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For Companies At a Glance
- Tasks: Ensure software compliance, lead risk management, and oversee quality processes in a dynamic team.
- Company: Illumina is revolutionising health equity through genomic technology for billions worldwide.
- Benefits: Enjoy flexible time off, private medical insurance, and a stock purchasing programme.
- Why this job: Make a real impact on human health while working with inspiring leaders and innovative projects.
- Qualifications: B.S./M.S. in engineering or related field with extensive Quality Engineering experience in medical devices.
- Other info: Remote work available from the UK, Spain, or Italy; no visa sponsorship offered.
The predicted salary is between 42000 - 84000 £ per year.
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What if the work you did every day could impact the lives of people you know? Or all of humanity?
At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.
Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.
Senior Software Design Quality Engineer
Ideal candidate will work remotely from the United Kingdom, Spain, or Italy.
Note- This is NOT a Software Testing position.
As a Senior Software Design Quality Engineer at Illumina, you will ensure compliance of IVDR and RUO software with regulations, lead risk management activities, and oversee software quality processes. You will collaborate with cross-functional teams to drive best practices, software security, and risk mitigation throughout the product lifecycle.
Why Us?
What if the work you did every day could impact the lives of people you know? Or all of humanity?
At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.
Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.
Illumina\’s employee benefits are industry-leading and include flexible time off, private medical insurance, compassion and care time off, leisure travel insurance, pension, employee stock purchasing program, volunteer time off, and much more!
Responsibilities
- Provide technical and strategic feedback associated with IVDR software as well as RUO software and digital health aligned with applicable regulations, standards, and business needs.
- Lead the development and maintenance of the Risk Management File (RMF) including risk management plans, hazards analysis, dFMEAs, pFMEAs, and risk management report.
- Provide Quality Engineering input, review, and approval of the Design History File (DHF) and associated documentation. Responsible for quality oversight and approval of software product development plans, design inputs and outputs, verification and validation, and review of test planning, protocols, and reports.
- Serve as the SME for software quality and collaborate with teams on code reviews, software security analysis, defect and vulnerability triage, creation and maintenance of sBOMs, etc., and lead implementation of best practices for software quality processes.
- Participate in design reviews to ensure the effective development, transfer, and maintenance of the product throughout the product lifecycle.
- Establish and cultivate positive relationships with cross-functional stakeholders and product development team members to optimize the success of development projects.
- Support other areas of the Quality System and perform other tasks as defined by Management.
Required Skills And Experience
- B.S./M.S. in relevant engineering field (e.g., biomedical, computer science, software, electrical, etc.) or equivalent scientific degree.
- Many years of progressive Quality Engineering experience in the medical device industry with hands-on support for software development.
- Strong solid understanding of international medical device/IVDR regulations and standards, including 21 CFR 820, ISO 13485, IEC 62304, and ISO14971.
- Solid understanding of software developmental best practices for digital health software, Medical Device Data Systems, and cloud-based software/systems.
- Organized self-starter, able to work in a fast-paced environment.
- Ability to work independently and as part of team, strong collaborative skills.
- Preferred skills and experience:
- Understanding of Artificial Intelligence, data management and related regulations/standards requirements.
- Experience working within an AAMI TIR45 framework/ Agile software development for the development of SaMD/Digital health.
- Experience supporting development of cloud-based software and understanding of cloud infrastructure and deployment.
- What can you expect?
Our team members are bright, energetic, and dedicated – they are the driving force behind our innovation and impact. To attract the best and brightest, we offer a competitive employee benefits program. We view it as a smart investment in our people, one that recognizes the tremendous value they bring to our business every day. At Illumina, we push boundaries. We think beyond the conventional. We dream big. With the energy of so many bright and accomplished people, the opportunities are endless.
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact To learn more, visit: The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.
Seniority level
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Seniority level
Not Applicable
Employment type
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Employment type
Full-time
Job function
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Job function
Engineering and Information Technology
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Industries
Biotechnology Research, Research Services, and Medical Equipment Manufacturing
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Sr. Software Design Quality Engineer employer: Illumina
Contact Detail:
Illumina Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr. Software Design Quality Engineer
✨Tip Number 1
Familiarise yourself with the specific regulations and standards mentioned in the job description, such as IVDR, ISO 13485, and IEC 62304. Being able to discuss these in detail during your interview will demonstrate your expertise and commitment to quality engineering in the medical device industry.
✨Tip Number 2
Network with professionals in the medical device field, especially those who have experience with software quality processes. Engaging in conversations about best practices and challenges can provide you with valuable insights that you can bring up during your interview.
✨Tip Number 3
Prepare to showcase your experience with risk management activities and how you've successfully led similar projects in the past. Be ready to share specific examples of how you’ve contributed to software quality oversight and compliance in previous roles.
✨Tip Number 4
Research Illumina’s recent projects and initiatives in genomic technology. Understanding their mission and how your role as a Senior Software Design Quality Engineer fits into their goals will help you articulate your passion for the position and the company during the interview.
We think you need these skills to ace Sr. Software Design Quality Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in Quality Engineering, particularly in the medical device industry. Emphasise your understanding of IVDR regulations and any specific software quality processes you've led.
Craft a Compelling Cover Letter: In your cover letter, express your passion for genomic technology and how your skills align with Illumina's mission. Mention specific projects or experiences that demonstrate your ability to lead risk management activities and collaborate with cross-functional teams.
Showcase Relevant Skills: Clearly outline your technical skills related to software development best practices, risk management, and compliance with international standards. Highlight any experience with Agile methodologies or cloud-based software development.
Proofread and Edit: Before submitting your application, thoroughly proofread your documents for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role focused on quality assurance.
How to prepare for a job interview at Illumina
✨Understand the Regulatory Landscape
Familiarise yourself with IVDR and RUO software regulations, as well as international standards like ISO 13485 and IEC 62304. Being able to discuss these in detail will show your expertise and readiness for the role.
✨Showcase Your Quality Engineering Experience
Prepare to discuss your previous experience in Quality Engineering, particularly in the medical device industry. Highlight specific projects where you led risk management activities or contributed to software quality processes.
✨Demonstrate Collaboration Skills
Since this role involves working with cross-functional teams, be ready to share examples of how you've successfully collaborated with others in past roles. Emphasise your ability to build positive relationships and drive best practices.
✨Prepare for Technical Questions
Expect technical questions related to software development best practices and risk management. Brush up on your knowledge of software security analysis and defect triage, as these are crucial aspects of the role.
