Senior System Verification Engineer

CMR Surgical; Cambridge; On-site; GBP 45,000 - 65,000; Full time

Benefits offered by this job

Competitive salary

Bonus

Pension

Healthcare

Enhanced parental leave pay

Job summary

CMR Surgical in Cambridge is seeking a Senior System Verification Engineer to support system level verification for new designs and formal verification activities. You'll define and execute test protocols, lead verification engineers, and ensure compliance with health and safety regulations.

The ideal candidate has a degree in Engineering or Physics, experience in testing, and strong problem-solving skills. A competitive salary and benefits package are offered, including bonuses and healthcare.

Qualifications

• Experience planning, executing, and reviewing testing in a regulated environment.
• Experience leading small technical teams.
• Familiarity with medical devices standards and certification.

Responsibilities

• Define and execute test protocols from system, user and risk related requirements.
• Review test related documentation and ensure it meets regulatory guidelines.
• Monitor and report test progress to the Group Lead or Head of Quality Engineering.

Skills

Problem solving

Attention to detail

Electromechanical skills

Technical leadership

Communication

Education

Degree in Engineering, Physics or other technical discipline

Tools

Python

Job description

About the Role

The Senior System Verification Engineer will support the delivery of system level verification for new system designs and formal verification activities for the full system.

The primary activities include creating test protocols from the system and sub‑system requirements, executing and reporting the protocol results to design teams and regulatory, and capturing and following through on any deviations or issues found during testing. The role includes assessing the impact of new requirements on the existing protocols as well as deriving suitable tests for new requirements (either manual or automated).

Responsibilities

• Definition and execution of test protocols from system, user and risk related requirements
• Reviewing of test related documentation (protocols, reports, memorandums, etc.)
• Supporting the creation of bespoke test environments and rigs (software, hardware or combination of both)
• Defining and documenting the impact on system level behaviour as a result of design changes, and ensuring this is fully verified.
• Developing process improvements to streamline test activities, including test script development (Python).
• Creating test plans and schedules for testing activities coming into the group.
• Task leading verification engineers to deliver projects.
• Monitoring and reporting test progress to the Group Lead or Head of Quality Engineering.
• Ensuring Verification documentation meets regulatory guidelines and standards (FDA / MDR / Other regions).
• Working with other areas of the business to ensure all health and safety, training records and equipment calibration processes are in compliance.

About you

To be successful in this role, you’ll need to have/be:

• Enthusiastic, curious, energetic and proactive – and interested in what CMR is seeking to achieve.
• Good problem solving skills with a keen interest in understanding how things work.

Alongside excellent electromechanical skills gained from your degree in Engineering, Physics or other technical discipline, we would like you to have:

• High attention to detail and excellent communication skills
• Experience planning, executing, and reviewing testing
• Experience leading small technical teams
• Experience with recruitment, appraisals, and line management
• Experience working in a regulated environment

Additional qualifications

• Robotics
• Familiarity with medical devices standards and certification

Why Join Us?

We offer a competitive salary and a great benefits package including a bonus, pension, healthcare and enhanced global parental leave pay.

This role requires candidates to have eligibility to work within the UK.