Bayer seeks an incumbent who possesses the following: Required Qualifications: Bachelor's degree in a relevant life science or engineering discipline (e.g., Biotechnology, Cell Biology, Biochemistry, Biomedical Engineering or related field); 5-7 years of relevant experience in cell therapy, biologics, or advanced therapy medicinal product (ATMP) manufacturing, including hands‑on experience with mammalian cell culture and aseptic processing in a cGMP environment; Demonstrated expertise in end‑to‑end cell culture operations such as solution preparation, cell expansion and differentiation, cell banking, and drug product filling and packaging, including experience with single‑use technologies (SUT); Strong understanding of cGMP regulations, quality systems, documentation practices, and compliance expectations for clinical and launch‑stage products; Proven experience supporting or leading new product introductions (NPIs) and/or technology transfers into manufacturing, working closely with development and MSAT or equivalent functions; Proficiency in using data analysis and, where applicable, statistical process control tools to monitor, troubleshoot and optimize manufacturing processes; Experience authoring, reviewing and approving controlled documents (e.g., SOPs, batch records, work instructions) and supporting equipment commissioning and qualification activities. Preferred Qualifications: Advanced degree (e.g., Master's or PhD) in a relevant scientific or engineering discipline; More than 7 years of experience in clinical or commercial cell therapy manufacturing, including exposure to late‑stage and launch activities; Experience designing and delivering technical training curricula and acting as SME trainer for manufacturing teams; Demonstrated ability to lead cross‑functional initiatives, influence stakeholders outside of manufacturing, and represent manufacturing in audits, investigations and project forums; Strong communication, collaboration and coaching skills, with the ability to work effectively in a fast‑paced, highly regulated, and multidisciplinary environment; Experience with automation, electronic systems (e.g., MES, LIMS, electronic batch records) and continuous improvement methodologies to drive process robustness and efficiency; Willingness and ability to work flexible hours, including modified shifts and occasional off‑hours or weekend work, to support time‑critical manufacturing and surgical schedules.