Job Description
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
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