Join a global biopharmaceutical company advancing innovative therapies in oncology and rare diseases. With a strong pipeline and a collaborative, science-driven culture, this organization empowers its leaders to shape the future of biologics manufacturing. We are seeking a strategic and hands-on leader to drive the technology transfer of drug substance manufacturing processes, with a strong focus on Antibody-Drug Conjugates (ADCs). This role is critical in ensuring seamless scale-up and commercialization of complex biologics across internal and external manufacturing sites. Key Responsibilities Lead cross-functional site launch teams for DS manufacturing (clinical and commercial) Oversee tech transfer, PPQ, and validation activities in line with global CMC strategy Act as the technical interface between development, manufacturing, QA, and regulatory teams Evaluate CDMOs for clinical and commercial manufacturing, support facility fit assessments Contribute to regulatory submissions (IND, IMPD, BLA, NDA) and inspection readiness Recommend and implement new technologies to improve DS manufacturing performance Support data-driven decision-making and digitalization of tech transfer processes Your Profile PhD or equivalent in biochemistry, biotechnology, or related field 8 years in biopharma with deep experience in drug substance tech transfer and CMC Strong knowledge of GMP, regulatory frameworks, and biologics manufacturing Experience with ADCs or other complex biologics is highly desirable Proven leadership in cross-functional and global environments What's in it? High-impact role in a global matrix organization Work on cutting-edge biologics with real-world patient impact Hybrid flexibility and international collaboration Opportunity to shape the future of ADC manufacturing Die Personalberatung SThree betreut die ausgeschriebene Stelle im Auftrag ihres Kunden.