Become an Inspection Readiness Associate in Hamilton, ON with OmniaBio, specializing in quality compliance for audits and inspections. Drive engagement in regulatory processes while ensuring compliance.

In this role, you will be vital to OmniaBio’s Quality Compliance team, establishing readiness for client and regulatory inspections. With 5-10 years of relevant industry experience, your expertise in GMP compliance will be essential. Responsibilities include planning audits, liaising with business leaders, and hosting inspections, alongside maintaining comprehensive knowledge of evolving regulations.

Key Responsibilities:
• Plan and prepare for all audits and inspections
• Organize subject matter experts for audit support
• Liaise with business units to ensure audit readiness




• Host health authority and client audits as needed
• Maintain an up-to-date understanding of GMP standards

Requirements:
• Bachelor’s degree in science or engineering
• 5-10 years of industry experience in cell and gene therapies
• Knowledge of GMP regulations and quality assurance principles
• Experience managing audit responses and commitments
• Solid presentation and communication skills

Utilize your skills in GMP compliance and audit preparedness to elevate OmniaBio’s mission in Hamilton.
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📌 Quality Compliance Specialist at OmniaBio (Ontario)
🏢 Centre for Commercialization of Regenerative Medicine
📍 Ontario