Start your career in Quality Assurance with OmniaBio in Hamilton, Ontario. As an Associate I, you will support Good Manufacturing Practices in cell and gene therapy while ensuring compliance across operations.
As Associate I, Quality Assurance, you will contribute to GMP manufacturing for transformative products at OmniaBio. The role focuses on manufacturing quality, quality systems, and outsourced activities. You will collaborate closely with various teams, providing in-suite support and ensuring compliance in production processes.
Key Responsibilities:
• Deliver quality services including product release for clients
• Prepare and review master batch documentation and specifications
• Support on-the-floor manufacturing teams for compliance
• Manage deviations, corrective actions, and quality systems
• Participate in internal audits and regulatory inspections
Requirements:
• High school diploma and additional science courses
• 1-2 years experience in GMP production support
• Understanding of GMP regulations and QA principles
• Detail-oriented with robust analytical skills
• Flexibility to adapt in a developing organization
Elevate your career in Quality Assurance and contribute to groundbreaking therapies with OmniaBio!
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