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For Companies At a Glance
- Tasks: Support QMS maintenance, write SOPs, and assist with QA/RA functions.
- Company: Join a leading Medical Device Manufacturer committed to quality standards.
- Benefits: Enjoy a competitive salary, supportive leadership, and career growth opportunities.
- Why this job: Be part of a nurturing team that values your development in a vital industry.
- Qualifications: Basic understanding of QMS in Medical Devices; related scientific or technical education required.
- Other info: This role is perfect for those looking to make an impact in healthcare.
The predicted salary is between 30000 - 42000 £ per year.
Join a truly supportive team with a chance to develop and grow within the business.
About Our Client
Our client is a Medical Device Manufacturer, working to MDR and ISO 13485 Standards.
Job Description
- Support the maintenance of QMS by writing and assisting with SOPs and related documentation
- Support the broader QA/RA functions as required
- Review batch records and assist with release activities
The Successful Applicant
- Basic understanding of QMS in Medical Devices or a regulated industry
- Educated in a related Scientific/Technical discipline
What’s on Offer
- Competitive salary and benefits
- Supportive leadership
- Significant potential for career growth and development
QMS Technician - Medical Devices employer: Page Personnel
Contact Detail:
Page Personnel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QMS Technician - Medical Devices
✨Tip Number 1
Familiarise yourself with ISO 13485 standards and the Medical Device Regulation (MDR). Understanding these regulations will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the medical device industry, especially those involved in Quality Management Systems. Engaging with them on platforms like LinkedIn can provide insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to quality assurance or regulatory compliance in previous roles. This will showcase your practical experience and understanding of QMS.
✨Tip Number 4
Research the company’s products and recent developments in the medical device sector. Being knowledgeable about their offerings will help you stand out during the interview process.
We think you need these skills to ace QMS Technician - Medical Devices
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a QMS Technician in the medical devices sector. Familiarise yourself with terms like QMS, SOPs, and ISO 13485 standards.
Tailor Your CV: Highlight your relevant experience and education in your CV. Emphasise any previous work in quality management systems or regulated industries, and ensure your qualifications align with the job requirements.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for quality assurance in medical devices. Mention specific experiences that demonstrate your understanding of QMS and how you can contribute to the team.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the QMS field.
How to prepare for a job interview at Page Personnel
✨Understand QMS Fundamentals
Make sure you have a solid grasp of Quality Management Systems, especially in the context of medical devices. Brush up on ISO 13485 standards and be ready to discuss how they apply to your previous experiences.
✨Prepare for Technical Questions
Expect questions that assess your technical knowledge related to QMS and regulatory compliance. Review common scenarios or challenges faced in the industry and think about how you would address them.
✨Showcase Your Documentation Skills
Since the role involves writing SOPs and related documentation, be prepared to discuss your experience with technical writing. Bring examples of documents you've created or contributed to in the past.
✨Demonstrate Team Collaboration
Highlight your ability to work within a team, especially in QA/RA functions. Share examples of how you've collaborated with others to achieve quality objectives or resolve issues in a regulated environment.
