Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid)
Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid)

Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid)

Full-Time 36000 - 60000 Β£ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead the development of a Quality Management System for medical devices and manage internal audits.
  • Company: A leading medical devices firm in the UK with a focus on quality and compliance.
  • Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
  • Why this job: Make a difference in healthcare by ensuring the highest quality standards in medical devices.
  • Qualifications: Experience in the Medical Devices Industry and strong knowledge of ISO 13485.
  • Other info: Join a dynamic team dedicated to innovation and quality in healthcare.

The predicted salary is between 36000 - 60000 Β£ per year.

A medical devices firm in the UK is seeking a Quality Manager to develop their Quality Management System in accordance with ISO 13485. This role involves both remote and office-based responsibilities, with key tasks including managing internal audits and ensuring compliance with regulatory standards.

Candidates should have proven experience in the Medical Devices Industry and a strong understanding of quality management processes.

Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid) employer: Guided Solutions

Join a leading medical devices firm in the UK that prioritises employee development and fosters a collaborative work culture. With a hybrid working model, you will enjoy the flexibility of remote work while being part of a dynamic team dedicated to innovation and quality. The company offers comprehensive benefits, ongoing training opportunities, and a commitment to compliance and excellence, making it an ideal place for professionals seeking meaningful and rewarding careers in the medical sector.
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Contact Detail:

Guided Solutions Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid)

✨Tip Number 1

Network like a pro! Reach out to your connections in the medical devices industry and let them know you're on the hunt for a Quality Manager role. You never know who might have the inside scoop on job openings or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by brushing up on ISO 13485 and quality management processes. We recommend creating a list of common interview questions related to quality management and practising your answers. This will help you feel more confident when discussing your experience.

✨Tip Number 3

Showcase your expertise! During interviews, be ready to share specific examples of how you've successfully managed internal audits and ensured compliance with regulatory standards in your previous roles. This will demonstrate your hands-on experience and make you stand out.

✨Tip Number 4

Don't forget to apply through our website! We make it super easy for you to find and apply for Quality Manager positions. Plus, it shows you're serious about joining our team and helps us keep track of your application.

We think you need these skills to ace Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid)

Quality Management System (QMS)
ISO 13485
Internal Audits
Regulatory Compliance
Medical Devices Industry Experience
Quality Management Processes
Attention to Detail
Analytical Skills

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in the Medical Devices Industry and your understanding of ISO 13485. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality management and how you can contribute to our team. We love seeing candidates who can connect their personal values with our mission.

Showcase Your Audit Experience: Since managing internal audits is a key part of the role, make sure to highlight any relevant audit experience you have. We’re looking for candidates who can demonstrate their ability to ensure compliance with regulatory standards.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team!

How to prepare for a job interview at Guided Solutions

✨Know Your ISO 13485 Inside Out

Make sure you have a solid grasp of ISO 13485 and its implications for quality management in medical devices. Be prepared to discuss how you've applied these standards in your previous roles, as this will show your expertise and relevance to the position.

✨Showcase Your Audit Experience

Since managing internal audits is a key part of the role, come ready with examples of audits you've conducted. Highlight any challenges you faced and how you overcame them, as this demonstrates your problem-solving skills and attention to detail.

✨Understand Regulatory Compliance

Familiarise yourself with the regulatory landscape surrounding medical devices in the UK. Be prepared to discuss how you ensure compliance in your work, as this will reassure the interviewers that you can maintain high standards in their Quality Management System.

✨Prepare Questions About the Company

Research the company and prepare thoughtful questions about their current quality management practices and future goals. This shows your genuine interest in the role and helps you assess if the company aligns with your career aspirations.

Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid)
Guided Solutions
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  • Quality Manager, Medical Devices: ISO 13485 QMS (Hybrid)

    Full-Time
    36000 - 60000 Β£ / year (est.)
  • G

    Guided Solutions

    50-100
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