At a Glance
- Tasks: Ensure top-notch quality standards across products and processes while supporting audits.
- Company: Join a mission-driven company dedicated to food safety and quality.
- Benefits: Standard benefits package with opportunities for skill development in quality management.
- Why this job: Make a real impact on food safety and quality while growing your career.
- Qualifications: Relevant experience or qualifications in scientific or technical fields preferred but not essential.
- Other info: Dynamic work environment with recognition for your contributions to quality.
The predicted salary is between 30000 - 40000 £ per year.
It's fun to work in a company where people truly believe in what they are doing! Join us as a Quality Engineer and play a key role in maintaining and enhancing our quality standards across products, processes and systems. This position is suited to someone with strong attention to detail and a structured approach, who is ready to take responsibility for core Quality Management System (QMS) activities and support regulatory and client audits. You will work closely with colleagues across the organisation to ensure all quality activities meet our regulatory, health & safety, legal and environmental requirements.
Responsibilities
- Perform and maintain core site QMS activities, including CAPAs, investigations, complaints and change controls.
- Ensure corrective actions are implemented for non-conformances and carry out effective verification of these actions.
- Conduct detailed root cause analyses and identify opportunities for continuous improvement.
- Perform internal process audits in line with the audit schedule and contribute to audit reporting and follow-up actions.
- Maintain and report monthly KPIs from the electronic QMS, including detailed trend analysis of non-conformities.
- Oversee final product release, including review and approval of data, certificates of analysis (CoAs) and product labelling, ensuring compliance with applicable standards.
- Support the maintenance of ISO 9001, ISO 13485 and ISO 17025 certifications, and assist in the preparation and facilitation of client and regulatory audits.
Qualifications
- Relevant scientific qualification (e.g. in a scientific, technical or engineering discipline) is desirable but not essential; equivalent experience will also be considered.
- Previous experience in a quality, laboratory or regulated environment is desirable but not essential; full training will be provided.
- Strong administrative skills, with the ability to maintain accurate records and documentation.
- Proficiency with Microsoft Office applications (e.g. Word, Excel, Outlook, PowerPoint).
- High attention to detail, with a focus on accuracy and quality of work.
- Ability to prioritise and manage your own workload, working to deadlines while maintaining high standards.
- Strong communication skills and the ability to work effectively with colleagues at all levels.
What We Offer
- A standard benefits package, including core employee benefits in line with UK employment practices.
- The opportunity to develop your skills in quality management and regulatory standards, with exposure to ISO 9001, ISO 13485 and ISO 17025.
- Experience working with a structured QMS and involvement in a wide range of quality activities, from investigations to audits and product release.
- A professional working environment where your contribution to maintaining high quality standards is recognised and valued.
We welcome applications from all suitably qualified candidates, regardless of age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, or sexual orientation, in line with the Equality Act 2010. All offers of employment will be subject to the right to work in the UK and any other relevant pre-employment checks. Any personal data you provide during the recruitment process will be handled in accordance with applicable data protection laws, including the UK GDPR.
If you are ready to take the next step in your quality career and contribute to robust, compliant and efficient processes, we'd love to hear from you. Please submit your CV and any supporting information explaining how you meet the requirements of the role and join our team as we continue to strengthen our quality performance.
Come Be Part Of A Mission that Matters! From inside the farm gate to our dinner plates, Neogen protects the world’s food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there — and you can be too.
Quality Engineer employer: Neogen Corporation
Contact Detail:
Neogen Corporation Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Engineer
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its quality standards. Be ready to discuss how your skills align with their needs, especially around QMS activities and compliance. Show them you’re not just a fit, but the perfect fit!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online resources to refine your answers. Focus on articulating your attention to detail and structured approach, as these are key for a Quality Engineer role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining our mission to maintain high-quality standards.
We think you need these skills to ace Quality Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Quality Engineer role. Highlight any relevant experience in quality management systems or regulatory environments, even if it’s from a different field.
Showcase Your Attention to Detail: Since attention to detail is key for this role, use your application to demonstrate this trait. Double-check your documents for typos and ensure all information is accurate and well-organised.
Be Clear and Concise: When writing your supporting information, get straight to the point. Use clear language to explain how you meet the job requirements, and don’t be afraid to show your enthusiasm for the role!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role as quickly as possible!
How to prepare for a job interview at Neogen Corporation
✨Know Your QMS Inside Out
Make sure you understand the core Quality Management System (QMS) activities mentioned in the job description. Brush up on CAPAs, investigations, and change controls, as these are likely to come up during your interview. Being able to discuss these topics confidently will show that you're serious about the role.
✨Showcase Your Attention to Detail
Since this position requires a strong attention to detail, prepare examples from your past experiences where your meticulous nature made a difference. Whether it was catching an error in documentation or ensuring compliance with standards, having specific anecdotes ready will highlight your suitability for the role.
✨Prepare for Root Cause Analysis Questions
Expect questions around root cause analysis and continuous improvement. Think of situations where you identified a problem, conducted an analysis, and implemented a solution. This will demonstrate your analytical skills and your proactive approach to quality management.
✨Familiarise Yourself with ISO Standards
Since the role involves maintaining ISO certifications, it’s beneficial to have a basic understanding of ISO 9001, ISO 13485, and ISO 17025. You don’t need to be an expert, but being able to discuss how these standards apply to quality management will impress your interviewers and show your commitment to the field.