
Biotechnology • Pharmaceuticals
Tubulis GmbH is a biotechnology company specializing in the design and development of next-generation antibody–drug conjugates (ADCs) for cancer treatment. The company leverages proprietary platform technologies to generate uniquely matched ADCs with improved biophysical properties, durable on-tumor delivery, and strong preclinical anti-tumor activity. Its lead clinical programs, TUB-040 (anti-NaPi2b) and TUB-030 (anti-5T4), target high-need solid tumor indications, and Tubulis advances both its proprietary pipeline and partnered programs with the aim of expanding the therapeutic potential of ADCs for patients and collaborators.
51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
October 16
🗣️🇩🇪 German Required

Biotechnology • Pharmaceuticals
Tubulis GmbH is a biotechnology company specializing in the design and development of next-generation antibody–drug conjugates (ADCs) for cancer treatment. The company leverages proprietary platform technologies to generate uniquely matched ADCs with improved biophysical properties, durable on-tumor delivery, and strong preclinical anti-tumor activity. Its lead clinical programs, TUB-040 (anti-NaPi2b) and TUB-030 (anti-5T4), target high-need solid tumor indications, and Tubulis advances both its proprietary pipeline and partnered programs with the aim of expanding the therapeutic potential of ADCs for patients and collaborators.
51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
• Oversight and responsibility (review, assessment, and approval) for stability studies of critical reagents, ADC intermediates, drug substance, and drug product from all projects within Tubulis. • Support phase-appropriate analytical method qualification/validation at contract manufacturing organizations and support method transfer. • Interpretation of in-house analytical data, including result documentation/certification, for both internal and external material according to our platform. • Handling of changes, deviations, and OOX. • Contribute to specifications for intermediates, drug substance, and drug product. • Contribute to comparability studies.
• A degree in biotechnology, biochemistry, chemistry, or related subjects (B.Sc. or M.Sc.). • 3–5 years’ experience in a GMP area and related processes (stability testing, method qualification/validation, changes, investigations, etc.). • Experience in a biopharmaceutical laboratory. • Precision, analytical sense, and capability to work in a team. • Good proficiency in spoken and written English. • German spoken at B1 level. • Preferred Qualifications: ADC experience; linker payload experience.
• Impact that matters : Contribute to breakthrough therapies. • Global mindset : Work in an international, diverse team. • Grow & thrive : Develop your career in a supportive, fast-moving environment. • Innovation every day : Push boundaries with cutting-edge science.
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