Quality Systems Engineer

JobsCloseBy Editorial Insights

AROA Biosurgery Limited is seeking a Quality Systems Engineer for a 9-month fixed-term, onsite in Auckland, to maintain the QMS, support audits and regulatory inspections, manage supplier qualification and quality issues, oversee complaint handling and CAPA, and drive continuous improvement through quality metrics while partnering across functions; this role covers parental leave. The role requires a degree in engineering, quality or related discipline and 3+ years in a regulated environment (ideally medical devices), with hands-on experience in QMS, audits, supplier quality, CAPA, and regulatory requirements, plus strong communication and project management. To apply, tailor your resume and cover letter to highlight CAPA outcomes, audit readiness, cross-functional collaboration, NZ working rights, and your fit for a mission-led team, noting availability for fixed-term work and comfort with onsite collaboration and flexible options.

At AROA, our people come to work every day with passion and ideas that fuel our business and go home knowing they have made a real difference in the lives of others.

AROA, which is Maori for ‘understanding’, is proudly New Zealand born and based. We develop, manufacture, and export innovative wound care products, improving the lives of millions around the world by unlocking extraordinary outcomes for our patients. Our mission is to be the global leader in regenerative healing, making our products and services accessible to everybody. 

About the role

We’re looking for an experienced Quality Systems Engineer to play a key role in maintaining AROA’s Quality Management System. Partnering closely with teams across the business, you’ll provide guidance on regulatory compliance, audits, supplier quality, complaint handling, and CAPA. This is a 9-month fixed-term role covering parental leave.

Key responsibilities

• Maintain the Quality Management System (QMS), ensuring compliance with regulatory and quality standards
• Support external audits and regulatory inspections
• Manage supplier qualification, monitoring, performance, and complex supplier quality issues
• Oversee complaint handling processes, including investigations, trend analysis, root cause identification, and corrective/preventive actions
• Facilitate and drive the CAPA process, ensuring effectiveness and continuous improvement
• Develop and use quality metrics to identify trends and improvement opportunities
• Provide QMS training and act as a key quality partner across cross-functional teams

What you’ll bring
You’ll have a degree in engineering, quality, or a related discipline, along with 3+ years’ experience in a quality role within a regulated (ideally medical device) environment. You’ll bring hands-on experience with QMS, audits, supplier quality, CAPA, and complaint handling, and a solid understanding of regulatory requirements.

You’re confident representing quality in audits and inspections, comfortable working through complex problems, and able to translate regulatory requirements into
practical, value adding solutions. Strong communication, analytical thinking, and project management skills will be key to success in this role.

What we offer:

At AROA NZ, we value our people and make sure working with us is rewarding, both professionally and personally. Here’s what you can enjoy as part of our team:

• Convenient Location – Free carparking onsite at our Airport Oaks sites with easy motorway access.
• Sustainable Travel Support – Fareshare public transport subsidy, WorkRide program, onsite bike shed, and electric bike charging stations.
• Flexible/Hybrid Work Options – Where roles permit, enjoy flexibility to balance work and life.
• Career Growth & Impact – Be part of a mission-led company doing work that’s never been done before, with opportunities for learning, development, and real impact.

To be considered for this opportunity you must have existing NZ working rights.