The role is within the Global Sustainability and Supply Chain Services, leading the innovation, development, and maintenance of key resources within the Circularity pillar to enable the adoption of Circularity and Sustainability Certification products. The Global Circularity and Sustainability Certification Manager is a key pillar of the Global Sustainability strategy and responsible for the development and maintenance of Circularity products and guidance within the network, reporting to the Global ESG Assurance, Climate and Circularity Manager.
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Join Strykerβs Design Quality Digital team as a Principal Design Quality Engineer and help shape the future of digital solutions. In this role, youβll influence product development from concept to launch, ensuring patient safety, product security, and compliance with global standards. Your expertise will drive innovation and quality in life-changing medical technologies.
Oversee the quality oversight of design controls and risk management of the combination product projects from inception through commercialization. This role involves collaboration with cross-functional teams and external partners to ensure that combination products meet regulatory standards, and are safe and effective for patient use.
As a Regional Health, Safety & Wellbeing (HSW) Advisor - Construction, youβll be the go-to expert for HSW across multiple construction sites in the South Island. Youβll work closely with Project Managers, Site Managers, and contractors to ensure compliance, drive continuous improvement, and foster a culture of safety and wellbeing.
Join the Health and Safety consultancy department as our new Health & Safety Consultant, delivering a wide range of strategic and operational risk management assignments. You will be delivering health and safety risk management services in a multi-disciplinary project environment and working closely with a wide range of clients to develop proposals for new client work.
Seeking a proactive, hands-on Quality Manager to build, lead, and continuously improve our Quality Management System (QMS). This role is ideal for a quality professional who thrives in a fast-paced, early-stage environment and wants to directly influence product development, regulatory readiness, and company culture. Responsible for maintaining compliance with FDA 21 CFR Part 820 and ISO 14971, while also supporting design control, supplier qualification, risk management, and post-market processes.