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- Tasks: Lead quality management and audits in a dynamic medical devices environment.
- Company: Join a pioneering medical devices manufacturer known for innovation and excellence.
- Benefits: Enjoy flexible hours, training opportunities, and competitive salary with great perks.
- Why this job: Make a real impact in a small team while shaping quality standards in the industry.
- Qualifications: Quality background required; ISO 13485 audit experience preferred but not mandatory.
- Other info: Opportunity for strategic input and minimal international travel.
The predicted salary is between 48000 - 84000 £ per year.
Didcot
£60,000 - £70,000 + Training + Flexi Time + Benefits
Are you a Quality Engineer, QA or similar looking to step up or a Quality Manager seeking a change? Do you want a strategic level position offering variety, a small team to manage and autonomy to put your own stamp on things?
The company are a respected Medical Devices manufacturer working at the cutting edge of industry advancements. Due to their pioneering capabilities they work with a range of products and with some impressive organisations both in the UK and internationally.
The role involves being accountable for Quality Management including QA and QC work in a clean room facility with a small team reporting to you. You will conduct both internal and external audits, but international travel is only once per year. It is a Monday to Friday role but start and finish times are flexible.
Here is a great chance to join a specialist where you will be a big fish in a small pond, have strategic input and a role you can really make your own.
The Role:
- Quality Manager
- ISO 13485 Audits - Internal and External for supply chain
- 37 hours Monday to Friday
Candidate Requirements:
- Quality background - Does not need to have been a manager previously
- ISO 13485 Audit experience
Quality Manager - ISO 13485 employer: Elix Sourcing Solutions
Contact Detail:
Elix Sourcing Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Manager - ISO 13485
✨Tip Number 1
Familiarise yourself with ISO 13485 standards and recent updates. Being well-versed in these regulations will not only boost your confidence during interviews but also demonstrate your commitment to quality management.
✨Tip Number 2
Network with professionals in the medical devices industry. Attend relevant conferences or webinars where you can meet potential colleagues or mentors who can provide insights into the company culture and expectations.
✨Tip Number 3
Prepare to discuss your experience with audits, both internal and external. Be ready to share specific examples of how you've successfully managed quality processes or resolved issues in previous roles.
✨Tip Number 4
Research the company’s products and their impact on the industry. Understanding their innovations and challenges will allow you to tailor your conversation and show how you can contribute to their success.
We think you need these skills to ace Quality Manager - ISO 13485
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Quality Manager position. Highlight key skills such as ISO 13485 audit experience and quality management.
Tailor Your CV: Customise your CV to reflect your relevant experience in quality management and any specific ISO standards you have worked with. Use keywords from the job description to make your application stand out.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality management and your ability to lead a team. Mention specific achievements related to ISO 13485 audits and how you can contribute to the company's success.
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 for a Quality Manager role.
How to prepare for a job interview at Elix Sourcing Solutions
✨Understand ISO 13485 Thoroughly
Make sure you have a solid grasp of ISO 13485 standards and how they apply to quality management in medical devices. Be prepared to discuss your experience with audits and how you've implemented these standards in previous roles.
✨Showcase Leadership Skills
Even if you haven't been a manager before, highlight any experiences where you've led projects or teams. Discuss how you can motivate and guide a small team, as this role involves managing others.
✨Prepare for Audit Scenarios
Expect questions about how you would handle internal and external audits. Think of specific examples from your past experiences that demonstrate your ability to conduct thorough audits and address any issues that arise.
✨Express Your Vision
This role offers autonomy, so be ready to share your ideas on how you would improve quality management processes. Discuss how you plan to put your own stamp on the role and contribute to the company's success.
