At a Glance
- Tasks: Lead quality and compliance for innovative products across Europe & Africa.
- Company: A leading multinational manufacturer with a commitment to quality.
- Benefits: Competitive salary, diverse work environment, and opportunities for professional growth.
- Other info: Join a dynamic team and influence cross-functional initiatives.
- Why this job: Make a real impact in a global business while ensuring high product standards.
- Qualifications: 8+ years in quality roles, strong knowledge of regulatory compliance.
The predicted salary is between 60000 - 80000 £ per year.
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.
Quality Lead in Maidstone employer: New Appointments Group
As a leading multinational manufacturer, we pride ourselves on being an excellent employer that values quality and compliance across our Europe & Africa operations. Our collaborative work culture fosters innovation and professional growth, offering employees the chance to influence high-quality product launches while working alongside diverse teams. With a commitment to regulatory excellence and continuous improvement, we provide unique opportunities for career advancement in a dynamic and supportive environment.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Lead in Maidstone
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that Quality Lead role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of MDD/MDR, ISO 13485, and other key regulations. We recommend practising common interview questions and scenarios related to quality management systems. Show them you’re the expert they need!
✨Tip Number 3
Don’t forget to showcase your hands-on experience! When discussing your past roles, highlight specific projects where you led quality assessments or audits. We want to see how you’ve made an impact in previous positions.
✨Tip Number 4
Finally, apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we have loads of other roles that might catch your eye if this one isn’t quite right for you.
We think you need these skills to ace Quality Lead in Maidstone
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Lead role. Highlight your experience with regulatory compliance and quality management systems, as these are key for us. Use specific examples that showcase your expertise in MDD/MDR and ISO 13485.
Showcase Your Skills:Don’t just list your skills; demonstrate them! Use your application to show how you've influenced cross-functional teams or led quality projects. We want to see your hands-on experience and strategic thinking in action.
Keep It Professional:Before hitting send, double-check your application for any spelling or grammar mistakes. A polished application reflects your attention to detail, which is crucial in a quality role like this one. Remember, we appreciate a clean layout too!
Apply Through Our Website:We encourage you to apply through our website for the best chance of being noticed. If this role isn’t quite right for you, don’t hesitate to send us your CV anyway. We’re always on the lookout for talented individuals to join our team!
How to prepare for a job interview at New Appointments Group
✨Know Your Regulations
Make sure you brush up on the key regulations like MDD/MDR, ISO 13485, and MHRA. Being able to discuss these confidently will show that you’re not just familiar with the standards but can also apply them in real-world scenarios.
✨Showcase Your Technical Expertise
Prepare to discuss your hands-on experience with quality methods and statistical analysis. Bring examples of how you've implemented quality plans or led audits in previous roles to demonstrate your capability.
✨Communicate Effectively
Practice articulating your thoughts clearly, especially when discussing complex topics. Remember, you’ll need to influence senior stakeholders, so being concise and persuasive is key.
✨Demonstrate Project Management Skills
Be ready to talk about how you’ve managed multiple projects and priorities in the past. Highlight specific instances where you balanced strategic planning with execution to achieve operational goals.
