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.

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