Process Development

This role provides technical leadership and hands-on support for sterile manufacturing operations, including Blow Fill Seal, prefilled syringe filling, and aseptic processing. It serves as a technical bridge between Manufacturing, QA, QC Microbiology, Engineering, and other departments to ensure sterile processes are scientifically sound, validated, and compliant. The position involves leading validation lifecycle activities, managing deviations and investigations, and improving control strategies for sterile assurance.