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- Tasks: Manage supplier quality, drive projects, and ensure top-notch performance metrics.
- Company: Smith+Nephew designs tech that enhances lives—join us in making a difference!
- Benefits: Enjoy flexible holidays, private health plans, and discounts on gyms and more.
- Why this job: Make a real impact on products while working in a diverse and inclusive culture.
- Qualifications: Experience in quality or engineering roles; knowledge of medical device regulations is a plus.
- Other info: Hybrid working model with hands-on training and mentorship opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living.
Join us as a Supplier Quality Engineer , where you’ll be handling supplier quality and performance, driving project-based initiatives, and ensuring our metrics and key performance indicators are always on point.
We’re seeking someone with strong analytical, project management, and communication skills. The ideal candidate will excel at monitoring project timelines and maintaining high quality standards. You’ll find no two days are the same as you’ll be working on multiple streams of work, with your key focus being ensuring we never compromise on quality. This role has the ability to have a real impact on the products we make for our customers.
What will you be doing?
In this role, you’ll handle supplier set up and approval processes, work on supplier changes with third-party suppliers, and collate data for business reporting and trend analysis. You’ll make decisions regarding supplier risk assessments, regulatory compliance and technical agreements while ensuring relevant standards and regulations.
You will also get hands on with the below:
- Collate, interpret and report data from multiple sources to support business reporting.
- Support supplier change requests, project programmes and associated change controls.
- Perform supplier set up and approval requirements.
- Support supplier risk assessments and management.
- Manage Supplier Quality Agreements and Approved Supplier Lists.
- Contribute to continuous improvement activities, including improvements to local procedural requirements.
What will you need to be successful?
You’ll need proven experience in a quality or engineering related role. Experience with Medical Devices or Pharmaceuticals and an awareness of Medical Device Regulations, GMP, GDP, and ISO13485 are a huge bonus!
You. Unlimited
We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
- Inclusion, Diversity and Equity: Committed to Welcoming, Celebrating and Growing on Diversity, Learn more about our Employee Inclusion Groups on our website.
- Your Future: Generous annual bonus and pension Schemes, Save As You Earn share options.
- Work/Life Balance: Flexible Holidays 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.
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Supplier Quality Engineer employer: Smith & Nephew
Contact Detail:
Smith & Nephew Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Supplier Quality Engineer
✨Tip Number 1
Familiarize yourself with the specific quality standards and regulations relevant to the medical device industry, such as ISO13485 and GMP. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality standards.
✨Tip Number 2
Highlight any experience you have with supplier management and risk assessments. Be prepared to discuss specific examples of how you've successfully managed supplier relationships and ensured compliance with quality metrics in previous roles.
✨Tip Number 3
Showcase your analytical skills by preparing to discuss how you've used data to drive decisions in past projects. Being able to interpret and report data effectively is crucial for this role, so think of concrete examples where your analysis led to improvements.
✨Tip Number 4
Emphasize your project management abilities, especially in a fast-paced environment. Be ready to talk about how you've managed multiple projects simultaneously while ensuring that quality standards were never compromised.
We think you need these skills to ace Supplier Quality Engineer
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Supplier Quality Engineer position. Make sure you understand the key responsibilities and required skills, such as project management and analytical abilities.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in quality or engineering roles, particularly in the medical devices or pharmaceuticals sector. Mention any familiarity with regulations like GMP, GDP, and ISO13485.
Showcase Your Skills: Demonstrate your strong analytical and communication skills in your application. Provide specific examples of how you've successfully managed projects or improved quality standards in previous roles.
Tailor Your Application: Customize your CV and cover letter to reflect the values and mission of Smith+Nephew. Highlight your commitment to quality and continuous improvement, aligning your personal goals with the company's objectives.
How to prepare for a job interview at Smith & Nephew
✨Showcase Your Analytical Skills
Be prepared to discuss specific examples where you've used your analytical skills to solve problems or improve processes. Highlight any experience you have with data interpretation and reporting, as this is crucial for the role.
✨Demonstrate Project Management Experience
Since the role involves managing multiple projects, share your experiences in project management. Discuss how you've successfully monitored timelines and ensured quality standards in past projects.
✨Familiarize Yourself with Relevant Regulations
Brush up on Medical Device Regulations, GMP, GDP, and ISO13485. Being knowledgeable about these standards will show that you're serious about compliance and quality assurance.
✨Prepare for Behavioral Questions
Expect questions that assess your ability to work in a team and handle supplier relationships. Use the STAR method (Situation, Task, Action, Result) to structure your responses and provide clear examples of your past experiences.
