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- Tasks: Ensure compliance with ISO9001 and support quality management processes.
- Company: Join AnalytiChem, a leader in cleanroom microbiology solutions since 1971.
- Benefits: Full-time role with a dynamic work environment and growth opportunities.
- Why this job: Make a real impact on quality assurance in a fast-growing international organisation.
- Qualifications: Five years of QA experience and proficiency in Microsoft Office required.
- Other info: Be part of a collaborative team focused on continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
Based in Bicester since 1971, we are experts in cleanroom microbiology solutions, providing environmental monitoring and process validation support to healthcare, pharmaceutical, and industrial laboratories. Supported by ISO 9001 certification and a long-standing commitment to growth and quality, we manufacture the Redipor® range of microbiological media and offer specialized air monitoring and decontamination equipment, ensuring high-quality solutions tailored to customer requirements.
Today, AnalytiChem supports laboratories worldwide with a portfolio of specialized laboratory equipment, reagents, and consumables designed to help customers make better measurements in analytical chemistry and microbiology. We create high-quality culture media, reference materials, laboratory consumables, and sample preparation equipment that support the measurements that matter in everyday life.
If you are looking for a dynamic work environment within a fast-growing international organization, where quality, collaboration, and continuous improvement are at the heart of what we do, AnalytiChem may be the place for you.
The QA Specialist is part of a small team who are responsible for the continued compliance of our quality management system to ISO9001. This is a full time, onsite role (Monday to Friday, 08:00 – 16:00), reporting to the QA Manager.
Quality Assurance is responsible for the implementation and maintenance of the company quality management system which is currently registered to ISO9001:2015. The Quality Assurance Team are also responsible for all aspects related to quality management, non-conformance reporting, corrective and preventative action monitoring, internal and third party auditing, process validations, etc.
- Continued compliance of quality management system to ISO9001 and customer expectations
- Supporting all quality functions to ensure the needs of the business are met
- Supporting all business functions as and when required in a quality assurance capacity
- Other project goals as may be discussed and assigned
Actively support and maintain the Quality Management System to ensure ongoing compliance with ISO9001 standards. Support with overseeing the day-to-day processes of the QA team.
- Lead on non-conformances, technical changes and complaints process ensuring timely resolution and effectiveness of corrective actions
- Supporting the document control process for all documents across the business
- Support EQMs training initiatives
- Provide support to business areas on quality and compliance related issues
- Supporting and deputising for the QA Manager
- Ensure all clean room monitoring is recorded and reported as required
- Produced cleanroom critical control points which include environmental monitoring, temperature control, room pressures and water system reports for the Quality team and the wider business
- Update QA KPIs in a timely manner
- Adaptable – developing our products, packaging, and processes to meet our customer needs alongside supporting development for our colleagues
- Team player with a flexible, conscientious, and proactive approach
- Meticulous attention to detail, particularly in the review and analysis of data
- Ability to work independently with minimal supervision
Minimum of five years’ experience in a Quality Assurance role is essential. Experience of a QA role within manufacturing is desirable. Highly proficient in Microsoft Office applications (Word, Excel, PowerPoint, Outlook). Experience in the use and deployment of electronic Quality Management Systems (eQMS). Demonstrated experience in CAPA (Corrective and Preventive Actions) and complaint management. Experience working in a continuous improvement environment, using data to drive quality enhancements. Solid understanding and hands-on experience with ISO 9001 implementation and maintenance.
Join our Team as a QA Specialist and help shape quality excellence at AnalytiChem!
Please submit your updated English CV. For questions, contact our Talent Acquisition team using the details provided in the job post.
Quality Specialist - Training in Bicester employer: AnalytiChem Group
Contact Detail:
AnalytiChem Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Specialist - Training in Bicester
✨Tip Number 1
Network like a pro! Reach out to current employees at AnalytiChem on LinkedIn or other platforms. Ask them about their experiences and any tips they might have for landing the QA Specialist role. Personal connections can make a huge difference!
✨Tip Number 2
Prepare for the interview by brushing up on ISO 9001 standards and quality management systems. Be ready to discuss your past experiences with CAPA and how you've driven continuous improvement in previous roles. Show us you know your stuff!
✨Tip Number 3
Don’t just wait for the job to come to you! Apply through our website and make sure your application stands out. Tailor your CV to highlight your relevant experience in quality assurance and manufacturing. We want to see what makes you the perfect fit!
✨Tip Number 4
Follow up after your interview! A quick thank-you email can go a long way in showing your enthusiasm for the role. Mention something specific from the interview to remind us of your great conversation and keep you top of mind.
We think you need these skills to ace Quality Specialist - Training in Bicester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Quality Specialist role. Highlight your QA experience, especially in ISO 9001 compliance, to show us you’re the right fit!
Showcase Your Attention to Detail: In quality assurance, attention to detail is key! Use specific examples in your application to demonstrate how you've successfully managed data analysis or non-conformance reporting in the past.
Be Clear and Concise: When writing your application, keep it straightforward. We appreciate clarity, so avoid jargon and get straight to the point about your qualifications and why you want to join our team.
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 don’t miss any important updates from our Talent Acquisition team!
How to prepare for a job interview at AnalytiChem Group
✨Know Your ISO 9001 Inside Out
Make sure you brush up on your knowledge of ISO 9001 standards. Be prepared to discuss how you've implemented and maintained these standards in previous roles. This will show that you understand the core of what the company values in quality assurance.
✨Showcase Your Attention to Detail
Since this role requires meticulous attention to detail, come ready with examples from your past experiences where your keen eye made a difference. Whether it was catching a non-conformance or improving a process, specific stories will help illustrate your capabilities.
✨Be a Team Player
The job description highlights the importance of collaboration. Think of instances where you worked effectively within a team, especially in a QA context. Emphasising your ability to support colleagues and adapt to their needs will resonate well with the interviewers.
✨Prepare for Scenario-Based Questions
Expect questions that put you in hypothetical situations related to quality management. Practice responding to scenarios involving CAPA or complaint management. This will demonstrate your problem-solving skills and your proactive approach to quality assurance.
