Take on the role of Inspection Readiness Associate at OmniaBio in Hamilton, specializing in GMP compliance and quality assurance audits. Prepare the organization for regulatory challenges.

As a member of the Quality Compliance team at OmniaBio, you will be responsible for all facets of inspection readiness within a energetic GMP environment. Your role entails using quality metrics and regulatory intelligence to enhance operational preparedness. Collaborating with key stakeholders, you will help maintain the rigorous compliance necessary for client and regulatory audits.

Key Responsibilities:
• Maintain expertise in GMP related to gene therapy
• Organize and plan audits with business unit leaders
• Liaise between teams for effective audit preparation




• Ensure timely audit responses and commitment completion
• Host client and health authority audits as necessary

Requirements:
• Bachelor’s degree in science or engineering
• 5-10 years’ experience in GMP compliance
• Knowledge of compliance in sterile manufacture
• Proven ability to prepare and host audits
• Exceptional communication and presentation skills

Elevate your career in quality compliance with OmniaBio, leveraging your extensive expertise in Hamilton.
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📌 OmniaBio Quality Assurance Auditor (Ontario)
🏢 Centre for Commercialization of Regenerative Medicine
📍 Ontario