OmniaBio Quality Assurance Auditor
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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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