OmniaBio Inc. is bringing life-saving cell and gene therapies to patients around the world.
Hamilton, Ontario
OmniaBio is redefining the future of cell therapy manufacturing through its proprietary AI-powered Intelligent Factory™. Purpose-built to accelerate discoveries and industrialize production, the Intelligent Factory™ integrates artificial intelligence and automation across the entire manufacturing lifecycle. With a focus on autologous CAR-T and other advanced therapies, OmniaBio’s platform enables scalable, efficient, and high-fidelity production by embedding predictive analytics, robotic bioprocessing, and digital quality systems into a unified, closed-loop system. This approach not only enhances throughput and consistency but also positions OmniaBio as a next-generation CDMO partner for innovators seeking to bring life-saving therapies to patients faster.
On-site · Hamilton
The Manufacturing Associate will execute production processes for cell and gene therapies while adhering to strict GMP guidelines and documentation standards. They are responsible for operating cleanroom equipment, maintaining a safe environment, and participating in continuous improvement and validation activities.
On-site · Hamilton
The Cleaning Technician I is responsible for cleaning and housekeeping activities within clean rooms, laboratories, and material storage areas. They must ensure all documentation is completed accurately according to GMP standards and support preventative maintenance programs.
On-site · Hamilton
Responsible for planning and coordinating work orders and preventive maintenance using the SAP PM module to support cGMP activities. The role manages facility vendors, inventory levels, and maintenance documentation to minimize business downtime.
On-site · Hamilton
The Maintenance Planner is responsible for coordinating work orders and preventive maintenance to support cGMP activities while managing the CMMS and inventory systems. They collaborate with functional teams to optimize schedules, manage vendor activities, and ensure regulatory compliance through accurate documentation and reporting.
On-site · Hamilton
The Cleaning Technician I performs cleaning and housekeeping duties in manufacturing and storage areas to ensure compliance with GMP standards. They also assist with preventative maintenance, documentation, and inventory monitoring for cleaning supplies.
On-site · Toronto
The role supports materials flow and maintains inventory accuracy to ensure production needs are met. Responsibilities include performing packouts, managing shipments, and utilizing SAP for supply chain activities within a GMP environment.
On-site · Toronto
The Supply Chain Technician supports material flow, inventory accuracy, and procurement processes within a GMP-regulated manufacturing facility. They are responsible for coordinating shipments, performing inventory reconciliations, and ensuring all supply chain activities adhere to company policies and safety standards.
On-site · Hamilton
The role supports materials flow and maintains inventory accuracy to ensure production needs are met. Key tasks include performing pharmaceutical packouts, managing shipments, and utilizing SAP for supply chain activities.
On-site · Hamilton
Support materials flow and maintain accurate inventories and supplies to ensure production of customer orders. Responsibilities include performing pharmaceutical packouts, managing shipments, and utilizing SAP for supply chain activities.
On-site · Hamilton
The Manufacturing Support Technician supports clean room manufacturing activities by facilitating material supply, waste removal, and environmental monitoring. This role ensures adherence to Good Manufacturing Practices and maintains cleanliness in production areas.
On-site · Hamilton
Coordinate inbound and outbound shipments of critical materials and final products while ensuring compliance with GMP and GDP standards. Manage procurement activities, supplier interactions, and ERP data accuracy to support cell and gene therapy manufacturing.
On-site · Hamilton
The Microbiologist is responsible for environmental monitoring, aseptic process simulation, and maintaining clean room conditions within a GMP manufacturing environment. They will manage sample testing, equipment qualification, and collaborate with production teams to ensure quality and compliance.
On-site · Hamilton
The Compliance Associate ensures departmental adherence to GMP standards by managing documentation, investigations, and quality metrics. They also lead cross-functional teams in risk assessments, CAPA plans, and regulatory audit preparations.
