Verification & Validation Engineer

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology company dedicated to creating a future of better care. We embrace collaboration with our partners and patients and take pride in the pursuit of scientific excellence - with the goal of transforming medical technology as we know it. Because that’s how we change the lives of patients for the better. And that’s how we create better together.

As a key member of the Enabling Technologies team, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Job Description

We are seeking a detail-oriented and collaborative Verification & Validation (V&V) Engineer to support the verification and validation of software and system functionality for medical device products within Enovis' Enabling Technologies business. This role is responsible for ensuring software requirements, system designs, and user needs are thoroughly verified and validated through structured testing activities in compliance with medical device quality and regulatory standards.

The V&V Engineer will partner closely with Software Engineering, Systems Engineering, Product Development, Quality, Regulatory Affairs, and Program Management teams to develop test strategies, execute verification and validation activities, document results, and support successful product releases. This position requires strong analytical thinking, technical problem-solving skills, and the ability to work effectively within an Agile software development environment.

The ideal candidate is a proactive team player with excellent technical writing and communication skills who is passionate about delivering high-quality, reliable medical device software.

Key Responsibilities:

• Develop, execute, and maintain verification and validation test plans, protocols, and reports for software and system-level requirements.

• Review product requirements, software specifications, and design documentation to develop comprehensive test cases and validation strategies.

• Perform hands-on software verification and validation testing for new product development and enhancements to existing products.

• Document test results, identify defects, and work closely with development teams to investigate, troubleshoot, and verify software issues.

• Review software documentation and participate in quality audits to ensure compliance with applicable medical device standards and company procedures.

• Participate in Agile ceremonies, including daily stand-ups, sprint planning, backlog refinement, and retrospectives, providing updates on testing activities.

• Track testing progress, maintain defect logs, and communicate project status, risks, and issues to engineering leadership.

• Collaborate with cross-functional teams to ensure verification and validation activities support project timelines and product release objectives.

• Assist with test planning, test automation initiatives, and continuous improvement of V&V processes and documentation.

• Support regulatory submissions and quality system activities by providing verification and validation documentation as required.

Required Qualifications:

• Bachelor’s degree in Biomedical Engineering, Software Engineering, Computer Engineering, Electrical Engineering, Computer Science, or a related engineering discipline.

• Minimum 2–3 years’ experience in software verification and validation, software quality assurance, or medical device development.

• Experience working within regulated industries, preferably medical devices.

• Knowledge of the software development lifecycle (SDLC) and software verification and validation methodologies. 

• Experience developing test plans, test protocols, test cases and verification reports. 

• Strong technical writing, analytical and organisational skills.

• Excellent written and verbal communication skills, with the ability to work effectively across cross-functional teams.

Skills & Experience:

• Experience working in Agile software development environments.

• Familiarity with Australian medical device regulatory requirements, including TGA requirements, as well as relevant international standards such as ISO 13485, IEC 62304 and FDA requirements.

• Understanding of software architecture concepts and design patterns.

• Experience using defect tracking, test management and requirements management tools.

• Basic debugging skills, including reviewing application logs and troubleshooting software issues.

• Understanding of musculoskeletal anatomy and orthopaedic medical devices is desirable.

• Experience supporting software verification and validation for medical device products.

At Enovis, we’re focused on Creating Better Together!
We’re proud to share that Enovis™ Healthcare Solutions has been recognized as a winner in the 2026 TAG Awards for MedTech, an industry program produced by The Aebli Group. This year’s awards celebrate organizations that are pushing the boundaries of innovation across MedTech, Life Sciences, and BioTech - turning bold ideas into real-world impact.

We embrace diversity, equity, and inclusion and are committed to creating a respectful and inclusive workplace where everyone belongs.

Learn more about us:
🌐 https://ourpurpose.enovis.com/
🌐 https://enovis.com