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- Tasks: Ensure software quality and compliance for innovative medical devices.
- Company: Join a pioneering R&D company revolutionising medical diagnostics.
- Benefits: Enjoy flexible working, 25 days’ holiday, and a pension scheme.
- Why this job: Make a significant impact in a fast-growing field with a passionate team.
- Qualifications: Experience in SDLC processes, software quality engineering, and ISO standards required.
- Other info: Opportunity to work on meaningful products that impact the medical field.
The predicted salary is between 36000 - 60000 £ per year.
Software Engineer, Quality, IEC 62304, ISO 13485, Medical Devices, COR7184 A rare and exciting opportunity has arisen for a Software Engineer with experience working with software as a medical devices and IEC 62304 standards, to join a pioneering scientific R&D company specialising in the development of medical devices. The Role The Software Engineer will take ownership of ensuring software quality and compliance for innovative In Vitro Diagnostic products. Working alongside a highly skilled team, you’ll be responsible for implementing and maintaining SDLC processes, software risk management, and compliance with ISO 13485, IEC 62304, and 21 CFR Part 820. This is a fantastic opportunity to make a significant impact in a fast-growing company at the forefront of medical technology. The Company The Software Engineer will join an innovative organisation leading the way in medical device development. This company is revolutionising diagnostics, and as they continue to grow, they are looking for a passionate Quality Engineer to enhance their software quality and risk management processes. Benefits Flexible working, including remote options 25 days’ holiday Pension scheme What’s Required of the Software Engineer? Experience defining, implementing, and maintaining Software Development Life Cycle (SDLC) processes Proven experience in software quality engineering and risk management Strong knowledge of ISO 13485, IEC 62304, 21 CFR Part 820, IVDR Experience in software security risk management (SW:96:2023, ISO 27001, IEC 80001) is a plus What Next? If you’re a Software Quality Engineer looking to work on meaningful products that will have a massive impact in the medical field, apply today to learn more! Software Engineer, Quality, IEC 62304, ISO 13485, Medical Devices Corriculo Ltd acts as an employment agency and an employment business. #INDITO #channelA #MR #J-18808-Ljbffr
Software Engineer, Quality, IEC 62304, ISO 13485, Medical Devices, COR7184 employer: Beautyk Creative
Contact Detail:
Beautyk Creative Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Software Engineer, Quality, IEC 62304, ISO 13485, Medical Devices, COR7184
✨Tip Number 1
Familiarise yourself with the specific standards mentioned in the job description, such as IEC 62304 and ISO 13485. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to quality in medical device software.
✨Tip Number 2
Network with professionals in the medical device industry, especially those who have experience with software quality engineering. Attend relevant conferences or webinars to make connections that could lead to valuable insights or referrals.
✨Tip Number 3
Prepare to discuss your previous experiences with SDLC processes and risk management in detail. Be ready to provide examples of how you've implemented these processes in past roles, as this will showcase your practical knowledge and problem-solving skills.
✨Tip Number 4
Research the company’s recent projects and innovations in the medical device field. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show genuine interest in contributing to their mission.
We think you need these skills to ace Software Engineer, Quality, IEC 62304, ISO 13485, Medical Devices, COR7184
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with software quality engineering, IEC 62304 standards, and ISO 13485 compliance. Use specific examples from your past roles to demonstrate your expertise in these areas.
Craft a Compelling Cover Letter: In your cover letter, express your passion for medical technology and how your skills align with the company's mission. Mention your experience with SDLC processes and risk management, and explain why you are excited about this opportunity.
Showcase Relevant Projects: If you have worked on any projects related to medical devices or software quality, be sure to include them in your application. Describe your role, the challenges faced, and the outcomes achieved to illustrate your capabilities.
Highlight Continuous Learning: Mention any relevant certifications or training you have completed, especially those related to ISO standards or software security risk management. This shows your commitment to staying updated in the field and enhances your application.
How to prepare for a job interview at Beautyk Creative
✨Understand the Standards
Make sure you have a solid grasp of IEC 62304 and ISO 13485. Be prepared to discuss how these standards apply to software development in medical devices, as this will demonstrate your expertise and commitment to quality.
✨Showcase Your SDLC Knowledge
Be ready to explain your experience with Software Development Life Cycle processes. Highlight specific examples where you've implemented or maintained these processes, as this is crucial for the role.
✨Discuss Risk Management Experience
Prepare to talk about your experience in software risk management. Share examples of how you've identified, assessed, and mitigated risks in previous projects, especially in the context of medical devices.
✨Express Your Passion for Medical Technology
Convey your enthusiasm for working in the medical field. Discuss why you are passionate about improving diagnostics and how you see your role contributing to meaningful advancements in healthcare.
