Operations Specialist

Operations Specialist

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.

Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.

Role Overview

This position will be responsible for providing operational support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will partner with Technical Operations in support of personalized cell therapy production through safe and compliant manufacturing operations according to cGMP requirements. The individual will be responsible for driving and implementing a wide variety of improvements, ensuring alignment in support of the overall objectives and priorities of the plant. The role will require communication, coordination and collaboration across relevant cross functional groups to enable robust production, testing and release of product to patients.

Key Responsibilities

• Provides general support to all Operating Areas, e.g. Manufacturing, Warehouse, Logistics, Support Labs.
• Collaborates with Technical Operations who are responsible to provide process knowledge and expertise in support of GMP investigations, change controls, document control, process improvement, process validation and data management.
• Partners with Operational Excellence to implement improvements.
• Writes, reviews, owns and updates SOPs.
• Owns, provides assessments and takes actions in support of change controls.
• Owns CAPAs and associated project plans.
• Supports events such as Root Cause Analysis (RCAs) and FMEAs.
• Participates in kaizens and other project initiatives.
• Supports any business improvement efforts.
• Supports permanent inspection readiness and actively supports internal audits and regulatory inspections.
• Provides input to studies related to process improvement and implementation of new manufacturing technologies and associated protocols.
• Provides input and supports improvements related to the aseptic environment and technique.
• Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals.
• Distance visual acuity of at least 20 / 40 (Snellen) in both eyes without corrective lenses or visual acuity corrected to 20 / 40 (Snellen) or better with corrective lenses.
• Color Perception both eyes 5 slides out of 8.

Requirements