The Advisor is responsible for upstream process development activities related to producing bioproduct active pharmaceutical ingredients, including cell line development, cell culture process definition and optimization, process robustness studies, process transfers to pilot plants and manufacturing sites, and authorship of upstream process development sections of regulatory submissions. The role works closely with scientists in BR&D, Discovery, Technical Services for Manufacturing, and Manufacturing, and participates in multidisciplinary CMC project teams supporting bioproduct process and product development. The position includes designing and interpreting experiments, troubleshooting technical issues, contributing innovative ideas and technologies, supporting process transfers, and preparing technical reports and regulatory documents. The Advisor also works with external collaborators and supports departmental initiatives, external engagement, and process innovation across the portfolio. Work must comply with applicable Development Quality, Regulatory, HSE, GLP, and GMP requirements.
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Job Type
Full-time
Career Level
Senior
Education Level
Ph.D. or professional degree