QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid in Crawley
QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid

QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid in Crawley

Crawley Full-Time 36000 - 60000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure quality compliance and lead internal audits for medical devices.
  • Company: Leading medical technology company in the UK with a focus on innovation.
  • Benefits: Hybrid work, competitive salary, vacation days, and private medical insurance.
  • Why this job: Join a mission-driven team improving healthcare through quality assurance.
  • Qualifications: Bachelor's degree in Engineering or Quality and experience in regulated environments.
  • Other info: Opportunity to make a real impact in the medical technology field.

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

A leading medical technology company in the UK is seeking a QA Engineer to support their Quality Management System. The role emphasizes regulatory compliance, particularly with ISO 13485, and involves leading internal audits, ensuring adherence to standards, and driving quality improvements.

Candidates should possess a Bachelor's degree in Engineering or Quality and relevant experience in a regulated environment. This position offers a hybrid work option along with competitive benefits including vacation days and private medical insurance.

QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid in Crawley employer: Elekta

As a leading medical technology company in the UK, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee growth and development. Our hybrid work model offers flexibility, while our commitment to quality and regulatory excellence ensures that you will be part of a team dedicated to making a meaningful impact in the healthcare sector. With competitive benefits such as vacation days and private medical insurance, we provide an environment where your contributions are valued and rewarded.
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Contact Detail:

Elekta Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid in Crawley

✨Tip Number 1

Network like a pro! Reach out to professionals in the medical technology field on LinkedIn. Join relevant groups and engage in discussions to get your name out there and learn about potential job openings.

✨Tip Number 2

Prepare for interviews by brushing up on ISO 13485 standards and quality management systems. We recommend creating a list of common interview questions and practising your responses to showcase your expertise.

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds!

✨Tip Number 4

Apply through our website for the best chance at landing that QA Engineer role! We make it easy for you to showcase your skills and experience directly to hiring managers.

We think you need these skills to ace QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid in Crawley

ISO 13485
Quality Management System
Regulatory Compliance
Internal Audits
Quality Improvements
Bachelor's degree in Engineering or Quality
Experience in a Regulated Environment
Attention to Detail

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience with ISO 13485 and any relevant audits you've led. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in medical devices and how you can contribute to our team. Keep it concise but impactful.

Showcase Your Regulatory Knowledge: Since this role focuses on regulatory compliance, make sure to mention any specific experiences or projects where you ensured adherence to standards. We love candidates who understand the importance of quality in healthcare!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates!

How to prepare for a job interview at Elekta

✨Know Your ISO 13485 Inside Out

Make sure you brush up on ISO 13485 standards before the interview. Be ready to discuss how you've applied these regulations in your previous roles, especially in audits and compliance. This shows you're not just familiar with the standards but can also implement them effectively.

✨Showcase Your Audit Experience

Prepare specific examples of internal audits you've led or participated in. Highlight any challenges you faced and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills, which are crucial for the role.

✨Emphasise Quality Improvements

Think about instances where you've driven quality improvements in your past positions. Be ready to share measurable outcomes from your initiatives. This will illustrate your proactive approach to quality management and your commitment to continuous improvement.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's quality management system and their approach to regulatory compliance. This not only shows your interest in the role but also helps you gauge if the company aligns with your values and career goals.

QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid in Crawley
Elekta
Location: Crawley
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  • QA Engineer - Medical Devices (ISO 13485 Audits) Hybrid in Crawley

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

    Elekta

    1000-5000
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