Manager, Manufacturing Operations

What you’d do

Manage day-to-day operation of a Drug Product Facility in a cGMP environment, directing staff and task assignments, authoring or approving batch documentation, and leading event investigations, CAPA and change controls. Full time. Found on the employer's careers page on Oct 17, 2026. Apply through the link.

You’ll need

• cGMP principles and practice in a pharmaceutical environment
• Process, equipment, and facility validation experience
• Staff management and task prioritization
• Event investigations, CAPA and change controls
• Strong interpersonal, communication and organizational skills