Are you a Quality Technician ready for your next challenge? Or perhaps you've recently completed an Engineering, Manufacturing or Quality-related degree/HNC and have gained some hands-on industry experience?

If you're looking for a role where you'll do more than just tick boxes and file paperwork, this could be the perfect opportunity.

We're looking for a Quality & Test Engineer to join our clients growing team, working at the forefront of medical device manufacturing. You'll gain exposure to everything from ISO 13485 quality systems and product testing through to audits, investigations, CAPA activities and continuous improvement projects – all while being mentored by an experienced Senior Quality Manager.

This is an opportunity to build a genuine career in quality engineering within a highly regulated industry where quality truly matters.

No two days are the same in this hands-on role. You'll be involved in:

• Supporting quality activities across manufacturing and operations
• Conducting inspections, verification activities and pressure vessel testing
• Investigating non-conformances and supporting root cause analysis
• Assisting with CAPA activities and continuous improvement projects
• Maintaining quality records, documentation and audit-ready systems
• Supporting internal, customer and regulatory audits
• Working closely with Engineering, Production and Supply Chain teams
• Analysing quality data, identifying trends and helping drive improvements

You'll gain practical experience across the full quality lifecycle while developing valuable skills within a regulated medical device environment.

We're open to candidates from a variety of backgrounds, including:

• Quality Technicians looking to progress into an engineering-focused role
• Individuals with 1–2 years' experience in manufacturing, quality, testing or engineering support environments with a Degree, HNC or HND in Engineering, Manufacturing
• Candidates who have completed relevant placements, internships or apprenticeships

You'll stand out if you have:

• A keen eye for detail and a passion for quality
• Strong organisational and communication skills
• Experience working within a manufacturing or regulated environment
• Exposure to quality systems, inspections, testing or compliance activities
• A proactive attitude and eagerness to learn

Experience with ISO 13485, CAPA, audits, pressure testing or medical devices would be advantageous but is not essential.

This is more than just a job – it's a development opportunity.

You'll receive ongoing support and mentoring from an experienced Senior Quality Manager while gaining exposure to:

• Medical device quality systems
• ISO 13485 compliance
• Product and pressure vessel testing
• CAPA and non-conformance investigations
• Internal and external audits
• Continuous improvement methodologies
• Cross-functional engineering collaboration

Most importantly, you'll have a clear pathway to develop your career as your skills and experience grow.

If you're looking for a role where you can learn, develop and make a real impact in a quality-focused organisation, we'd love to hear from you.