Join OmniaBio in Hamilton, Ontario, as an Associate I in Quality Assurance and help ensure quality in cell and gene therapies. This role emphasizes manufacturing compliance and requires a motivated individual.

In your new position at OmniaBio, you will provide essential support within the Quality Assurance team. You’ll oversee GMP compliance through quality system management and assess manufacturing outputs. Collaborating across functions, you will ensure high standards of product quality and adherence to regulatory requirements.

Key Responsibilities:
• Ensure quality service delivery for cell therapy products
• Review batch records to confirm GMP compliance
• Collaborate on master batch record preparation
• Participate in internal and supplier audits as needed
• Manage documentation training programs for staff

Requirements:
• High school diploma with science coursework
• 1-2 years in a related GMP production role
• Familiarity with GMP regulations and QA practices
• Strong attention to detail and organizational skills
• Ability to adapt to a dynamic work workplace

Contribute to quality excellence and innovative therapies at OmniaBio.
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📌 Associate I in Quality Assurance Role (Ontario)
🏢 OmniaBio
📍 Ontario