Lead cGMP technology transfer and process development for diagnostic assemblies at Vital Bio in an onsite manufacturing engineering role.
As a Manufacturing Engineer I, you will transfer products from engineering and assay development into manufacturing. You will design assembly processes for reagents and molded plastic components. The work spans prototypes, scale-up, and steady-state production. You will support repeatable, cost-effective, high-quality assemblies while applying lean principles, validation, and risk mitigation.
Key Responsibilities: Execute manufacturing process and technology transfers into cGMP production
Design assembly processes and define development activities
Assess manufacturing risks and develop effective mitigations
Lead equipment, facility,



and process validation protocols
Drive root cause analysis and continuous process improvement
Requirements: Bachelor’s degree in STEM
5+ years manufacturing engineering or operational experience
Experience with diagnostics, biologicals, reagents, and molded components
Familiarity with IVD validation, qualification, and cGMP processes
Robust analytical, communication, organizational, and collaboration skills
Apply manufacturing engineering expertise in cGMP technology transfer, validation, and continuous improvement for Vital Bio diagnostics.

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📌 Manufacturing Engineer cGMP Tech Transfer (Ontario)
🏢 Vital Bio
📍 Ontario