Quality Engineer

Goole, United Kingdom
Yesterday
Job Type
Permanent
Work Pattern
Full-time
Work Location
On-site
Seniority
Mid
Education
Degree
Posted
18 May 2026 (Yesterday)

Benefits

25 days holiday Pension Private healthcare

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.


Smith+Nephew is hiringQuality Engineers.

Join our team as a Quality Engineer and help bring our “Life Unlimited” purpose to life by ensuring the quality of life-changing medical devices.

You’ll take ownership of monitoring and improving quality performance through the effective application of statistical process control (SPC) and data-driven quality metrics, using insights to proactively identify risks, drive process stability, and enable continuous improvement.

Working closely with manufacturing, engineering, and NPI teams, you will help embed a culture of quality excellence and informed decision-making.

We’re looking for someone who combines strong technical capability with a proactive, problem-solving mindset. A strong understanding of quality principles is essential, with proven experience in process monitoring and delivering measurable process improvements.

What will you be doing?

  • Act as Quality Lead for a specific Manufacturing Value Stream.
  • Provide day‑to‑day quality engineering support to manufacturing, ensuring timely resolution of nonconformances.
  • Lead structured root cause analysis using Six Sigma and Lean problem‑solving tools (5 Why, Fishbone, DMAIC, 8D).
  • Assist manufacturing in establishing and maintaining process controls, inspection plans, and quality checkpoints.
  • Conduct Measurement System Analysis (MSA) including Gage R&R studies to ensure measurement reliability.
  • Use statistical analysis to identify trends and recommend preventive actions.
  • Independently support change control including risk assessments, verification/validation, and documentation review.
  • Evaluate the quality impact of product and process changes and ensure compliance with regulatory requirements.
  • Support readiness activities for introduction of new or updated products/processes into manufacturing.
  • Support maintenance of risk management files (PFMEA, DFMEA, hazard analysis) across the product lifecycle.
  • Develop and execute validation plans and protocols for manufacturing processes, equipment, and inspection methods.
  • Perform process capability analysis (Cp, Cpk) and contribute to statistical experiment design (DOE).
  • Act as subject matter expert during audits and support preparation activities.
  • Lead or contribute to CAPA initiatives with strong root cause analysis and verification of effectiveness.
  • Ensure excellent documentation aligned with GDP and regulatory expectations.
  • Collect, analyse, and interpret data related to quality performance (scrap, defects, yields, complaints).
  • Prepare and present quality metrics to cross‑functional stakeholders.
  • Lead and support Six Sigma–based continuous improvement projects focused on yield improvement, defect reduction, and process capability enhancement.
  • Conduct structured investigations into returned products and customer complaints.
  • Collaborate with suppliers, test labs, and engineering functions to resolve issues.
  • Partner with Manufacturing, R&D, NPI, DQA, process engineering and QC to apply quality principles across the product lifecycle.

What will you need to be successful?

  • Bachelor’s degree in Engineering, Science, or a related technical discipline required (eg, Chemical Engineering, Materials Science).
  • Experience in a regulated industry (medical devices preferred).
  • Demonstrated experience applying Six Sigma tools (e.g., DMAIC, MSA, SPC, DOE, capability analysis).
  • Experience conducting Measurement System Analysis and Gage R&R studies.
  • Experience with root cause analysis, validation, and risk management.
  • Strong analytical skills and ability to interpret technical data.
  • Effective communication and cross‑functional collaboration skills.

Preferred

Lean Six Sigma Green Belt certification

2–5 years of quality engineering experience in a regulated environment.

Experience with CAPA ownership and statistical data analysis.

Familiarity with design transfer and sustaining engineering processes.

You. Unlimited.
We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
Inclusion and Belonging: Committed to welcoming, celebrating and thriving on inclusion and belonging. Learn more about our Employee Inclusion Groups on our website (www.smith-nephew.com)
Your Future: Generous annual bonus and pension schemes, Save As You Earn share options.
Work/Life Balance: Flexible vacation and time off, paid holidays and paid volunteering hours, so we can give back to our communities.
Your Wellbeing: Private health and dental plans, healthcare cash plans, income protection, life assurance and much more.
Flexibility: Hybrid working model (for most professional roles).
Training: Hands-on, team-customised, mentorship.
Extra Perks: Discounts on gyms and fitness clubs, salary sacrifice bicycle and car schemes and many other employee discounts.

Hybrid role

Stay connected by joining our Talent Community.

We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day.


Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek intoYou. Unlimited., life, culture, and benefits at S+N.

Explore our website and learn more about our mission, our team, and the opportunities we offer.

Related Jobs

View all jobs
Spotlight

Lead Development Engineer

Corin Group Cirencester, gloucestershire, United Kingdom
On-site

Quality Engineer

Azenta Life Sciences Partington, Manchester, United Kingdom

Quality Engineer

White Label Recruitment Leeds, United Kingdom

Quality Engineer, Validation

OrganOx Oxford, United Kingdom
On-site

Quality Engineer - Manufacturing -Aerospace/Medical

Precept Recruit Southwell, Nottinghamshire, United Kingdom
On-site

Supplier Quality Engineer - Femtech - Oxford

Newton Colmore Oxford, Oxfordshire, United Kingdom
Hybrid

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Where to Advertise Medical Technology Jobs in the UK (2026 Guide)

Where to advertise medical technology jobs UK in 2026: the specialist boards and MDR/IEC 62304-aware channels that reach biomedical and medtech talent. The medtech candidate pool spans biomedical engineers, regulatory affairs specialists, clinical scientists, software engineers working within IEC 62304 and MDR frameworks, imaging scientists and commercial professionals with deep healthcare sector knowledge. General job boards consistently conflate medical technology with broader healthcare, pharmaceutical and IT roles — producing high application volumes but low candidate quality for specialist medtech positions. This guide, published by MedicalTechnologyJobs.co.uk, covers where to advertise medical technology roles in the UK in 2026, how the main platforms compare, what employers should expect to pay, and what the data says about hiring across different role types.

Medical Technology Jobs UK 2026: What to Expect Over the Next 3 Years

Medical Technology Jobs UK 2026: roles, salaries and the trends shaping UK medtech hiring over the next three years — devices, diagnostics and digital health. Medical technology is one of those rare sectors where commercial ambition and genuine human impact point in exactly the same direction. The devices, diagnostics, digital health platforms, and AI-powered clinical tools that medical technology companies develop do not just generate revenue — they extend lives, reduce suffering, and change what is possible inside the clinical encounter. That combination of purpose and commercial scale makes the medical technology jobs market one of the most compelling in the entire UK life sciences and technology landscape. And that market is changing faster than at any previous point in the sector's history. The integration of artificial intelligence into diagnostic imaging, pathology, and clinical decision support has moved from research demonstration to regulatory approval and NHS deployment. Wearable and implantable devices are generating continuous patient data at a scale that is transforming how chronic conditions are monitored and managed. Digital therapeutics — software that delivers clinically validated therapeutic interventions — have emerged as a recognised product category with its own regulatory pathway. Surgical robotics has moved from a premium offering at a handful of specialist centres to a mainstream surgical platform whose capabilities are expanding with each generation. For job seekers, the medical technology jobs market of 2026 represents an opportunity that is both broader and more technically demanding than it was three years ago. The roles being created now span a wider range of disciplines, require a more sophisticated understanding of the intersection between technology and clinical practice, and carry higher regulatory expectations than the medtech jobs of even a short time ago. This article breaks down what the UK medical technology jobs market is likely to look like through to 2028 — covering the titles emerging right now, the technologies driving employer demand, the skills that will matter most, and how to position your career ahead of the curve in one of the most consequential sectors in the UK economy.

How Many Medical Technology Tools Do You Need to Know to Get a Medical Technology Job?

Medical technology tools for UK medtech jobs in 2026: how many CAD, regulatory (ISO 13485, FDA), MATLAB and clinical software tools you really need on your CV. If you’re pursuing a career in medical technology, it can feel like the toolkit is endlessly long: imaging systems, data analysis software, regulatory platforms, testing frameworks, prototyping tools, CAD, quality management systems, signal processing libraries and more. Scroll job boards or LinkedIn, and it’s easy to think you need to know every tool under the sun just to secure an interview. Here’s the honest truth most hiring managers won’t explicitly tell you: 👉 They don’t hire you because you know every tool — they hire you because you understand the underlying principles and can apply the right tool in the right context to solve real problems. Tools matter — absolutely — but they are secondary to problem-solving ability, clinical awareness, engineering rigour and the ability to deliver safe, reliable solutions. So how many medical technology tools do you actually need to know to get a job? For most job seekers, the answer is far fewer than you think. This article explains what employers really want, which tools are core, which are role-specific, and how to focus your learning so you look confident, competent and end-game ready.