characterization of product developments, reference standards, as well as goods receipt control of raw and consumable materials.
• Method Development & Qualification: Conducting experiments for the development, qualification, and optimization of analytical methods, including troubleshooting.
• Documentation & Data Evaluation: GMP-compliant documentation of all tests and evaluation of results according to established specifications.
• Sample Management & External Shipping: Management of reference and stability samples and organization of sample shipments to external laboratories.
• Equipment Maintenance & Functional Assurance: Ensuring the operational readiness of laboratory equipment through maintenance, qualification, and repairs.
• Regulatory Support & QC Management: Support in compliance-related topics, change management, and ensuring GMP-compliant laboratory operations.
What you bring along
• Educational Qualification: Training as a (biological or chemical) laboratory technician, biological or chemical laboratory assistant, or a Bachelor's/Master's degree in a natural science field.
• Professional Experience:
o At least 3 years of professional experience in a regulated environment (GMP/ISO) required.
o Several years of professional experience in QC / goods receipt inspections preferred.
• Expertise: Experience with analytical methods in the biopharmaceutical field and in performing pharmacopoeial methods (Ph. Eur. / USP).
• Technical & Organizational Skills: Excellent IT skills and a high degree of responsibility and commitment.
• Language Skills: Proficiency in English sufficient to understand work instructions and testing guidelines.
What you can expect
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
