Jobid=634363093755174664 (0.034)
Do you want to be part of one of the TOP Healthcare company in the world ?
We are seeking a detail-oriented and proactive Quality Engineer to join our team of Manufacturing.
Contract: Contract worker until April 27, with possibility to stay long term in the company after performance review.
Salary range: (NON NEGOTIABLE) 3800 – 4800/ gross (excluding holiday allowance)
NO RELOCATORS
Responsibilities
- Manage and support core quality processes, including nonconformance management, CAPAs, complaint investigations, DHR reviews, and quality governance activities.
- Provide daily manufacturing quality support on the shop floor through Gemba walks, Tier meetings, Kaizen activities, and production issue resolution.
- Investigate component and material quality issues, ensuring proper containment, documentation, disposition, and escalation.
- Drive First Time Quality (FTQ) initiatives and support Operational Quality Walks to improve quality performance.
- Analyze quality metrics and KPIs to identify trends, root causes, risks, and improvement opportunities.
- Support change control activities and maintain compliance within the site's Quality Management System (QMS).
- Coordinate quality improvement projects, ensuring milestone achievement, progress tracking, and stakeholder alignment.
- Support risk management activities, including assessments, mitigation plans, and action tracking.
- Prepare for internal and external audits, providing documentation, evidence, and follow-up support.
- Lead continuous improvement initiatives to enhance manufacturing processes, reduce inspection burden, and improve overall quality performance.
Requirements
- Bachelor's degree with 4+ years of relevant experience, or a Master's degree with 2+ years of relevant experience in Manufacturing Quality, Quality Engineering, Industrial Engineering, or a related technical field.
- Strong experience with CAPA management, investigations, nonconformances, and complaint handling.
- Solid understanding of Quality Management Systems (QMS), document control, and change control processes.
- Hands-on experience supporting manufacturing operations from raw materials through finished product.
- Background working within a highly regulated industry, ideally Medical Devices, Pharmaceuticals, or Life science
- Fluent English required; Dutch language skills are highly preferred
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