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- Tasks: Lead the Quality Management System and ensure compliance with global regulations.
- Company: Exciting Medtech start-up focused on innovation and patient safety.
- Benefits: Remote work, competitive salary, and a chance to shape quality strategy.
- Why this job: Make a real impact in the medical device industry and ensure product compliance.
- Qualifications: 8+ years in Quality/Compliance with a degree in relevant fields.
- Other info: Opportunity for career growth and travel for audits and inspections.
The predicted salary is between 48000 - 72000 £ per year.
This range is provided by GxPeople Global. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
Direct message the job poster from GxPeople Global
Building Life Science teamsferoze.malik@gxpeople.com020 8135 6831
An innovative MedTech startup in London looking for a Senior Quality Engineer to help build and lead their Quality Management System (ISO 13485) and support the development of their first implantable medical device.
You’ll work closely with the design teams to ensure products are developed in a controlled, compliant, and scalable way contributing directly to the company’s mission to transform neurological care through cutting-edge silicon-based technology.
What you’ll be doing:
- Own and maintain QMS processes in line with ISO 13485
- Lead QMS remediation and eQMS implementation projects
- Oversee supplier qualification, goods handling, and documentation compliance
- Champion quality culture across engineering and operations
What you’ll need:
- 4+ years’ experience in Quality Engineering within medical devices
- Deep knowledge of ISO 13485 and design controls
- Essential: experience working with integrated circuits or silicon-based technologies
- Strong documentation, organisational, and process-driven mindset
- Hands-on approach and comfort in a complex engineering environment
If you’re a MedTech QA professional who thrives in a hands-on, fast-paced setting — and want to help bring life-changing technology to market please apply to the advert or get in touch for more details.
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Full-time
Job function
-
Job function
Quality Assurance
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Industries
Medical Equipment Manufacturing
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Senior Quality Engineer employer: GxPeople Global
Contact Detail:
GxPeople Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior 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 Senior 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 other relevant regulations. We recommend creating a cheat sheet of key points and examples from your experience that showcase your expertise in quality management systems.
✨Tip Number 3
Don’t just wait for job postings to come to you! Actively search for companies that align with your values and goals, and reach out directly. A well-crafted email expressing your interest can sometimes lead to opportunities that aren’t even advertised yet.
✨Tip Number 4
Finally, apply through our website! We’ve got a streamlined process that makes it easy for you to submit your application. Plus, it shows you’re serious about joining our team and helps us keep track of your application more efficiently.
We think you need these skills to ace Senior Quality Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Quality Engineer role. Highlight your experience with ISO 13485 and any relevant projects you've led. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality systems in the medical device sector. Share specific examples of your achievements that relate to the job description.
Showcase Your Leadership Skills: Since this role involves leading audits and managing compliance, make sure to highlight your leadership experience. We love to see how you've driven initiatives and improved processes in your previous roles.
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’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at GxPeople Global
✨Know Your QMS Inside Out
Make sure you’re well-versed in ISO 13485 and the specifics of Quality Management Systems. Brush up on your knowledge of design controls, risk management, and CAPA processes. Being able to discuss these topics confidently will show that you’re ready to take ownership of the QMS.
✨Showcase Your Leadership Skills
Prepare examples from your past experiences where you led audits or managed compliance initiatives. Highlight how you’ve driven continuous improvement and handled regulatory inspections. This will demonstrate your capability to lead and influence within a quality framework.
✨Understand the Regulatory Landscape
Familiarise yourself with the latest regulations and standards relevant to medical devices and combination products. Be ready to discuss how you’ve navigated these in previous roles, especially regarding GMP and GDP compliance. This knowledge will set you apart as a candidate who is proactive and informed.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s quality strategy and how they approach supplier oversight and risk assessments. This not only shows your interest in the role but also gives you insight into their operations and culture, helping you determine if it’s the right fit for you.
