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 Director of Business Development will execute the company's growth strategy by identifying prospective clients and negotiating manufacturing agreements. They will lead cross-functional teams to develop tailored proposals and manage ongoing client relationships to ensure revenue objectives are met.
On-site · Hamilton
The Manufacturing Associate II executes production processes for cell and gene therapies while adhering to GMP standards and documentation practices. They are responsible for operating clean room equipment, maintaining safety standards, and participating in root cause investigations.
On-site · Hamilton
The Manufacturing Associate will execute production activities for cell and gene therapies while adhering to Good Manufacturing Practices (GMP). They are responsible for operating cleanroom equipment, maintaining documentation, and supporting equipment qualification and validation processes.
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 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 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 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 · 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 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.
