Bayer seeks an incumbent who possesses the following: Required Qualifications: Bachelor's degree in Biotechnology, Biology, Biochemistry, Chemical Engineering, or a related field; 4-6 years of cGMP biologics or cell therapy manufacturing experience with hands-on work in solution preparation, cell expansion/culture, and aseptic fill/finish; Proficiency with single-use technology systems, including setup, operation, and troubleshooting; Working knowledge of phase-appropriate cGMP practices and documentation from clinical through launch, including sampling, automation, batch records, and change control; Experience monitoring and controlling processes using data trending and/or statistical process control, with the ability to escalate issues and support investigations; Demonstrated ability to author, redline, and review controlled documents and SOPs for equipment and processes; Experience supporting deviations, conducting root cause analyses, and implementing effective CAPA to prevent recurrence; Familiarity with commissioning and qualification activities, including IOPQ and executing C&Q documentation under supervision; Strong cross-functional collaboration skills partnering with Development and MSAT to align on process, equipment, materials, and automation; Excellent oral, written, and presentation communication skills to ensure effective knowledge transfer across shifts and to leadership; Proven ability to create, own, and drive business processes of moderate complexity to achieve operational readiness; Demonstrated commitment to safety, including participation in safety investigations and regulatory/internal audits; Willingness to work across CT-MOD areas and shifts as business needs require. Preferred Qualifications: Master's degree in Biotechnology, Biology, Biochemistry, Chemical Engineering, or a related discipline; 6+ years of cGMP experience in cell therapy, gene therapy, or biologics manufacturing, including late-stage and launch products; Direct experience in a clinical cell therapy environment (e.g., autologous or allogeneic cell therapies) using single-use technologies; Hands-on experience with end-to-end cell therapy processes, including cell expansion, differentiation, and fill/finish for a single cell line or platform; Experience leading or acting as a subject matter expert in regulatory inspections and internal audits; Advanced experience with statistical process control tools and data analytics (e.g., JMP, Minitab, Spotfire, or similar); Demonstrated experience driving continuous improvement or operational excellence initiatives (e.g., Lean, Six Sigma, Kaizen); Prior experience mentoring or training operators or associates and developing training curricula or materials; Experience with electronic batch records (EBR), MES, and automation platforms commonly used in cell therapy manufacturing; Familiarity with commissioning, qualification, and validation (CQV) for cell therapy equipment and single-use systems.