Quality Lead

Business & Product Quality Lead

A leading multinational manufacturer is seeking an experienced Business & Product Quality Lead to oversee quality and compliance across their Europe & Africa operations. This is a senior, technical role with responsibility for ensuring regulatory compliance and high product standards across new product launches and product changes.

The Role

Reporting to the GMG CoE - Quality Head, you will act as the technical expert on quality standards and regulatory requirements, including MDD/MDR, MHRA, ISO 13485, and QSR. You will collaborate closely with commercial, R&D, regulatory, manufacturing, and operations teams to deliver on-time, high-quality product launches.

This is a role for someone who combines strategic thinking with hands-on quality expertise, influencing cross-functional teams and leading the development and maintenance of the local Quality Management System (QMS).

Key Responsibilities

• Provide oversight of the QMS for all business products and services, ensuring regulatory compliance and adherence to corporate quality policies.
• Lead quality assessments and audits, acting as lead auditor for regulatory and internal inspections.
• Investigate product-related complaints and implement corrective and preventative actions using root cause analysis.
• Support new product introductions and product changes by developing quality plans and change control documentation.
• Monitor quality metrics, identify areas for improvement, and implement process enhancements.
• Train and guide colleagues in quality standards, methods, and compliance requirements.
• Manage multiple projects and priorities, ensuring strategic and operational goals are achieved.

Skills & Attributes

• Strong technical knowledge of quality methods, statistical analysis, process capability, sampling, and testing principles.
• Experience in regulatory compliance for medical devices and/or consumer products.
• Excellent communication skills with the ability to influence senior stakeholders.
• Strong project and resource management experience, with the ability to lead cross-functional initiatives.

• Ability to balance strategic planning with hands-on execution and problem-solving.

Education & Experience

• University degree in Engineering, Quality, Science, or a related discipline.
• 8+ years of technical experience in quality roles, ideally spanning consumer products and medical devices.
• Demonstrable knowledge of MDD/MDR, ISO 13485, MHRA, and medical device risk management.
• Track record of successfully managing quality projects, audits, and compliance activities across multiple functions.

This is an excellent opportunity for a senior quality professional to make a real impact in a global, multi-regional business.

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