Software Quality Engineer – MedTech & Regulatory
Software Quality Engineer – MedTech & Regulatory

Software Quality Engineer – MedTech & Regulatory

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

  • Tasks: Ensure software quality in medical devices and guide compliance with industry standards.
  • Company: Leading biotechnology firm dedicated to enhancing patient health.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Make a real difference in healthcare by ensuring the quality of innovative technologies.
  • Qualifications: 3+ years in quality engineering and strong software development background.
  • Other info: Join a passionate team focused on improving patient outcomes.

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

A biotechnology company is looking for a Software Quality Engineer to provide crucial guidance on software quality processes. The role focuses on ensuring compliance with relevant standards in a medical device environment, including participation in risk management and regulatory submissions.

The ideal candidate will have a strong background in software development and at least 3 years of experience in quality engineering, with a solid understanding of industry regulations. This position offers an opportunity to contribute to innovative technologies that enhance patient health.

Software Quality Engineer – MedTech & Regulatory employer: Lenntech Search

Join a pioneering biotechnology company that prioritises innovation and excellence in the MedTech sector. With a strong commitment to employee development, we offer comprehensive training programmes and career advancement opportunities, all within a collaborative and inclusive work culture. Located in a vibrant area, our team enjoys a supportive environment where your contributions directly impact patient health and safety.
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Contact Detail:

Lenntech Search Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Software Quality Engineer – MedTech & Regulatory

Tip Number 1

Network like a pro! Reach out to professionals in the MedTech field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Software Quality Engineer role.

Tip Number 2

Prepare for those interviews! Brush up on your knowledge of software quality processes and industry regulations. We recommend practising common interview questions related to risk management and compliance to show you’re the perfect fit.

Tip Number 3

Showcase your experience! When you get the chance, highlight your background in software development and quality engineering. We want to see how your skills align with the innovative technologies we’re working on.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re excited to see how you can contribute to enhancing patient health with us!

We think you need these skills to ace Software Quality Engineer – MedTech & Regulatory

Software Quality Assurance
Regulatory Compliance
Risk Management
Quality Engineering
Medical Device Standards
Software Development
Industry Regulations
Technical Documentation

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in software quality engineering, especially in the MedTech field. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects and achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about software quality in the medical device industry. We love seeing candidates who can connect their personal motivations to our mission of enhancing patient health.

Showcase Your Regulatory Knowledge: Since this role involves compliance with industry regulations, make sure to mention any specific standards you’re familiar with. We appreciate candidates who can demonstrate their understanding of risk management and regulatory submissions.

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 from us!

How to prepare for a job interview at Lenntech Search

Know Your Standards

Familiarise yourself with the relevant software quality standards in the MedTech industry, such as ISO 13485 and IEC 62304. Being able to discuss these standards confidently will show that you understand the compliance landscape and can navigate it effectively.

Showcase Your Experience

Prepare specific examples from your past roles where you successfully implemented quality processes or contributed to regulatory submissions. Highlighting your hands-on experience will demonstrate your capability and readiness for the role.

Understand Risk Management

Brush up on risk management principles and how they apply to software quality in medical devices. Be ready to discuss how you've identified and mitigated risks in previous projects, as this is a key aspect of the role.

Passion for Patient Health

Express your enthusiasm for contributing to technologies that enhance patient health. Companies want to see that you’re not just qualified but also genuinely care about making a difference in the MedTech field.

Software Quality Engineer – MedTech & Regulatory
Lenntech Search

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