Graduate Production Quality Engineer: Build & Verify

Xstrahl, Inc; Brownhills; Vor Ort; GBP 26.000 - 38.000; Vollzeit

Zusammenfassung

Xstrahl, Brownhills, UK, is seeking a Graduate Production Quality Engineer to join the on-site production team. You will develop and maintain build manuals and work instructions, perform sign-off checks, and manage NCRs, CRs and related quality records to ensure traceability and compliance.

Working alongside experienced engineers on the shop floor, you will gain hands-on experience documenting processes, testing instructions, and supporting a regulated medical device environment, with

Qualifikationen

• A degree in engineering or related science subject.
• Clear written communication — able to turn a technical process into simple, step-by-step instructions.
• Organised with good attention to detail and accurate records.
• Practical and hands-on, keen to learn how systems are built.
• Willing to take ownership and see tasks through to completion.
• Comfortable using Microsoft Office.

Aufgaben

• Create and maintain build manuals for each Xstrahl system.
• Write clear, step-by-step work instructions for each build stage, with photos/diagrams.
• Capture build knowledge from experienced engineers for documentation and sharing.
• Test draft work instructions by having an engineer build from them and update them based on feedback.
• Keep build documentation under document control per Quality Management System.
• Support documentation for new products transferring into production.

Kenntnisse

Technical writing

Attention to detail

Hands-on

Problem solving

Ausbildung

Engineering degree

Tools

CAD software

Microsoft Office

Jobbeschreibung

Xstrahl, Brownhills, UK, is seeking a Graduate Production Quality Engineer to join the on-site production team. You will develop and maintain build manuals and work instructions, perform sign-off checks, and manage NCRs, CRs and related quality records to ensure traceability and compliance.

Working alongside experienced engineers on the shop floor, you will gain hands-on experience documenting processes, testing instructions, and supporting a regulated medical device environment, with