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KARL STORZ is seeking a Senior Biomedical Engineer NZ to lead the NZ workshop operations in Sandringham. You will manage equipment intake, ensure accurate service records in SAP and QMS, and perform inspections and repairs of capital medical equipment.
Role emphasises asset lifecycle management, regulatory compliance (ANZ 3551, Medsafe, TGA), software updates, and strong fault diagnosis. On-site role with hybrid flexibility in NZ.
Senior Biomedical Engineer NZ (m/f/d) at KARL STORZ in Sandringham, N, NZ. This Full time on site position offers great opportunities for career growth. Job Function: Repair & Service Location: Auckland, NZ, 1025 Work Location (for field-based positions): Work Flexibility: Hybrid Job ID: 5904
Oversee the day-to-day operations of the New Zealand workshop, including equipment intake, job prioritisation, and maintaining an organised and efficient workspace. Maintain accurate and up-to-date service records, job tracking, and work orders within SAP and the KARL STORZ Quality Management System (QMS), ensuring all documentation is audit-ready at all times. Inspect, test, and repair loan and demonstration equipment to ensure availability meets the needs of the sales and customer teams. Drive a proactive and strategic approach to asset lifecycle management by identifying aging equipment, prioritising service or replacement needs, and aligning actions with customer requirements and service contract commitments. Conduct safety and performance testing of KARL STORZ equipment in compliance with applicable regulatory standards, including ANZ 3551, and internal company requirements. Deliver both preventative maintenance and responsive repair services across the New Zealand customer base to ensure optimal equipment performance and reliability. Diagnose and resolve complex technical issues independently, escalating where necessary to ensure timely and effective resolution. Install and validate software updates, manage system integrations, and troubleshoot related issues to maintain and enhance overall equipment functionality and performance. Ensure all work is carried out in full compliance with Medsafe and TGA regulatory requirements, as well as applicable New Zealand health and safety legislation. Adhere to KARL STORZ quality standards and internal Quality Management System (QMS) requirements at all times. Apply sound knowledge of hospital and surgical environments, including relevant standards such as AS/NZS 3551 and AS/NZS 3200. Demonstrate working knowledge of ISO 13485 and its application within medical device servicing and quality processes. Support the continuous improvement of customer excellence processes, documentation, and quality standards in line with direction from the Biomedical Technology Manager.