Instrumentation Manufacturing Engineer - Medical Devices

Accelero; Trowbridge; On-site; GBP 45,000 - 70,000; Full time

Job summary

Accelero in the United Kingdom seeks a Manufacturing Engineer (Instrumentation) to design, implement, monitor and maintain manufacturing processes for medical device production. The role sits at the interface between design, quality and external manufacturing partners to ensure products can be built reliably, cost-effectively and at scale.

You will review processes, support verification and validation with contract manufacturers, maintain process documentation, and drive improvements in

Qualifications

• Experience in medical device manufacturing within regulated environments.
• Experience with manufacturing transfer, scale-up and collaboration with contract manufacturers.
• Experience maintaining documentation under ISO 13485.
• Min 5 years in a regulated industry with quality systems.

Responsibilities

• Review manufacturing processes and workflows for improvements with line operators, vendors and suppliers.
• Support verification and validation of production lines at contract manufacturers with appropriate test suites and in-line controls.
• Apply product design and assembly knowledge to manufacturing processes.
• Maintain process documentation (CAPA, BOMs, specifications) in line with QA requirements.
• Develop processes and procedures to meet production targets.
• Design systems and equipment to reduce time and cost while improving quality and safety.
• Collaborate with design engineers to optimize for manufacturability and assembly.
• Ensure reliable production of products and sub-assemblies.
• Manage projects using solid engineering principles.

Job description

Accelero in the United Kingdom seeks a Manufacturing Engineer (Instrumentation) to design, implement, monitor and maintain manufacturing processes for medical device production. The role sits at the interface between design, quality and external manufacturing partners to ensure products can be built reliably, cost-effectively and at scale.

You will review processes, support verification and validation with contract manufacturers, maintain process documentation, and drive improvements in