Benefits Join a global medical technology company developing innovative solutions to improve patient outcomes Work across software and system verification and validation within medical devices Opportunity to work within a fast-paced agile product development environment About the company This global medical technology organisation is focused on advancing patient care through creative technologies and high-quality medical device solutions.
About the opportunity An exciting opportunity is available for a V V Engineer to join an established team based in Brisbane.
Working across software and system development projects, you will be responsible for supporting verification and validation activities throughout the product development lifecycle.
You will work closely with cross-functional engineering, quality and regulatory teams to ensure software requirements, system designs and user needs are effectively verified and validated.
This is an excellent opportunity for an engineer with 2–3+ years of experience who enjoys hands-on testing, technical problem solving and working within a regulated product development environment.
Duties Develop, execute and maintain software and system V V test plans, protocols and reports Review product requirements, software specifications and design documentation to develop comprehensive test cases Perform hands-on software verification and validation testing across new products and product enhancements Document test results, identify defects and work with development teams to investigate and troubleshoot software issues Track testing progress, defects, risks and issues throughout the development lifecycle Collaborate with Software Engineering, Systems Engineering, Quality, Regulatory Affairs and Product Development teams Support test planning,



test automation initiatives and continuous improvement activities Review software documentation and contribute to quality and compliance activities Support regulatory submissions through the preparation and provision of V V documentation Skills and Experience Tertiary qualification in Biomedical Engineering, Software Engineering, Computer Engineering, Electrical Engineering, Computer Science or a related discipline 2–3+ years of experience in software verification and validation, software quality assurance or medical device development Experience working within a regulated industry, ideally medical devices Understanding of software development lifecycle and software V V methodologies Experience developing test plans, protocols, test cases and verification reports Strong technical writing and documentation skills Strong analytical and problem-solving capability Experience working with cross-functional technical teams Culture Join a collaborative and quality-focused environment where engineering, quality, regulatory and product teams work closely together.
How to Apply Ready to take the next step?
Click apply or contact Gemma Staddon on ****** for a confidential discussion.
About Healthcare Professionals Group Healthcare Professionals Group recruits all positions: executive, permanent, contracting/temp, at all levels, across all areas of healthcare - Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care.
Medical Affairs Life Sciences Recruitment - Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific; Commercial Recruitment - Marketing, Sales, Analytics, Government and External Affairs; Business Operations Infrastructure Recruitment - Administration, Customer Service, Engineering, Finance, Human Resources, IT, L D, Legal, Manufacturing, Operations, Supply Chain, Warehouse; Clinical Care Recruitment - Allied Health, Aged Care, General Practice, Medical Imaging, Medical Management, Medical Specialties, Nursing.

📌 Verification & Validation Engineer (Queensland)
🏢 Healthcare Professionals Group
📍 Queensland