Operations Supervisor

Legend Biotech is seeking an Operations Supervisor to join their Technical Operations team in Raritan, NJ. This role involves directing the daily production of personalized cell therapy in a cGMP environment.

Responsibilities:

• Lead and supervise multiple units within CAR-T process operations.
• Lead daily start of shift and wrap-up production meetings.
• Provide guidance and perform production tasks on the production floor.
• Support manufacturing investigations and create/revise operational procedures.
• Oversee the development of production personnel.
• Build partnerships with Manufacturing, Engineering, and Quality teams.
• Support the development of manufacturing processes and participate in department projects.

Requirements:

• Bachelor’s degree in Science, Engineering, or related field or equivalent experience.
• Minimum of 6 years of operations experience within a cGMP environment in the biotech/biopharma industry.
• Prior experience in manufacturing, quality, or engineering.
• Excellent communication and organizational skills.
• Proficiency with Microsoft Office tools.
• Availability to work in a day shift (1st or 2nd shift).
• Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell-based products.
• Strong leadership skills and ability to influence Operations associates.
• Ability to work independently and manage multiple tasks simultaneously.
• Strong analytical, problem-solving, and critical thinking skills.
• Ability to build strong partnerships and integrate with external collaborators.
• Clear verbal and written communication skills.
• Ability to lift a minimum of 25 lbs. and stand for a long period of time.

The role offers:

• Opportunity to work in a cGMP environment.
• Chance to contribute to the development of cell therapy Technical Operations.
• Be part of a cross-functional team.