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For Companies At a Glance
- Tasks: Lead verification of complex medical systems, ensuring they meet performance and regulatory standards.
- Company: Join a pioneering company dedicated to enhancing medical device quality and reliability.
- Benefits: Enjoy a 12-month contract with opportunities for professional growth and collaboration.
- Why this job: Make a real impact in healthcare while working with innovative technologies and talented teams.
- Qualifications: Bachelor's or Master's in Engineering with 5-10 years in system verification required.
- Other info: Remote work options may be available; perfect for tech-savvy problem solvers!
The predicted salary is between 36000 - 60000 £ per year.
As a Lead System Verification Engineer, you will be responsible for ensuring that complex systems meet their intended functionality and performance criteria, thereby contributing significantly to the overall quality and reliability of the medical device product.
Job Specification
- Planning and Performing Verification
- Develop and execute verification plans, protocols, and reports.
- Ensure all system verification activities comply with regulatory standards (e.g., FDA, ISO 13485, IEC 62304).
- Conduct risk analysis and ensure risk management activities are current and comprehensive.
- Developing Test Procedures
- Design and develop test cases and procedures based on system requirements and design specifications.
- Implement automated testing where applicable to enhance efficiency and repeatability.
- Analysing Data and Reporting Results
- Analyse test data and report on verification outcomes.
- Identify and document any defects or non-conformance, and collaborate with development teams to resolve issues.
- Working Collaboratively
- Work closely with cross-functional teams including design, firmware, and software engineers.
- Provide technical guidance and mentorship to junior verification engineers.
- Communicate verification progress and issues to stakeholders effectively.
- Maintaining Documentation
- Keep thorough records of all verification activities and results.
- Ensure traceability of verification activities to requirements and risk management documentation.
Education
A Bachelor's or Master's degree in Engineering (Biomedical, Electrical, Mechanical, Software, or a related field).
Experience
5-10 years of experience in system verification or a related field. Familiarity with regulatory standards and guidelines relevant to medical devices.
Knowledge, Skills, and Abilities
- Strong analytical and problem-solving skills.
- Ability to troubleshoot software and hardware issues.
- Proficiency in using verification and testing tools is a plus.
- Excellent written and verbal communication skills.
- Ability to work effectively in a collaborative team environment.
System Verification Engineer employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land System Verification Engineer
✨Tip Number 1
Familiarise yourself with the specific regulatory standards mentioned in the job description, such as FDA and ISO 13485. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to compliance in system verification.
✨Tip Number 2
Brush up on your experience with automated testing tools. Since implementing automated testing is highlighted in the role, showcasing your proficiency in this area during discussions can set you apart from other candidates.
✨Tip Number 3
Prepare examples of how you've collaborated with cross-functional teams in the past. Being able to articulate your experience in working closely with design, firmware, and software engineers will show that you can thrive in a collaborative environment.
✨Tip Number 4
Think about how you can demonstrate your analytical and problem-solving skills. Prepare to discuss specific instances where you've successfully identified defects or non-conformance and how you worked with teams to resolve these issues.
We think you need these skills to ace System Verification Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in system verification, particularly in the medical device sector. Emphasise your familiarity with regulatory standards like FDA and ISO 13485, as well as any specific tools you've used.
Craft a Compelling Cover Letter: In your cover letter, explain why you are passionate about system verification in medical devices. Mention specific projects or experiences that demonstrate your ability to develop verification plans and collaborate with cross-functional teams.
Showcase Your Analytical Skills: Provide examples in your application that showcase your strong analytical and problem-solving skills. Discuss how you've successfully identified defects or non-conformance in past roles and how you resolved these issues.
Highlight Team Collaboration: Since the role involves working closely with various teams, include examples of how you've effectively communicated and collaborated with engineers from different disciplines. This will show your ability to work in a collaborative environment.
How to prepare for a job interview at EPM Scientific
✨Know Your Regulatory Standards
Familiarise yourself with key regulatory standards such as FDA, ISO 13485, and IEC 62304. Be prepared to discuss how you have ensured compliance in your previous roles, as this is crucial for a System Verification Engineer.
✨Demonstrate Your Analytical Skills
Prepare examples that showcase your strong analytical and problem-solving skills. Discuss specific instances where you identified defects or non-conformance and how you collaborated with teams to resolve these issues.
✨Highlight Your Collaborative Experience
Emphasise your experience working with cross-functional teams. Share stories that illustrate your ability to communicate effectively with design, firmware, and software engineers, as well as how you’ve provided mentorship to junior engineers.
✨Showcase Your Documentation Skills
Be ready to talk about your approach to maintaining thorough records of verification activities. Discuss how you ensure traceability of verification activities to requirements and risk management documentation, as this is vital for the role.
