Senior System Verification Engineer

CMR Surgical Ltd.; Town of Cambridge; Sur place; AUD 144 000 - 182 000; Plein temps

Avantages offerts par ce poste

Bonus

Pension

Healthcare

Résumé du poste

CMR Surgical is seeking a Senior System Verification Engineer to drive system-level verification for new designs and formal verification activities. The role focuses on creating and executing test protocols, evaluating results, and ensuring regulatory compliance across FDA, MDR and other regions.

The position is based on-site at Cambridge premises, with responsibilities including test planning, process improvements, and leading verification engineers to deliver projects within a fast-growing,

Qualifications

• Degree in Engineering, Physics or related technical discipline.
• Experience planning, executing and reviewing testing.
• Experience leading small technical teams.
• Experience in a regulated environment.
• Strong problem-solving and communication skills.

Responsabilités

• Definition and execution of test protocols from system, user and risk requirements.
• Reviewing test documentation (protocols, reports, etc.).
• Supporting bespoke test environments and rigs (software/hardware).
• Documenting impact on system behavior due to design changes and ensure full verification.
• Developing test scripts (Python) and related tooling.
• Creating test plans and schedules for testing activities.
• Leading verification engineers to deliver projects.
• Reporting test progress to Group Lead/Head of Quality Engineering.

Connaissances

Test protocol development

Python scripting

Regulatory knowledge

Electromechanical skills

Leadership

Communication

Formation

Engineering, Physics or related degree

Outils

Python

Description du poste

AtCMR Surgical, we're revolutionising the future of minimal access surgery withVersius, our next-generation surgical robotic system. We're growing fast, and we’re on a mission to transform how surgery is delivered globally for the benefit of patients, clinicians, and healthcare systems.

Our values—Ambitious, Humble, People-Focused, and Fair & Responsibledefine our approach to innovation, partnership, and growth. If you believe in making a meaningful difference in healthcare and want to be part of a purpose-driven company with bold ambitions, now is the time to join us.

CMR is an exciting and evolving company to be joining right now. Our commitment to our goal of building a world-class medical devices company is underpinned by the ground-breaking innovation of our next generation of surgical robots and a diverse team of talented and supportive individuals.

We’re breaking new ground which makes working here exciting, it provides autonomy, opportunity and makes the things you do visible. Come and join us and see what you’re capable of.

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 being able to assess the impact of new requirements on the existing protocols as well as being able to derive suitable tests for new requirements (either manual or automated).

This role is based on-site at our Cambridge premises.

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.

We’d expect you to be willing to turn your hand to anything within the System Verification remit that helps the team deliver its objectives.

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

In addition, any experience of the following would be advantageous:

• Robotics
• Familiarity with medical devices standards and certification

At CMR we’re building a diverse, inclusive, and authentic workplace; what matters most to us is that you identify with our values and are passionate about making a difference.

Why Join Us?

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

Interested? We’d love to hear from you!

This role requires candidates to have eligibility to work within theUK.
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