We are seeking a highly skilled and detail-oriented professional to manage and execute operations in sterile injectable manufacturing. The role involves handling vial washing, depyrogenation, aseptic filling, autoclaving, lyophilization (lyo), compounding, and microbiological quality control activities within a regulated pharmaceutical environment. The candidate must ensure compliance with cGMP, regulatory standards, and aseptic practices.

Key Responsibilities

A. Production – Aseptic Area Operations