Advance your career with OmniaBio in Hamilton, Ontario, as an Associate I in Quality Assurance. You will play a vital role in ensuring compliance in cell and gene therapy manufacturing.As Associate I, Quality Assurance, you will be involved in all aspects of GMP for cell and gene therapy products. Your work will encompass quality system management and provide support to manufacturing teams. This role demands flexibility and teamwork to maintain high quality and efficiency in production.Key Responsibilities:Deliver quality services and assist in product release processesPrepare and amend master batch records and specificationsSupport on-the-floor compliance inspections and auditsManage documentation and training programs effectivelyConduct audits and assist with regulatory compliance checksRequirements:High school diploma along with relevant college courses1-2 years of GMP production experienceUnderstanding of applicable QA principlesExcellent analytical and multitasking skillsComfortable in a agile and evolving workplaceJoin OmniaBio to drive quality assurance in life-changing therapies.

📌 Quality Assurance Associate I Position (Hamilton)
🏢 OmniaBio
📍 Hamilton