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
Support clean room manufacturing by facilitating material supply, waste removal, and environmental monitoring. Maintain the cleanliness and safety of production support areas while adhering to GMP and documentation standards.
On-site · Hamilton
The role is responsible for managing all aspects of inspection readiness, including planning and hosting client and regulatory audits. It involves collaborating with SMEs and business leaders to ensure GMP compliance and timely completion of audit commitments.
On-site · Hamilton
Support materials flow and maintain accurate inventory control to ensure production needs are met.SSSCSSSB. Responsibilities include managing pharmaceutical packouts, coordinating shipments, and utilizing SAP for supply chain activities.
On-site · Hamilton
Provides comprehensive administrative and operational support to the Site Head and leadership team, including complex calendar management and meeting coordination. Manages onsite logistics for visitors, clients, and employee engagement activities to ensure smooth daily site operations.
On-site · Hamilton
The Inspection Readiness Associate is responsible for preparing the organization for client audits and regulatory inspections through quality metrics and internal audits. They will liaise with internal teams and external stakeholders to ensure compliance standards are maintained and audit commitments are met.
On-site · Hamilton
The Administrative Coordinator provides onsite operational and executive support to the Site Head and leadership team, including calendar management and meeting coordination. They also manage visitor logistics, office services, and employee engagement initiatives to ensure smooth daily site operations.
On-site · Hamilton
The role focuses on delivering quality assurance services for cell and viral product manufacturing, including product release and batch record review. It involves managing quality systems such as deviations, CAPAs, and change controls while ensuring GMP compliance across the organization.
On-site · Hamilton
The Associate I, Quality Assurance, is responsible for managing GMP quality systems, including batch record review, documentation control, and providing on-the-floor support for manufacturing teams. They will also participate in internal and supplier audits while collaborating with cross-functional teams to ensure compliance and continuous improvement.
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 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
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
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 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.
