Senior Quality Engineer

Our client, a leading MedTech startup, is seeking an experienced Senior Quality Engineer to drive quality initiatives and ensure compliance with ISO 13485:2016. This role focuses on CAPA management, risk assessment, supplier quality, and design control activities.

Key Responsibilities:

• Lead Corrective and Preventive Action (CAPA) and Nonconformance Management.
• Support design control activities and risk analysis (FMEA).
• Conduct Design Verification and Validation (V&V).
• Maintain and improve Quality Management System (QMS).
• Prepare and present quality metrics.

About You:

We’re looking for a detail-oriented professional with experience in regulated industries. While medical device experience is preferred, candidates from other regulated sectors are encouraged to apply.

Skills & Experience:

• Bachelor’s degree in Science, Engineering, or Technology.
• Experience in a senior quality position (med device or pharma preferred). 
• Strong knowledge of ISO 13485:2016.
• Experience with QMS processes, risk management, CAPA, and nonconformance management.
• Excellent technical writing and problem-solving skills.
• Understanding of software development lifecycle (no coding required).

Why Apply?

• Competitive salary that reflects your seniority
• Hybrid work model – 2 days in the Newmarket office.
• Join a well-funded, innovative startup with a collaborative team culture.

How to apply

Click APPLY NOW or call Belinda on 09 200 3121 for a confidential discussion.  
To apply for this vacancy you MUST be a New Zealand citizen, or resident, or have already secured the right to work in New Zealand and therefore hold a valid visa.

Scitex specialises in permanent, contract and temporary recruitment – and has done so since 1987. We are here to engineer better Mondays. We love connecting talented people with great work opportunities in workplaces where you can thrive and make a meaningful difference.