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.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975.

Before submitting your CV, please take a moment to check the layout, spelling, and grammar. If your CV includes graphics or design features, we'd also appreciate a simplified version in Word format.

If this role isn't for you, please check out our website for other roles that may be suitable, or send us your CV, we would still like to hear from you! You can find us on our website or LinkedIn, Facebook, Instagram and x@nagrecruitment

We are committed to fostering a diverse and inclusive environment in line with the Equality Act 2010. All qualified applicants will be considered regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. New Appointments Group acts as an Employment Agency for permanent roles and as an Employment Business for temporary roles.