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- Tasks: Join a dynamic Quality team to maintain and enhance the QMS for a global IVD business.
- Company: A forward-thinking company where quality is genuinely valued and supported by leadership.
- Benefits: Enjoy a collaborative environment, stability in your role, and opportunities for hands-on improvements.
- Why this job: Be part of a respected team where your voice matters and quality is prioritised.
- Qualifications: Experience in regulated QMS environments and strong documentation skills are essential.
- Other info: Curious? Even if your CV isnât updated, letâs chat about this exciting opportunity!
The predicted salary is between 42000 - 70000 ÂŁ per year.
Quality Manager (Where Quality is Actually Valued) ÂŁ50,000+ | ISO 13485 | IVD
Letâs be honest, QA often gets a bad rap. You join a business where the CEO doesnât get it, teams see you as the âfun police,â and you spend more time firefighting than actually improving anything. This isnât that. This is a business where quality is genuinely backed by the CEO. The QMS? Itâs smooth. The audits? They fly through with minimal findings. The team? Longstanding, collaborative, and proud of the role they play.
About the Role
Youâll be joining a tight-knit Quality team of two, helping to maintain and evolve the QMS for a growing IVD business with global reach. The role involves both maintenance of the QMS and project based work so youâll have the stability of a structured system, with the variety of hands-on improvements too.
Maintenance Tasks Include:
- Document control
- Internal audits
- Reviewing audit findings
- Supplier approvals & oversight
- Equipment calibration
- Hosting customer audits
What Weâre Looking For:
This isnât about just enforcing rules. Itâs about bringing people along the journey, being agile and proactive. Weâre looking for someone who:
- Communicates clearly and confidently
- Understands the âwhyâ behind the standards
- Isnât wedded to a rigid, Big Pharma / MedTech QA mindset
Must-Have Skills:
- Experience in regulated QMS environments (ISO 13485 &/or 17025 ideally)
- Broad QA knowledge: NCs, deviations, CAPAs, change control, risk, investigations
- Internal & external audit experience
- Strong documentation and process improvement capabilities
Why This Role Stands Out:
- Quality is respected and resourced.
- No uphill battles here.
- Youâll be heard.
- The CEO wants to know whatâs going on in QA.
- Happy people stick around.
- The proof is in the team tenure.
Curious? Even if your CV isnât updated, letâs have a chat. This is the kind of role you feel when itâs right, and if youâve read this far, it might just be.
Quality System Manager employer: Medibeam
Contact Detail:
Medibeam Recruiting Team
StudySmarter Expert Advice đ¤Ť
We think this is how you could land Quality System Manager
â¨Tip Number 1
Network with professionals in the Quality Assurance field, especially those who have experience with ISO 13485. Attend industry events or webinars to connect with potential colleagues and learn more about the company culture.
â¨Tip Number 2
Research the company's current QMS practices and be prepared to discuss how your experience aligns with their needs. Understanding their specific challenges can help you demonstrate your value during conversations.
â¨Tip Number 3
Showcase your soft skills, particularly your ability to communicate clearly and confidently. Prepare examples of how you've successfully collaborated with teams to improve quality processes in previous roles.
â¨Tip Number 4
Be proactive in your approach. If you have ideas for improving their QMS or addressing common challenges in the industry, share them during your discussions. This will highlight your initiative and forward-thinking mindset.
We think you need these skills to ace Quality System Manager
Some tips for your application đŤĄ
Understand the Role: Read the job description thoroughly to grasp what the company is looking for in a Quality System Manager. Pay attention to the specific skills and experiences they value, such as knowledge of ISO 13485 and internal audit experience.
Tailor Your CV: Customise your CV to highlight relevant experience in regulated QMS environments. Emphasise your understanding of quality standards and any hands-on improvements you've implemented in previous roles.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for quality management. Use it to explain how your background aligns with the company's values and the importance of quality in their operations. Mention your ability to communicate clearly and work collaboratively.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application demonstrates attention to detail, which is crucial in quality management roles.
How to prepare for a job interview at Medibeam
â¨Understand the Company Culture
Before your interview, take some time to research the company's culture and values. Since this role emphasises a supportive environment where quality is valued, be prepared to discuss how you can contribute positively to that culture.
â¨Showcase Your Communication Skills
As the role requires clear and confident communication, think of examples from your past experiences where you effectively communicated complex quality concepts to non-QA teams. This will demonstrate your ability to bring people along on the journey.
â¨Demonstrate Your QMS Knowledge
Be ready to discuss your experience with ISO 13485 and other relevant standards. Prepare specific examples of how you've maintained or improved a Quality Management System in previous roles, highlighting your understanding of the 'why' behind the standards.
â¨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in QA, such as handling non-conformities or leading audits, and how you approached them. This will show your proactive mindset and adaptability.
