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Job description
Lab Senior Technician Operative – Production Quality Assurance and Micro, East Kilbride
Interested in learning more about this job Scroll down and find out what skills, experience and educational qualifications are needed.Shift based (days and nights) – 42hr Annualised Hours (over 7 days)
Annual performance related pay bonus + Share scheme + Competitive pension contributions + Personal private medical insuance + Laundered uniform + All safety equipment provided + Subsidised canteen on-site + Free hot and cold drinks + Free parking + Excellent parental benefits
What you become part of:
East Kilbride Operations is a high performing manufacturing site producing around 20 million cases of drinks each year across six production lines, including both glass and PET formats. It is the only site in Great Britain producing Appletiser in glass, making it a unique and strategically important operation.
With approximately 200 colleagues on site, the environment is collaborative, fast paced, and supportive. Joining this team offers not only exposure to a complex and quality driven manufacturing environment, but also access to broader career opportunities across other GB sites and pan European locations.
What to expect:
In this role, you will be a key member of the QESH team, acting as a quality guardian on shift and ensuring products consistently meet the highest standards. You will combine hands on laboratory expertise with strong collaboration across production teams to drive compliance, quality, and continuous improvement.Key responsibilities include:Acting as the primary point of contact for quality on shift, providing expert guidance and escalation where requiredConducting analytical, sensory and microbiological testing in a consistent, controlled, and compliant mannerPerforming detailed analysis and supporting investigations to protect product integrity and QESH standardsMonitoring product compliance and supporting operational teams through hands on coaching, troubleshooting, and trainingManaging quality data and completing administrative tasks within the quality monitoring systems
You will also play an important role in ensuring equipment and processes are robust and reliable:Delivering the calibration programme to ensure all measuring equipment provides accurate and dependable resultsSupporting the implementation of the site Quality Plan and driving adherence to agreed ways of workingMaintaining high standards of safety, hygiene, and housekeeping, demonstrating a zero accident mindset
This role offers strong involvement in continuous improvement and capability building:Supporting the QA Lead and wider teams to achieve quality objectives and close audit actionsLeading or contributing to root cause investigations for non conformance and microbiological issuesDriving GMP standards through audits, engagement with colleagues, and continuous improvement initiativesWriting and developing laboratory procedures and ensuring effective training and verification within the team
In addition, you will contribute to the sensory and microbiological excellence of the site:Conducting enhanced sensory testing to support product release and maintain high quality standardsParticipating in proficiency testing and additional testing programmesManaging non conformance processes on shift, including initial investigation and sharing learnings across teams
Skills & Essentials:
To be successful in this role, you will bring a blend of technical expertise, attention to detail, and a proactive approach to quality and teamwork.Experience working within an FMCG or manufacturing environmentPractical understanding of Quality Assurance principles, with strong organisational and prioritisation skillsGood working knowledge of systems, including Microsoft OfficeMicrobiology knowledge or proven experience in a related field is advantageousHACCP qualification (Level 3 or above) is beneficialExperience of analytical testing and working to ISO standardsProven hands-on experience with HPLC operation . Interpret chromatographic data, troubleshoot instrumentation, and ensure accurate documentation of results.Strong understanding of chromatographic principles, sample preparation, and data analysis software.Ability to work to GLP/GMP standards with meticulous attention to detail.
Eligibility to work in the UK is required.
This is an excellent opportunity for someone looking to develop their career in a quality focused, high performing manufacturing environment, where their contribution has a direct impact on product excellence and customer satisfaction.
The closing date for applications is 01/06/26. We reserve the right to close this advertisement early if we receive a high volume of applications. To ensure you are considered for this role, we encourage you to apply as soon as possible.
We are Coca-Cola Europacific Partners (CCEP) – a dedicated team of 42,000 people, serving customers in 31 countries, who work together to make, move and sell some of the world’s most loved drinks.
We are a global business and one of the leading consumer goods companies in the world. We help our 2.1 million customers grow, and we are constantly investing in exciting new products, innovative technologies and fresh ideas. This helps us to delight the 600 million people who enjoy our drinks every day.
From gender, age and ethnicity to sexual orientation and different abilities, we welcome people from all walks of life and empower unique perspectives. We recognise we’ve got some way to go, but we’ll get there with the support of our people. It’s them who drive our future growth. To find out more about what it’s like to work at and our culture we would welcome you to speak to one of our employees on our live chat platform, just click here to .
We recognise some people prefer not to participate in alcohol related sales, interactions, or promotions. xcunqrw If that’s true for you – please raise this with your talent acquisition contact who will advise you on whether this role includes activities related to our alcohol portfolio.
