Advance your career with OmniaBio in Hamilton, Ontario, as an Associate I in Quality Assurance. You will play a vital role in ensuring compliance in cell and gene therapy manufacturing.

As Associate I, Quality Assurance, you will be involved in all aspects of GMP for cell and gene therapy products. Your work will encompass quality system management and provide support to manufacturing teams. This role demands flexibility and teamwork to maintain high quality and efficiency in production.

Key Responsibilities:
• Deliver quality services and assist in product release processes
• Prepare and amend master batch records and specifications
• Support on-the-floor compliance inspections and audits
• Manage documentation and training programs effectively
• Conduct audits and assist with regulatory compliance checks

Requirements:
• High school diploma along with relevant college courses
• 1-2 years of GMP production experience
• Understanding of applicable QA principles
• Excellent analytical and multitasking skills
• Comfortable in a agile and evolving workplace

Join OmniaBio to drive quality assurance in life-changing therapies.
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📌 Quality Assurance Associate I Position (Ontario)
🏢 OmniaBio
📍 Ontario