7 Food Production jobs in Northern Ireland
Quality Control Specialist
Posted today
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Job Description
Requisition ID: 60790
Position Type: FT Fixed Term
Workplace Arrangement: #LI-Onsite
Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
About the roleThis is a fixed-term, onsite position based in Portadown, Northern Ireland, running until the end of August 2026, with the potential for extension.
The site specialises in the production of cheese blocks, sliced cheese, and grated cheese bags.
As a Quality Control Specialist, you will support the technical team by conducting routine inspections, monitoring production processes, and ensuring compliance with food safety standards. You'll assist with audits, equipment calibrations, data reporting, and documentation management. The role also involves cross-functional collaboration to uphold site standards and contribute to quality improvement initiatives.
Key responsibilitiesAs a Quality Control Specialist, you will:
- Play a key role in maintaining product integrity and food safety standards
- Conduct routine inspections and monitor production processes
- Support the technical team with problem-solving on the factory floor
- Assist with equipment calibrations and preparation for external audits
- Carry out internal audits including glass & perspex, pest control, and temperature checks
- Trend and report data, including results from the daily Taste Panel
- Manage samples, traceability documentation, and ensure technical records are audit-ready
- Collaborate with all departments to uphold site standards
- Contribute to ongoing quality improvement initiatives across the site
- Perform other day-to-day tasks as requested to support quality and technical operations
- Experience in a food manufacturing or quality control environment
- Solid understanding of food safety standards and regulatory compliance
- Familiarity with laboratory testing methods and equipment
- Competence in using Microsoft Office and quality management systems (e.g., SAP, QMS)
- 25 days annual leave (excluding bank holidays)
- Matched pension scheme
- Access to our employee development platform and Udemy learning resources
- Benefits platform offering discounts and cashback at major retailers
- A collaborative and inclusive work environment with opportunities for career growth
Kerry is an Equal Opportunities Employer. Consistent with our policy of providing equality of opportunity for all, we are required to seek particular information from applicants. As part of your application you will be asked to answer a short number of questions. This information will be held separate to your application and treated in the strictest of confidence.
Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
Recruiter: #LI-MU1
Posting Type: LI
Lead Quality Control Engineer
Posted 11 days ago
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Job Description
- Develop, implement, and maintain comprehensive quality control procedures and standards.
- Lead and manage the quality control team, including hiring, training, and performance evaluation.
- Design and execute quality assurance plans for new and existing products.
- Utilize statistical process control (SPC) techniques to monitor and improve manufacturing processes.
- Oversee root cause analysis for quality deviations and implement effective CAPA.
- Conduct internal audits and supplier quality assessments to ensure compliance.
- Interpret technical drawings, specifications, and quality standards.
- Collaborate with engineering and production teams to resolve quality issues.
- Manage quality documentation, records, and reporting.
- Drive continuous improvement initiatives to enhance product quality and efficiency.
- Ensure compliance with relevant industry regulations and certifications.
- Promote a strong quality-focused culture throughout the organization.
- Bachelor's degree in Engineering, Quality Management, or a related field.
- Minimum of 8 years of experience in quality control/assurance within a manufacturing environment.
- Proven experience in a leadership or supervisory role.
- In-depth knowledge of quality management systems (e.g., ISO 9001) and statistical tools (SPC, Six Sigma).
- Strong analytical and problem-solving skills with a data-driven approach.
- Excellent communication, interpersonal, and teamwork skills.
- Proficiency in quality management software and relevant IT tools.
- Ability to work independently and manage multiple priorities effectively in a remote setting.
- Experience with lean manufacturing principles is a plus.
- ASQ Certification (e.g., CQE, CQT) is highly desirable.
Senior Pharmaceutical Quality Control Manager
Posted 1 day ago
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Job Description
Key Responsibilities:
- Develop, implement, and manage the company's Quality Control (QC) strategy and systems.
- Oversee all QC laboratory operations, including testing of raw materials, in-process samples, and finished products.
- Ensure compliance with current Good Manufacturing Practices (GMP) and relevant regulatory guidelines (e.g., FDA, EMA, MHRA).
- Validate analytical methods and ensure equipment calibration and maintenance programs are in place.
- Manage stability testing programs and interpret study data.
- Review and approve QC documentation, including test records, specifications, and reports.
- Lead, mentor, and develop a team of QC analysts, fostering a culture of quality excellence.
- Conduct investigations into Out-of-Specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
- Liaise with regulatory agencies during inspections and audits.
- Stay current with advancements in pharmaceutical quality control and regulatory requirements.
Qualifications and Experience:
- Advanced degree (M.Sc. or Ph.D.) in Pharmacy, Chemistry, or a related scientific discipline.
- Extensive experience in pharmaceutical Quality Control, with a significant portion in a management or leadership role.
- In-depth knowledge of GMP, ICH guidelines, and pharmaceutical quality systems.
- Strong expertise in analytical techniques commonly used in pharmaceutical QC (e.g., HPLC, GC, spectroscopy).
- Proven experience in method validation, stability studies, and OOS investigations.
- Excellent leadership, team management, and communication skills.
- Strong analytical and problem-solving abilities.
- Ability to work independently, manage multiple projects, and thrive in a remote environment.
- Experience with regulatory submissions and audits is essential.
This is an exceptional opportunity for a seasoned Quality Control professional to take on a leadership role in a dynamic pharmaceutical company, working remotely. If you are passionate about ensuring product quality and compliance, we encourage you to apply.
Senior Quality Control Inspector - Automotive
Posted 14 days ago
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Senior Pharmaceutical Quality Control Analyst
Posted 21 days ago
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This is a remote role servicing operations related to Belfast, Northern Ireland, UK.
Senior Pharmaceutical Quality Control Analyst
Posted 24 days ago
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Job Description
Key Responsibilities:
- Perform quantitative and qualitative analysis of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, KF).
- Develop, validate, and transfer analytical methods in accordance with regulatory requirements.
- Calibrate and maintain laboratory equipment, ensuring its optimal performance.
- Review and interpret analytical data, ensuring accuracy and compliance with specifications.
- Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
- Prepare and review batch release documentation and certificates of analysis.
- Contribute to the continuous improvement of QC processes and procedures.
- Ensure adherence to Good Manufacturing Practices (GMP) and other relevant regulatory standards.
- Train and mentor junior QC analysts.
- Participate in internal and external audits as required.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Science, or a related field.
- Minimum of 5 years of experience in pharmaceutical Quality Control, with a strong focus on analytical testing.
- Proven expertise in operating and troubleshooting various analytical instruments (HPLC, GC, etc.).
- In-depth knowledge of GMP regulations and quality control principles.
- Experience with method validation and OOS investigations.
- Excellent documentation, data integrity, and organisational skills.
- Strong analytical and problem-solving abilities.
- Proficiency in laboratory information management systems (LIMS) is desirable.
- Ability to work effectively in a team and independently.
This role offers a significant opportunity to contribute to the highest standards of pharmaceutical quality and safety within a reputable organisation.
Senior Quality Control Engineer - Automotive Manufacturing
Posted 14 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, implement, and manage comprehensive quality control plans and procedures throughout the manufacturing lifecycle.
- Conduct regular inspections and audits of production lines, components, and finished products to ensure adherence to specifications and standards.
- Analyze quality data, identify root causes of defects, and implement corrective and preventive actions (CAPA).
- Lead and mentor a team of quality assurance technicians and inspectors, providing training and guidance.
- Collaborate closely with engineering, production, and supply chain teams to resolve quality issues promptly.
- Ensure compliance with relevant automotive industry standards such as IATF 16949 and ISO 9001.
- Develop and maintain quality documentation, including inspection reports, non-conformance reports (NCRs), and process control documents.
- Drive continuous improvement initiatives using methodologies like Six Sigma and Lean Manufacturing to enhance product quality and reduce waste.
- Manage customer feedback and warranty claims related to product quality, implementing necessary improvements.
- Oversee the calibration and maintenance of testing and measurement equipment.
- Bachelor's degree in Engineering (Mechanical, Electrical, Manufacturing, or related field).
- Minimum of 5 years of experience in quality control or quality assurance within the automotive manufacturing sector.
- In-depth knowledge of quality management systems (QMS), particularly IATF 16949 and ISO 9001.
- Proven experience with statistical process control (SPC), root cause analysis (RCA), and CAPA methodologies.
- Strong understanding of manufacturing processes, particularly in automotive assembly and component production.
- Excellent analytical, problem-solving, and decision-making skills.
- Proficiency in quality control tools and software.
- Strong leadership, communication, and team management abilities.
- Ability to interpret technical drawings and specifications.
- Experience with auditing processes and supplier quality management is a significant advantage.
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