Process Engineer I

Role: Manufacturing Process Engineer responsible for supporting process development, validation, and optimization in biopharma manufacturing settings. Responsibilities: collaborate cross-functionally with EHS, quality, regulatory, and operations teams to address process challenges, execute validations (IQ/OQ/PQ/TMV), conduct statistical analyses for process improvement, investigate non-conformances, and implement lean six-sigma methodologies to enhance yields, reduce scrap, and ensure cost efficiency. Develop training programs, monitor KPIs, and participate in cross-departmental projects for process and product improvement. Qualifications: Bachelor’s degree in engineering or related field; 0-2 years of experience; proficiency in MS Office; knowledge of statistical process control tools (e.g., SPC, Minitab); desired lean six-sigma experience; strong communication and organizational skills; project management acumen preferred. High-Value: Entry-level to early-career role supporting manufacturing process improvements in biopharma, with focus on process validation, quality, and efficiency. Work setup: Not specified, likely on-site given manufacturing context.