Description

You will lead and oversee GMP manufacturing operations on the 2nd shift, ensuring safety, aseptic practices, and compliance while training team members and driving continuous improvement.

Requirements

• Prior leadership experience in GMP manufacturing facility
• Hands-on experience in writing and reviewing documentation
• Experience in bio-manufacturing unit operations
• Good writing and oral communication skills
• Ability to adhere to regulatory policies and procedures

Responsibilities

• Supervise, train, and mentor upstream, downstream, drug product, and banking teams
• Oversee routine and critical manufacturing operations
• Ensure documentation meets good documentation practices
• Coordinate daily scheduling and staffing
• Act as primary contact for troubleshooting and issue resolution