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
- Strong 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 in Oakville employer: Vital Bio
Vital Bio is an exceptional employer located in Oakville, Canada, offering a dynamic work environment where innovation thrives. As a Senior Mechanical Engineer, you will be part of a collaborative team dedicated to advancing robotic diagnostics systems, with ample opportunities for professional growth and development. The company fosters a culture of creativity and support, ensuring that employees are empowered to make meaningful contributions to the future of life-science instrumentation.
