Bayer seeks an incumbent who possesses the following: Required Qualifications: Bachelor's degree in a science‑related field, preferably biology, cell/cellular biology, biochemistry, biophysics, computer science or a related discipline; Aseptic Processing Experience (ISO 5 or better) and cGMP experience; Strong understanding of data integrity, regulatory requirements (e.g., FDA, EMA), and cGMP requirements for pharmaceutical manufacturing; Ability to understand equipment functionality and independently troubleshoot and resolve equipment and process‑related issues; Excellent computer skills, including proficiency with Microsoft Office (Word, Excel, PowerPoint, Access) and experience with automation systems; familiarity with filling and isolator equipment; Ability to work on and communicate complex problems where analysis of situations or data requires evaluation of multiple factors, with effective written and verbal communication, networking, and presentation skills across shifts and functions; Proven ability to lead and work in teams, build sustainable cross‑functional partnerships, and influence, recommend, and help implement strategies, processes, and procedures; Willingness and ability to change shift schedules based on business and process needs, including providing off‑hour (night/weekend) coverage on short notice, and ability to lift up to 45 lbs in line with occupational/physical requirements. As a Production Specialist III Cell Therapy Drug Product, you are a key contributor within the Cell Therapy Module (CT‑MOD), responsible for clinical manufacturing of novel cell therapy drug substance from cell expansion through differentiation, fill/finish, and freezing using single‑use technologies; You collaborate closely with Biological Development (BD) and Manufacturing Science and Technology (MSAT) to introduce new products, ensure platform alignment, and support the development and implementation of CT‑MOD's business strategy; In this role, you work across multiple phases of the product life cycle-from clinical through launch-acting as a subject matter expert in at least one area while helping to shape robust, compliant, and innovative cell therapy manufacturing operations.