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- Tasks: Ensure medical devices meet quality standards and regulations through detailed inspections.
- Company: Fast-growing medical device manufacturer in Oxford with a focus on innovation.
- Benefits: Full-time role with hands-on experience in a critical industry.
- Why this job: Be the last line of defence for patient safety and product integrity.
- Qualifications: 2+ years in quality inspection, knowledge of ISO 13485 and GMP required.
- Other info: Join a dynamic team with opportunities for professional growth.
The predicted salary is between 36000 - 60000 £ per year.
Job Title: Medical Device Quality Inspector
Location: On-Site, Oxford, United Kingdom
Employment Type: FTC – 6 months, Full Time
Role:
A fast-growing and innovation-driven medical device manufacturer based in Oxford is hiring for a Quality Inspector.
This company has seen consistent growth in regulated markets and is now seeking a Quality Inspector with a strong grounding in ISO 13485 and GMP principles to support its production quality assurance operations. This is a key hire in the Quality function. This role is ideal for someone who thrives in a hands-on, precision-focused environment and takes pride in being the last line of defence before a device reaches the patient, as well as being highly detail-oriented.
The Opportunity:
This role will place you right at the heart of the quality operations, working alongside engineering, manufacturing, and quality teams to ensure every device released is fully compliant with internal procedures and global regulatory expectations. You’ll be conducting in-process and final inspections on Class II devices, contributing directly to patient safety and product integrity.
Key Responsibilities:
- Perform in-process, final release, and incoming goods inspections in accordance with ISO 13485 and company SOPs
- Review DHRs and batch documentation for completeness and compliance
- Use of precision measuring equipment to verify critical dimensions and tolerances
- Document and escalate any NCRs, support root cause investigations and CAPA
- Liaise with production and QA teams to support continuous improvement in inspection protocols and process efficiency
- Maintain accurate inspection records in accordance with GMP and data integrity expectations
- Contribute to internal audits and support regulatory inspections when required
Requirements:
- Minimum 2+ years’ experience in a Quality Inspector or QA Technician role within the medical device or life sciences sector
- Strong working knowledge of ISO 13485, 21 CFR Part 820, and GMP
- Competent in the use of mechanical inspection tools and visual inspection techniques
- Familiarity with documentation review and batch release processes
- Attention to detail with a methodical, risk-based approach to quality
Quality Inspector employer: Skills Alliance
Contact Detail:
Skills Alliance Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Inspector
✨Tip Number 1
Network like a pro! Reach out to folks in the medical device industry on LinkedIn or at local meetups. We all know that sometimes it’s not just what you know, but who you know that can help you land that Quality Inspector role.
✨Tip Number 2
Prepare for interviews by brushing up on ISO 13485 and GMP principles. We suggest creating a cheat sheet of key points and examples from your past experience. This way, you’ll be ready to impress with your knowledge and hands-on skills!
✨Tip Number 3
Don’t forget to showcase your attention to detail! During interviews, share specific instances where your meticulous nature made a difference in quality assurance. We want to hear about those moments when you were the last line of defence!
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take the initiative to connect directly with us. Let’s get you that Quality Inspector position!
We think you need these skills to ace Quality Inspector
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Inspector role. Highlight your experience with ISO 13485 and GMP principles, as well as any hands-on inspection work you've done. 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 quality assurance in the medical device sector. Share specific examples of how you've contributed to patient safety and product integrity in previous roles.
Show Off Your Attention to Detail: As a Quality Inspector, attention to detail is key. In your application, make sure to showcase instances where your meticulous nature has made a difference. Whether it's through documentation review or using precision measuring equipment, let us know how you ensure quality.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at Skills Alliance
✨Know Your Standards
Make sure you brush up on ISO 13485 and GMP principles before the interview. Being able to discuss these standards confidently will show that you understand the core requirements of the role and can hit the ground running.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've conducted inspections or dealt with non-conformance reports. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your attention to detail.
✨Familiarise Yourself with the Company
Research the company’s products and their impact on patient safety. Understanding their mission and values will help you align your answers with what they’re looking for in a Quality Inspector.
✨Ask Insightful Questions
Prepare thoughtful questions about their quality assurance processes and how they handle continuous improvement. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
