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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 working hours, training opportunities, and competitive salary.
- Why this job: Make a significant impact in a small team with strategic responsibilities.
- Qualifications: Quality background required; ISO 13485 audit experience preferred.
- Other info: International travel is minimal, only once a 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
- Quality background - Does not need to have been a manager previously
- ISO 13485 Audit experience
Quality Manager - ISO 13485 employer: Revorec Recruitment Solutions
Contact Detail:
Revorec Recruitment 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 in the medical devices sector.
✨Tip Number 2
Network with professionals in the medical devices industry, especially those who have experience in quality management. Attend relevant conferences or webinars to make connections and gain insights that could give you an edge in your application.
✨Tip Number 3
Prepare to discuss your experience with audits, both internal and external. Be ready to share specific examples of how you've contributed to quality assurance processes, as this will be a key focus for the hiring team.
✨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 during interviews, showing that you're genuinely interested in contributing to their success.
We think you need these skills to ace Quality Manager - ISO 13485
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality management, particularly with ISO 13485. Include specific examples of audits you've conducted and any leadership roles you've held, even if they weren't formal management positions.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention how your background aligns with their needs, especially your experience with quality assurance and control in a clean room environment.
Highlight Relevant Skills: Emphasise skills that are crucial for the Quality Manager position, such as attention to detail, strategic thinking, and your ability to manage a small team. Use specific examples to demonstrate these skills in action.
Proofread Your Application: Before submitting, carefully proofread your application materials. Look for any spelling or grammatical errors, and ensure that all information is clear and concise. A polished application reflects your professionalism.
How to prepare for a job interview at Revorec Recruitment Solutions
✨Understand ISO 13485 Inside Out
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 Your 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 where you successfully navigated audit challenges or improved processes.
✨Express Your Vision for Quality Management
This role offers autonomy, so be ready to share your ideas on how you would enhance the quality management system. Discuss any innovative strategies you might implement to improve QA and QC processes.
