Join Omnia Bio as an Inspection Readiness Associate to enhance your quality compliance career. Focus on preparing for regulatory inspections and ensuring client satisfaction.

This role at Omnia Bio in Hamilton, ON is key to maintaining the highest quality compliance standards in cell and gene therapy manufacturing. With responsibilities focused on managing audit readiness, you will ensure the organization is prepared for all inspections.

You will collaborate with business leaders and facilitate effective communication to drive compliance initiatives.

Key Responsibilities:

- Develop strategies for client and regulatory audits
- Coordinate with internal teams to sustain audit readiness
- Ensure compliance with current GMP standards
- Engage in continuous improvement initiatives
- Host and support external audits effectively

Requirements:

- Bachelor’s degree in a scientific or engineering discipline
- 5-10 years in a related industry role
- Proven knowledge of GMP regulations and compliance
- History of hosting client and regulatory audits
- Robust written and oral communication skills

Bring your expertise in quality compliance to Omnia Bio and help shape the future of biomanufacturing.

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📌 Inspection Readiness Expert in Hamilton (Canada)
🏢 Centre for Commercialization of Regenerative Medicine
📍 Canada