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- Tasks: Own ISO 13485 QMS activities and support regulatory compliance in medical devices.
- Company: Dynamic medical device company with a focus on quality and innovation.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Why this job: Deepen your quality experience while gaining valuable regulatory exposure.
- Qualifications: 3 years in a Quality role with knowledge of ISO 13485 and GMP.
- Other info: Join a supportive team and make a real impact in healthcare.
The predicted salary is between 36000 - 60000 £ per year.
A great opportunity for a QARA professional to step into a hands-on role within a medical device environment. Hybrid (up to 2 days WFH) near Bristol. This role sits at the heart of manufacturing, supplier oversight and regulatory support, with a strong quality focus (70%) and exposure to UK, EU and global regulatory activities (30%).
What you’ll be doing:
- Day-to-day ownership of ISO 13485 / GMP-aligned QMS activities
- Supporting validation (equipment, process & software)
- Managing and supporting internal, supplier & Notified Body audits
- Handling complaints, RCA and CAPAs
- Maintaining controlled documentation within an eQMS
- Supporting supplier quality and production quality activities
- Contributing to regulatory documentation, PMS and labelling reviews
What we’re looking for:
- 3 years’ experience in a Quality role within medical devices
- Working knowledge of ISO 13485, GMP and medical device regulations (MDR / UK MDR / FDA exposure a plus)
- Experience across validation, audits, complaints and document control
- Someone confident working independently, detail-driven and solutions-focused
This is a strong role for someone looking to deepen their medical device quality experience while gaining broader regulatory exposure.
Travel Specialist (Homeworking) employer: GxPeople Global
Contact Detail:
GxPeople Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Travel Specialist (Homeworking)
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on ISO 13485 and GMP standards. We recommend creating a cheat sheet of key points and examples from your experience to showcase your expertise during the chat.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest using our website to find roles that excite you and match your skills perfectly.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm and professionalism, which is always a plus in the hiring process.
We think you need these skills to ace Travel Specialist (Homeworking)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Travel Specialist role. Highlight your experience in quality roles, especially within medical devices, and showcase your knowledge of ISO 13485 and GMP. We want to see how your skills align with 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 this role and how your background makes you a perfect fit. Don’t forget to mention any specific experiences that relate to regulatory support and audits.
Showcase Your Attention to Detail: Since this role is detail-driven, make sure your application is free from typos and errors. We appreciate candidates who take the time to present their information clearly and accurately. It reflects your commitment to quality!
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come directly from our site!
How to prepare for a job interview at GxPeople Global
✨Know Your Standards
Make sure you brush up on ISO 13485 and GMP regulations before the interview. Being able to discuss these standards confidently will show that you’re not just familiar with them, but that you understand their importance in a medical device environment.
✨Showcase Your Experience
Prepare specific examples from your past roles that highlight your experience with audits, complaints, and document control. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.
✨Be Solutions-Focused
Since the role requires a detail-driven and solutions-focused mindset, think of challenges you've faced in previous positions and how you overcame them. This will demonstrate your problem-solving skills and ability to work independently.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s quality management systems and regulatory processes. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
