{"id":132345,"title":"Process Engineer Downstream Production (m/f/d)","company":"ProBioGen AG","city":"Berlin","region":"Berlin","location":"Berlin, Berlin","work_model":"unknown","employment_type":"full_time","employment":["full_time"],"roles":["software"],"visa":"not_mentioned","relocation":"not_mentioned","posted_at":"2026-09-08T00:00:00+00:00","tools":[],"seniority":"unknown","years_experience_min":null,"german_requirement":"required","german_level":"C1","english_requirement":"required","english_level":"unspecified","team_language":"unknown","confidence":0.7,"method":"rules","language_badge":"German required (C1)","language_evidence":"C1-level proficiency in spoken and written German and English","requirements_snippet":null,"url":"https://probiogen-portal.rexx-systems.com/Process-Engineer-Downstream-Production-mfd-eng-j500.html","source":"rexx","agency":null,"description_text":"Who we are\nProBioGen 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.\n\nThrough our research, we support the development of effective and safe medicines – for example, for the treatment of cancer and other serious diseases.\n\nAs 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.\n\nWe have been growing steadily since 1994 – become one of tomorrow’s innovation drivers and apply now!\nWhat you create\n• Large-scale GMP production: Independently planning, executing, and monitoring downstream processing steps such as filtration and chromatographic procedures (250–1,000 liters) under GMP conditions\n• Documentation and quality management: Creating and updating GMP-compliant documents, such as SOPs and batch record reviews\n• Process Transfer: Planning, coordinating, and documenting process transfers from development to production\n• Quality and Process Optimization: Ongoing review and optimization of processes to improve yield and efficiency\n• Ensuring Compliance: Ensuring compliance with regulatory requirements in accordance with GMP standards, as well as providing support during audits and inspections\nWhat you bring along\n• Bachelor’s or master’s degree in a science field such as biotechnology, bioprocess engineering, biochemistry, or a comparable field\n• Experience in a GMP production environment in the DSP field\n• In-depth knowledge of chromatography, filtration technologies, and virus inactivation is a plus\n• Experience in late-stage clinical or commercial biopharmaceutical manufacturing, including technology transfer, process validation, PPQ, or Manufacturing Science & Technology (MSAT), is desirable\n• Understanding of process robustness, control strategies, and lifecycle considerations is a plus\n• Excellent communication skills, intercultural competence, and a willingness to collaborate internationally\n• C1-level proficiency in spoken and written German and English\n• Strong organizational skills, ability to work well in a team, and a solution-oriented, self-directed work style\nWhat you can expect\nProSphere. Partnership environment, company events\nProBalance. Flexible workschedule and special vacation days\nProHealth. Yoga, Shiatsu, health days and discounted membership in the Urban Sports Club\nProCare. Technical equipment, laboratory clothing, monitor glasses, company pension plan\nProTaste. Cafeteria with Convini fridge, daily fresh lunch specials and free drinks\nProTalent. Onboarding with mentoring program, innovation days, further training opportunities\nWhom to ask\nEvery talent is welcome!\nApply now via our online form! Do you have any questions? I will be happy to help you.Every talent is welcome!\nApply now via our online form! Do you have any questions? I will be happy to help you.","responsibilities_text":null,"requirements_text":null,"status":"open","duplicate_of":null,"first_seen":"2026-11-04T14:07:43.607267+00:00","responsibilities_summary":null,"requirements_summary":null,"all_tools":[],"posting_language":"en","evidence":[{"language":"english","requirement":"required","quote":"C1-level proficiency in spoken and written German and English","source":"rules"},{"language":"german","requirement":"required","quote":"C1-level proficiency in spoken and written German and English","source":"rules"}],"years_experience_max":null,"mobility_evidence":[],"model_version":"rules-8","english_badge":"English required","company_id":17432}