At a Glance
- Tasks: Manage supplier quality and ensure compliance with regulatory standards in a dynamic environment.
- Company: Join a fast-growing medical device company making a real difference in patient lives.
- Benefits: Enjoy hybrid working, competitive salary, private healthcare, and generous annual leave.
- Other info: Opportunity for international travel and excellent career growth.
- Why this job: Be part of a purpose-driven team developing life-changing technology.
- Qualifications: Degree in engineering and experience in supplier quality within regulated industries.
The predicted salary is between 40000 - 50000 £ per year.
I'm currently working with an innovative and fast-growing medical device organisation in Oxfordshire that's looking to appoint a Supplier Quality Engineer as part of its continued expansion. This is a fantastic opportunity to join a purpose-driven business developing sophisticated implantable technology that genuinely improves patient lives. The company operates in a highly regulated environment and is moving into an exciting stage of clinical and manufacturing growth.
The Opportunity
As Supplier Quality Engineer, you will take ownership of the supplier quality management programme, working closely with Engineering, Manufacturing and Quality teams to ensure suppliers consistently meet regulatory, technical and quality requirements. The role offers a hybrid working model, typically 3 days per week on site at a state-of-the-art Oxfordshire facility, with regular UK and international travel to supplier sites.
Key Responsibilities
- Lead supplier evaluation and onboarding activities
- Plan and conduct supplier audits (remote and on-site)
- Manage supplier quality agreements and corrective actions (SCARs)
- Act as the quality interface between suppliers and internal R&D and Manufacturing Engineering teams
- Support design for manufacture through quality input into design reviews and risk management
- Oversee supplier CAPAs, non-conformances and complaint investigations
- Support internal audits and preparation for external inspections
- Analyse and report supplier performance trends to senior stakeholders
- Ensure supplier compliance with ISO 13485 and FDA 21 CFR Part 820
- Support supplier process validations (IQ/OQ/PQ) and capability studies (Cp/Cpk)
- Where required, spend short periods working directly at supplier sites to oversee quality-critical work
What I'm Looking For
Essential:
- Degree in an engineering discipline (Mechanical, Biomedical, Electrical, Industrial or similar)
- Proven experience in supplier quality engineering within a regulated industry (medical devices, aerospace, defence, etc.)
- Strong experience conducting external supplier audits
- Solid understanding of CAPA, non-conformances, complaints and change control
- Ability to interpret engineering drawings, tolerances and specifications
- Willingness to travel regularly in the UK and internationally
Desirable:
- ISO Lead Auditor certification
- Six Sigma Green Belt (or above)
- Experience with medical device materials and manufacturing processes
- Knowledge of ISO 13485, MDR, UKCA and FDA 21 CFR Part 820
You’ll suit this role if you’re confident dealing with suppliers, enjoy working cross-functionally, and thrive in a fast-paced, collaborative environment.
What's On Offer
- Competitive salary based on experience
- Hybrid working model
- Private healthcare
- Life assurance and income protection
- Company pension scheme
- Equity participation scheme
- 27 days annual leave plus bank holidays
- The chance to play a key role in delivering genuinely life-changing technology
If you're a Supplier Quality Engineer looking for your next step in a growing medical device business, I'd love to talk you through the role in more detail.
Supplier Quality Engineer employer: ProTech Recruitment Ltd
Contact Detail:
ProTech Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Supplier Quality Engineer
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical device industry and let them know you're on the hunt for a Supplier Quality Engineer role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO 13485 and FDA regulations. Be ready to discuss how your experience aligns with the responsibilities of the role, especially around supplier audits and CAPA management. Show them you mean business!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that resonate with your values. Check out our website for opportunities that match your skills and passion for improving patient lives. Tailor your approach to each company’s mission and culture.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from your conversation to show your genuine interest in the role and the company.
We think you need these skills to ace Supplier Quality Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Supplier Quality Engineer role. Highlight your experience in supplier quality engineering and any relevant qualifications, like your degree or certifications. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about working in the medical device industry and how you can contribute to our purpose-driven mission. Keep it concise but impactful – we love a good story!
Showcase Relevant Experience: When filling out your application, be sure to showcase your experience with supplier audits, CAPA processes, and any regulatory knowledge you have. We’re keen on seeing how you've tackled challenges in previous roles, especially in regulated environments.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about our company culture and values.
How to prepare for a job interview at ProTech Recruitment Ltd
✨Know Your Stuff
Make sure you brush up on your knowledge of ISO 13485 and FDA regulations. Familiarise yourself with the specific requirements for supplier quality management in the medical device industry, as this will show that you're serious about the role and understand the regulatory landscape.
✨Showcase Your Experience
Prepare to discuss your previous experience with supplier audits and CAPA processes. Have specific examples ready that demonstrate how you've successfully managed supplier quality issues in the past, as this will highlight your hands-on expertise.
✨Ask Smart Questions
Think of insightful questions to ask during the interview. Inquire about the company's approach to supplier evaluation and onboarding, or how they handle non-conformances. This shows your interest in the role and helps you gauge if the company is the right fit for you.
✨Be Ready to Travel
Since the role involves regular travel to supplier sites, be prepared to discuss your flexibility and willingness to travel. Highlight any previous experiences where you've had to adapt to different environments, as this will reassure them of your commitment to the role.