Associate Scientist II

Role: Technical lead for downstream GMP manufacturing processes in biopharma production, focusing on late-stage and commercial scale. Responsibilities: author validation protocols and reports, support process qualification and continuous verification, collect and analyze process data, troubleshoot technical challenges, and support process improvements and scale-up activities; collaborate with cross-functional teams and manage client relationships. Requirements: Bachelor's degree with 3+ years or Master's degree in relevant field; strong knowledge of GMP manufacturing, process validation, and data analysis. High-Value: GMP manufacturing, process validation, process improvements, technical transfers, biotech/biopharma production. WorkSetup: not specified.