43 Lead Evaluator jobs in Ireland
Pharmacovigilance Data Analysis Manager
Dublin, Leinster
Grifols Shared Services North America, Inc
Posted 2 days ago
Job Viewed
Job Description
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
**We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us be outstanding.**
Help us lead one of the world's largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That's why we need a _Pharmacovigilance Data Analysis Manager_ like you.
Role Mission: Provide operational support for global pharmacovigilance activities related to Grifols' investigational and marketed products. Ensure high-quality pharmacovigilance deliverables that comply with global regulatory reporting timelines. Manage project implementation and execution of safety systems, including ongoing business support and continuous improvement initiatives. Act as a key liaison with IT system administrators to validate and test system changes, ensuring compliance and alignment with business needs.
**What your responsibilities will be**
+ Lead and coordinate safety data analysis for aggregate reports preparation, signal management and ad hoc requests.
+ Support drug safety systems through business administration tasks, including database configuration updates, submission rules management and testing with regulatory authorities.
+ Serve as a subject matter expert in delivering and evaluating cost-effective, sustainable solutions that meet business requirements.
+ Manage documentation related to PV systems and applications, including SOPs, WPs, user requirements, functional/ technical specifications and process flow diagrams.
+ Drive change management initiatives to ensure smooth adoption of new processes and support the integration of new applications within the PV team.
+ Collect, prioritize and plan system improvements based on user feedback, while ensuring compliance with regulatory requirements.
+ Act as the primary PV contact for IT-related PV projects.
+ Drive Innovation through AI in Pharmacovigilance: Stay at the forefront of artificial intelligence advancements to identify and evaluate innovative technologies and processes that can enhance pharmacovigilance operations. This includes proactively assessing AI-driven tools and methodologies to improve signal detection, case processing, data analysis and regulatory compliance. Collaborate cross-functionally to pilot and implement solutions that increase efficiency, accuracy, and strategic value in safety monitoring.
**Who you are**
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
+ You have a bachelor's degree in Health Sciences (pharmacy, nursing, medicine, veterinary, etc) or Bioscience (biochemistry, biotechnology, biology, etc). Additional training and/or experience in bioinformatics/biostatistics or data analysis tools (such as R or Power BI).
+ You have at least 4 years of pharmacovigilance experience including management of pharmacovigilance data bases.
+ You have proven knowledge of Good Pharmacovigilance Practices; existing legislation, regulations, guidelines, medical coding and safety-data administration.
+ You are proficient in Windows and MS Office (Excel, PowerPoint, Visio, Word).
+ Familiarity with reporting tools such as Business Objects is strongly preferred.
+ You have knowledge of E2b (R2) and E2b (R3) and to be familiarity with medical terminology, MedDRA, WhoDrug are a plus.
+ You speak fluent Spanish and English.
+ You are proven self-starter with strong work ethic and the ability to exercise good judgment.
+ You must be proactive, results oriented and have strong attention to detail.
+ Strong organizational, analytical and problem-solving skills with the ability to make structured decisions on a routine basis.
+ Strong interpersonal skills with the ability to interact and collaborate with personnel at all levels in a team environment.
+ You possess strong technical writing and communication skills with ability to create and present design proposals, test scripts, execute training sessions and conduct effective meetings.
+ Ability to effectively prioritize and manage multiple tasks to ensure successful completion targeted deadlines.
**What we offer**
It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.
Information about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to apply!
We look forward to receiving your application!
**We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.**
Grifols is an equal opportunity employer.
**Flexible schedule:** Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).
**Benefits package**
**Contract of Employment:** Permanent position
**Flexibility for U Program:** Hybrid
**Location:** Sant Cugat del Vallès (preferably) / Other locations as Los Angeles, Clayton or Dublin will be considered
more about Grifols
**Req ID:**
**Type:** Indefinido tiempo completo
**Job Category:** I + D
**We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us be outstanding.**
Help us lead one of the world's largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That's why we need a _Pharmacovigilance Data Analysis Manager_ like you.
Role Mission: Provide operational support for global pharmacovigilance activities related to Grifols' investigational and marketed products. Ensure high-quality pharmacovigilance deliverables that comply with global regulatory reporting timelines. Manage project implementation and execution of safety systems, including ongoing business support and continuous improvement initiatives. Act as a key liaison with IT system administrators to validate and test system changes, ensuring compliance and alignment with business needs.
**What your responsibilities will be**
+ Lead and coordinate safety data analysis for aggregate reports preparation, signal management and ad hoc requests.
+ Support drug safety systems through business administration tasks, including database configuration updates, submission rules management and testing with regulatory authorities.
+ Serve as a subject matter expert in delivering and evaluating cost-effective, sustainable solutions that meet business requirements.
+ Manage documentation related to PV systems and applications, including SOPs, WPs, user requirements, functional/ technical specifications and process flow diagrams.
+ Drive change management initiatives to ensure smooth adoption of new processes and support the integration of new applications within the PV team.
+ Collect, prioritize and plan system improvements based on user feedback, while ensuring compliance with regulatory requirements.
+ Act as the primary PV contact for IT-related PV projects.
+ Drive Innovation through AI in Pharmacovigilance: Stay at the forefront of artificial intelligence advancements to identify and evaluate innovative technologies and processes that can enhance pharmacovigilance operations. This includes proactively assessing AI-driven tools and methodologies to improve signal detection, case processing, data analysis and regulatory compliance. Collaborate cross-functionally to pilot and implement solutions that increase efficiency, accuracy, and strategic value in safety monitoring.
**Who you are**
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
+ You have a bachelor's degree in Health Sciences (pharmacy, nursing, medicine, veterinary, etc) or Bioscience (biochemistry, biotechnology, biology, etc). Additional training and/or experience in bioinformatics/biostatistics or data analysis tools (such as R or Power BI).
+ You have at least 4 years of pharmacovigilance experience including management of pharmacovigilance data bases.
+ You have proven knowledge of Good Pharmacovigilance Practices; existing legislation, regulations, guidelines, medical coding and safety-data administration.
+ You are proficient in Windows and MS Office (Excel, PowerPoint, Visio, Word).
+ Familiarity with reporting tools such as Business Objects is strongly preferred.
+ You have knowledge of E2b (R2) and E2b (R3) and to be familiarity with medical terminology, MedDRA, WhoDrug are a plus.
+ You speak fluent Spanish and English.
+ You are proven self-starter with strong work ethic and the ability to exercise good judgment.
+ You must be proactive, results oriented and have strong attention to detail.
+ Strong organizational, analytical and problem-solving skills with the ability to make structured decisions on a routine basis.
+ Strong interpersonal skills with the ability to interact and collaborate with personnel at all levels in a team environment.
+ You possess strong technical writing and communication skills with ability to create and present design proposals, test scripts, execute training sessions and conduct effective meetings.
+ Ability to effectively prioritize and manage multiple tasks to ensure successful completion targeted deadlines.
**What we offer**
It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.
Information about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to apply!
We look forward to receiving your application!
**We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.**
Grifols is an equal opportunity employer.
**Flexible schedule:** Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).
**Benefits package**
**Contract of Employment:** Permanent position
**Flexibility for U Program:** Hybrid
**Location:** Sant Cugat del Vallès (preferably) / Other locations as Los Angeles, Clayton or Dublin will be considered
more about Grifols
**Req ID:**
**Type:** Indefinido tiempo completo
**Job Category:** I + D
This advertiser has chosen not to accept applicants from your region.
0
Quality Assurance Engineer
Acuity Brands
Posted 2 days ago
Job Viewed
Job Description
Acuity Inc. (NYSE: AYI) is a market-leading industrial technology company. We use technology to solve problems in spaces, light and more things to come. Through our two business segments, Acuity Brands Lighting (ABL) and Acuity Intelligent Spaces (AIS), we design, manufacture, and bring to market products and services that make a valuable difference in people's lives.
We achieve growth through the development of innovative new products and services, including lighting, lighting controls, building management solutions, and an audio, video and control platform. We focus on customer outcomes and drive growth and productivity to increase market share and deliver superior returns. We look to aggressively deploy capital to grow the business and to enter attractive new verticals.
Our Digital Centre of Excellence in Cork, Ireland brings together the best of Acuity's technologies, serving as a hub for research and development to build software expertise, innovation and capacity. Our Digital Centre of Excellence in Cork is more than a workplace - it's a hub for innovation, collaboration, and growth. We're building a team of disruptive thinkers, data-forward engineers, and product innovators who are shaping the future of our technology.
We offer:
+ Meaningful Work: Solve real-world problems, guided by our Better.Smarter.Faster. operating system, through cutting-edge software, AI, and data solutions.
+ Growth & Development: Access to global learning experiences, mentorship, and career mobility.
+ Health & Well-Being: Comprehensive benefits and wellness programs tailored to support you.
+ Values Driven Culture: Become part of an environment where the best people come to do their best work.
+ Global Reach, Local Impact: Be part of a multinational company while contributing to Cork's vibrant tech ecosystem.
Acuity Inc. is based in Atlanta, Georgia, with operations across North America, Europe and Asia. The Company is powered by approximately 13,000 dedicated and talented associates. Visit us at . Explore opportunities in Ireland at acuityinc.ie/careers .
**Location** : Cork, Ireland (On-site)
**Job Summary**
We are seeking detail-oriented and strong Technical QA Engineers to join our team in Ireland. In this role, you will have the responsibility of ensuring the quality and reliability of software and systems through rigorous testing, automation, and process improvement. You will design, develop and execute test cases as well as collaborate across a highly matrixed team of developers, product managers and stakeholders. You will support release management and post-deployment validation, conduct functional, regression, integration and performance testing.
Successful candidates must have a strong understanding of QA methodologies, software development life cycles, and regulatory compliance standards relevant to the Irish and EU markets.
**Minimum Qualifications**
+ Bachelor's degree in Computer Science, Engineering, or related field.
+ Relevant experience in test automation tools and programming/scripting languages.
+ Preferred experience in using Co-Pilot or other AI applications.
We value diversity and are an equal opportunity employer. All qualified applicants will be considered for employment without regards to race, color, age, gender, sexual orientation, gender identity and expression, ethnicity or national origin, disability, pregnancy, religion, covered veteran status, protected genetic information, or any other characteristic protected by law. Please click here ( and here ( for more information.
Accommodation for Applicants with Disabilities: As an equal opportunity employer, Acuity Inc. is committed to providing reasonable accommodations in its application process for qualified individuals with disabilities and disabled veterans. If you have difficulty using our online system due to a disability and need an accommodation, you may contact us at . Please clearly indicate what type of accommodation you are requesting and for what requisition.
Any unsolicited resumes sent to Acuity Inc. from a third party, such as an Agency recruiter, including unsolicited resumes sent to an Acuity Inc. mailing address, fax machine or email address, directly to Acuity Inc. employees, or to Acuity Inc. resume database will be considered Acuity Inc. property. Acuity Inc. will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Acuity Inc. will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor, but does not have the appropriate approvals to be engaged on a search.
E-Verify Participation Poster ( (
We achieve growth through the development of innovative new products and services, including lighting, lighting controls, building management solutions, and an audio, video and control platform. We focus on customer outcomes and drive growth and productivity to increase market share and deliver superior returns. We look to aggressively deploy capital to grow the business and to enter attractive new verticals.
Our Digital Centre of Excellence in Cork, Ireland brings together the best of Acuity's technologies, serving as a hub for research and development to build software expertise, innovation and capacity. Our Digital Centre of Excellence in Cork is more than a workplace - it's a hub for innovation, collaboration, and growth. We're building a team of disruptive thinkers, data-forward engineers, and product innovators who are shaping the future of our technology.
We offer:
+ Meaningful Work: Solve real-world problems, guided by our Better.Smarter.Faster. operating system, through cutting-edge software, AI, and data solutions.
+ Growth & Development: Access to global learning experiences, mentorship, and career mobility.
+ Health & Well-Being: Comprehensive benefits and wellness programs tailored to support you.
+ Values Driven Culture: Become part of an environment where the best people come to do their best work.
+ Global Reach, Local Impact: Be part of a multinational company while contributing to Cork's vibrant tech ecosystem.
Acuity Inc. is based in Atlanta, Georgia, with operations across North America, Europe and Asia. The Company is powered by approximately 13,000 dedicated and talented associates. Visit us at . Explore opportunities in Ireland at acuityinc.ie/careers .
**Location** : Cork, Ireland (On-site)
**Job Summary**
We are seeking detail-oriented and strong Technical QA Engineers to join our team in Ireland. In this role, you will have the responsibility of ensuring the quality and reliability of software and systems through rigorous testing, automation, and process improvement. You will design, develop and execute test cases as well as collaborate across a highly matrixed team of developers, product managers and stakeholders. You will support release management and post-deployment validation, conduct functional, regression, integration and performance testing.
Successful candidates must have a strong understanding of QA methodologies, software development life cycles, and regulatory compliance standards relevant to the Irish and EU markets.
**Minimum Qualifications**
+ Bachelor's degree in Computer Science, Engineering, or related field.
+ Relevant experience in test automation tools and programming/scripting languages.
+ Preferred experience in using Co-Pilot or other AI applications.
We value diversity and are an equal opportunity employer. All qualified applicants will be considered for employment without regards to race, color, age, gender, sexual orientation, gender identity and expression, ethnicity or national origin, disability, pregnancy, religion, covered veteran status, protected genetic information, or any other characteristic protected by law. Please click here ( and here ( for more information.
Accommodation for Applicants with Disabilities: As an equal opportunity employer, Acuity Inc. is committed to providing reasonable accommodations in its application process for qualified individuals with disabilities and disabled veterans. If you have difficulty using our online system due to a disability and need an accommodation, you may contact us at . Please clearly indicate what type of accommodation you are requesting and for what requisition.
Any unsolicited resumes sent to Acuity Inc. from a third party, such as an Agency recruiter, including unsolicited resumes sent to an Acuity Inc. mailing address, fax machine or email address, directly to Acuity Inc. employees, or to Acuity Inc. resume database will be considered Acuity Inc. property. Acuity Inc. will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Acuity Inc. will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor, but does not have the appropriate approvals to be engaged on a search.
E-Verify Participation Poster ( (
This advertiser has chosen not to accept applicants from your region.
1
Quality Assurance Manager
Dundalk, Leinster
Hunter Savage
Posted 10 days ago
Job Viewed
Job Description
Job Title: Quality Assurance Manager Location: Drogheda, Ireland Salary: €45,000 DOE Overview: An excellent opportunity has arisen for an experienced Quality Assurance Manager to join a leading FMCG food manufacturer with a portfolio of well-known household brands. This is a fantastic chance to become part of a business with ambitious growth plans, where you will play a key role in maintaining the highest standards of food safety and quality. Key Responsibilities: Lead and continuously improve the FSSC22000 certified quality management system. Act as the site champion for quality, ensuring standards are consistently met and exceeded. Manage and oversee internal auditing to ISO/FSSC standards. Lead the HACCP team and take ownership of allergen management. Manage incoming inspections and carry out daily quality control checks. Oversee hygiene and food safety auditing across the site. Partner with New Product Development to ensure quality standards in innovation projects. Deliver staff training on QA procedures and hygiene practices. Maintain sampling plans and coordinate laboratory analysis of raw materials. Manage raw material supplier approval, specifications, and documentation for both raw materials and finished goods. Liaise with Customer Services on complaint investigations, ensuring timely resolutions. Act as the technical point of contact for regulatory bodies and customers. Contribute as a member of the site Health & Safety Team. Present updates and insights at weekly stand-up meetings. The Person: 4-5 years' experience in a Quality role within FMCG food manufacturing. Strong knowledge of Food Safety and Quality Management Systems (FSSC22000 & BRC). Proven ability to work independently as well as collaboratively in a team. A continuous improvement mindset with strong attention to detail. Demonstrated leadership skills with the ability to influence and engage teams. Excellent communication and IT skills. Skills: QA Quality Assurance
This advertiser has chosen not to accept applicants from your region.
2
Quality Assurance Specialist
Cork, Munster
Catalyx
Posted 13 days ago
Job Viewed
Job Description
Catalyx is seeking a Quality Assurance Specialist to join our team and work on our customer site in Cork. This role operates on a rotating weekly shift pattern, alternating between morning and evening shifts. Who We Are: Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes-globally-with a sophisticated blend of products, technologies, and lifecycle services. The company was formed in 2022 after CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies joined forces. For over three decades, Catalyx's partnership-based culture has helped organizations in production-intense, highly regulated industries optimize their operational efficiency, performance, and safety. To learn more about the company's experience and comprehensive suite of capabilities and solutions, visit . The Role: Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations. Responsibilities: Provide quality oversight across various production stages, including material inspection, in-process control, and product readiness activities. Assemble and review documentation to support product disposition, working closely with operational and quality colleagues to meet release timelines. Support packaging operations by conducting visual inspections and ensuring process adherence during routine activities. Collaborate with cross-functional teams (Manufacturing, Quality Control, Supply Chain, Engineering, etc.) to resolve day-to-day queries and issues efficiently. Contribute to the maintenance and improvement of quality systems through change control, deviation management, and CAPA oversight. Conduct documentation reviews such as batch records, SOPs, and WI updates, ensuring alignment with regulatory and internal standards. Participate in the preparation of periodic quality reports and metrics, supporting trend identification and ongoing improvement. Engage in internal audits and readiness assessments to ensure site and process compliance. Provide knowledge-sharing and informal coaching on quality processes to enable operational teams to work effectively within GMP frameworks. Support project-based work and initiatives aimed at process enhancement and improved compliance practices. Review and approve manufacturing inputs and documents to ensure compliance with release criteria. Requirements: Bachelor's degree in a scientific or technical discipline. Minimum 3 years' experience in a Quality or GMP-related role within the pharmaceutical, biotech or related regulated sector. Familiarity with batch documentation, quality systems, and regulatory expectations (e.g., FDA, EMA). Ability to analyse issues, identify appropriate corrective actions, and escalate where necessary. Experience supporting or interacting with packaging or material management processes is beneficial. Strong written and verbal communication skills; confident working in a collaborative environment. Competence with Microsoft Office tools, particularly Excel and Word. Organised, detail-focused, and capable of managing multiple priorities. Comfortable working independently within defined parameters, and adaptable to shifting project needs Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
This advertiser has chosen not to accept applicants from your region.
3
Quality Assurance Analyst
Cork, Munster
Clearstream Fund Centre S.A., Cork Branch
Posted 13 days ago
Job Viewed
Job Description
Build the future of financial markets. Build yours. Ready to make a real impact in the financial industry? At Deutsche Brse Group, we'll empower you to grow your career in a supportive and inclusive environment. With our unique business model, driven by 15,000 colleagues around the globe, we actively shape the future of financial markets. Join our One Global Team! Who we are Deutsche Brse Group is one of the world's leading exchange organisations and an innovative market infrastructure provider. With our products and services, we ensure that capital markets are fair, transparent, reliable, and stable. Together, we develop state-of-the-art IT solutions and offer our IT systems all over the world. Within the Deutsche Brse Group, Clearstream is an international central securities depository (ICSD). It provides post-trade infrastructure and securities services for the international market and 59 domestic markets worldwide, with customers in 110 countries. Cork Your career at Deutsche Brse Group Your area of work The Quality Control Officer is responsible for ensuring the accuracy, consistency, and completeness of regulatory reporting outputs across KIIDs, PRIIPs and ESG domains. This role supports the delivery of high-quality reports by performing detailed quality checks, identifying discrepancies, and driving continuous improvement in data validation and reporting processes. Your responsibilities Perform detailed quality control checks on KIIDs, PRIIPs and ESG reports prior to client delivery, ensuring alignment with regulatory standards and internal quality benchmarks. Identify and document errors, inconsistencies, and missing narratives across reporting outputs. Collaborate with Regulatory Reporting Agents to validate data sources and ensure accurate interpretation of regulatory requirements. Monitor and report on recurring quality issues, contributing to root cause analysis and recommending corrective actions. Support the enhancement of validation tools and processes to reduce false positives and improve reporting accuracy. Maintain quality logs and KPIs to track performance and support post-production reviews. Liaise with internal teams to ensure timely resolution of quality issues and escalate critical findings to management. Assist in the development and implementation of quality assurance procedures and best practices. Participate in assigned training and stay updated on regulatory changes impacting reporting standards. Act and work in compliance with all internal rules and policies. Your profile A minimum of 3 years of post-graduate education, preferably in Finance, Data Management, or a related field At least 2 years of experience in a quality assurance, data validation, or regulatory reporting role Understanding of ESG, KIID, and PRIIPs reporting standards and regulatory frameworks Proficiency in English; additional languages are an asset Advanced Microsoft Excel skills and familiarity with data validation tools Excellent attention to detail and analytical skills Strong communication and interpersonal skills Proactive, solution-oriented mindset with a collaborative approach Ability to work independently and manage multiple priorities
This advertiser has chosen not to accept applicants from your region.
4
Quality Assurance Technician
Monaghan, Ulster
Vickerstock UK
Posted 10 days ago
Job Viewed
Job Description
Quality Assurance Technician Co Monaghan Fulltime/Permanent Monday - Friday, 40 Hours Attractive Salary Vickerstock are working in partnership with our specialist food processing client in Ireland and UK who have doubled production in the last 5 years and continues to do so, due to this they are seeking a full time/permanent Quality Assurance Technician to join the team at their site in County Monaghan. As a Quality Assurance Technician reporting to the Quality & Technical Manager, you will be responsible for: Lead the development, implementation, and monitoring of the Food Safety Management System (FSMS), including HACCP, prerequisite programmes, and SOPs. Ensure compliance with legislation, BRC, and customer standards, report performance and compliance status to the Technical Manager. Conduct and report internal audits, driving effective close-outs with management and supervisors. Investigate customer complaints and external non-conformances, ensuring robust root cause analysis and timely corrective/preventive actions. Analyse Production Quality KPIs, identify trends, and collaborate with production teams to resolve issues and drive improvement. Apply Lean principles in daily problem-solving, root cause analysis, and change management initiatives. Proactively identify hazards, manage risks, and implement continuous improvement measures to safeguard product safety. Lead and deliver cross-functional projects, ensuring timely completion and stakeholder engagement. Work closely with Production and Maintenance teams to set standards, solve problems, and implement sustainable solutions. We are looking for: Minimum recognised 3rd level qualification in a Food Science related discipline. Minimum 3 years+ Quality Assurance/Quality Control experience in Food Manufacturing environment Experience working with Quality Systems Have a demonstratable comprehensive knowledge of auditing, quality standards and systems, quality management techniques such as HACCP, Process Control, knowledge of food legislation, GFSI standards including BRC. Sound like the career move you've been after and would like to hear more, pick up the phone to Sophie now on or send an updated CV - in Word format - via the link on the page (or email). If this opportunity doesn't quite get the taste buds flowing but like me you are passionate about food, let's get a chat and see how I can help grow your career. PLEASE VISIT OUR WEBSITE FOR A FULL LIST OF OUR CURRENT VACANCIES. Skills: Quality Assurance Technician Quality Technician Quality Assurance Quality Control Senior Quality
This advertiser has chosen not to accept applicants from your region.
5
Quality Assurance Technician
Monaghan, Ulster
Hunter Savage
Posted 16 days ago
Job Viewed
Job Description
Job Title: Quality Assurance Technician Reporting to: Quality & Technical Manager Contract Type: Full-time, Permanent Location: Co. Monaghan Salary: €45,000 - €50,000 (DOE) Overview We are seeking an experienced Quality Assurance Technician to join a leading food manufacturing business based in Co. Monaghan. This role offers the opportunity to play a key part in driving quality and compliance across the site, ensuring the highest standards in food safety and technical performance. Key Responsibilities Support the effective development, implementation, and monitoring of the Food Safety Management System, including HACCP, prerequisite programmes, and SOPs. Report on site performance against standards, ensuring compliance with legislation, BRC, and customer requirements. Conduct internal audits, communicate findings, and collaborate with management to ensure timely and effective close-outs. Lead and manage projects to completion, engaging key stakeholders throughout. Apply Lean manufacturing principles to problem-solving, root cause analysis, and change management. Proactively identify and mitigate product safety risks, implementing corrective and preventative actions to drive continuous improvement. Analyse production quality KPIs, report trends, and collaborate with production teams to resolve issues. Investigate customer complaints and non-conformances, ensuring robust root cause analysis and timely corrective actions. Work closely with Production and Maintenance teams to set standards, address issues, and implement improvements. Requirements Degree or equivalent qualification in Food Science or related discipline. Minimum of 3+ years' QA/QC experience within a food manufacturing environment. Strong knowledge of auditing, HACCP, food legislation, BRC, and quality systems. Proven experience in continuous improvement and delivering sustainable change. Strong analytical and problem-solving skills, with a proactive and hands-on approach. Highly motivated team player with excellent communication and interpersonal skills. Proficiency in Excel and other IT systems. Strong organisational and time management skills, with the ability to thrive in a fast-paced environment. Skills: QA Technician
This advertiser has chosen not to accept applicants from your region.
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6
Quality assurance technician
Monaghan, Ulster
Vickerstock UK
Posted today
Job Viewed
Job Description
Quality Assurance Technician Co Monaghan Fulltime/Permanent Monday - Friday, 40 Hours Attractive Salary Vickerstock are working in partnership with our specialist food processing client in Ireland and UK who have doubled production in the last 5 years and continues to do so, due to this they are seeking a full time/permanent Quality Assurance Technician to join the team at their site in County Monaghan. As a Quality Assurance Technician reporting to the Quality & Technical Manager, you will be responsible for: Lead the development, implementation, and monitoring of the Food Safety Management System (FSMS), including HACCP, prerequisite programmes, and SOPs. Ensure compliance with legislation, BRC, and customer standards, report performance and compliance status to the Technical Manager. Conduct and report internal audits, driving effective close-outs with management and supervisors. Investigate customer complaints and external non-conformances, ensuring robust root cause analysis and timely corrective/preventive actions. Analyse Production Quality KPIs, identify trends, and collaborate with production teams to resolve issues and drive improvement. Apply Lean principles in daily problem-solving, root cause analysis, and change management initiatives. Proactively identify hazards, manage risks, and implement continuous improvement measures to safeguard product safety. Lead and deliver cross-functional projects, ensuring timely completion and stakeholder engagement. Work closely with Production and Maintenance teams to set standards, solve problems, and implement sustainable solutions. We are looking for: Minimum recognised 3rd level qualification in a Food Science related discipline. Minimum 3 years+ Quality Assurance/Quality Control experience in Food Manufacturing environment Experience working with Quality Systems Have a demonstratable comprehensive knowledge of auditing, quality standards and systems, quality management techniques such as HACCP, Process Control, knowledge of food legislation, GFSI standards including BRC. Sound like the career move you've been after and would like to hear more, pick up the phone to Sophie now on or send an updated CV - in Word format - via the link on the page (or email). If this opportunity doesn't quite get the taste buds flowing but like me you are passionate about food, let's get a chat and see how I can help grow your career. PLEASE VISIT OUR WEBSITE FOR A FULL LIST OF OUR CURRENT VACANCIES. Skills: Quality Assurance Technician Quality Technician Quality Assurance Quality Control Senior Quality
This advertiser has chosen not to accept applicants from your region.
7
Quality assurance technician
Monaghan, Ulster
Hunter Savage
Posted today
Job Viewed
Job Description
Job Title: Quality Assurance Technician Reporting to: Quality & Technical Manager Contract Type: Full-time, Permanent Location: Co. Monaghan Salary: €45,000 - €50,000 (DOE) Overview We are seeking an experienced Quality Assurance Technician to join a leading food manufacturing business based in Co. Monaghan. This role offers the opportunity to play a key part in driving quality and compliance across the site, ensuring the highest standards in food safety and technical performance. Key Responsibilities Support the effective development, implementation, and monitoring of the Food Safety Management System, including HACCP, prerequisite programmes, and SOPs. Report on site performance against standards, ensuring compliance with legislation, BRC, and customer requirements. Conduct internal audits, communicate findings, and collaborate with management to ensure timely and effective close-outs. Lead and manage projects to completion, engaging key stakeholders throughout. Apply Lean manufacturing principles to problem-solving, root cause analysis, and change management. Proactively identify and mitigate product safety risks, implementing corrective and preventative actions to drive continuous improvement. Analyse production quality KPIs, report trends, and collaborate with production teams to resolve issues. Investigate customer complaints and non-conformances, ensuring robust root cause analysis and timely corrective actions. Work closely with Production and Maintenance teams to set standards, address issues, and implement improvements. Requirements Degree or equivalent qualification in Food Science or related discipline. Minimum of 3+ years' QA/QC experience within a food manufacturing environment. Strong knowledge of auditing, HACCP, food legislation, BRC, and quality systems. Proven experience in continuous improvement and delivering sustainable change. Strong analytical and problem-solving skills, with a proactive and hands-on approach. Highly motivated team player with excellent communication and interpersonal skills. Proficiency in Excel and other IT systems. Strong organisational and time management skills, with the ability to thrive in a fast-paced environment. Skills: QA Technician
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Quality Assurance Technician, Intermediate
Clonmel, Munster
Abbott
Posted 1 day ago
Job Viewed
Job Description
Job Description
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Ireland Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**PURPOSE OF THE JOB**
Provides technical assistance to engineering to support
manufacturing efforts by implementing corrective and preventative actions. Assists engineers in developing methods and procedures to control or improve manufacturing processes.
**MAJOR RESPONSIBILITIES**
+ Assists engineering in providing manufacturing support bylearning to analyse data and identify manufacturing issues and trends. May also train operators on basic processes and engineering changes, and perform operator certification on-the- job training and testing.
+ Assists in identifying manufacturing issues by working withengineering to determine root cause and implementcorrectiveand preventative action.
+ Learns process to disposition non-conforming material byutilising quality tools and by developing knowledge of manufacturing practices andprocedures.
+ Helps to develop and implement process improvements byassisting engineering in researching and validating changes in processes/equipmentandtestmethodstoimproveyieldand/orreduce cycle time per established procedures.
+ Assists engineering in supporting process development duringnewproductintroductionbyprovidinginputtotraceabilityandinspectionrequirements,providinginputforstatisticalprocess control criteria, developing manufacturing instructions, and creating training sheets and certifications.
+ Assists engineering with qualification and validation studies andreports by collecting, compiling, meassuring, organising andrecording data, and by writing procedures. May keeplab notebook.
**EDUCATION & COMPETENCIES**
+ National Framework of Qualifications (NFQ) level 6 qualification in a relevant discipline. 2+ years of related work experience, or an equivalentcombination of education and work experience.
+ Applies broad knowledge of general technical concepts and practices and a general understanding of product or systems fundamentals. Utilises increased knowledge of numerical and statistical data and computer software programs to resolve nonroutine/moderately complex problems. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ Performs non-routine to moderately complex technical assignments using standard methods and sequences. Performs set-up, testing, repair, inspection, and/or maintenance of al I area-specific equipment, materials, systems, and/or product. Makes adjustments, modifications, and replacements as directed. Assignments require broad judgment in troubleshooting proven processes as well as the ability to suggest alternatives.
+ Regularly presents findings to cross-functional teams and begins to win support for ideas. Can adequately write procedures and product disposition documentation that may be presented to external auditing bodies.
+ Mentors new team members. Ensures open communication within group and across shift and relevant functions to resolve technical issues and promote learning.
+ Plans, organises, and prioritises own daily work routine to meet established schedule.
+ Solves a variety of problems of limited to moderate scope and complexity requiring basic interpretation of defined procedures and practices. Maintains confidentiality in handling sensitive information or documents.
+ General supervision. Receives general instruction on routine work and detailed instruction on new assignments.
**REFER TO THE SITE SAFETY STATEMENT (SHE ) FOR YOUR SAFETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
**Abbott Ireland is an Equal Opportunities Employer**
+ Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Ireland Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**PURPOSE OF THE JOB**
Provides technical assistance to engineering to support
manufacturing efforts by implementing corrective and preventative actions. Assists engineers in developing methods and procedures to control or improve manufacturing processes.
**MAJOR RESPONSIBILITIES**
+ Assists engineering in providing manufacturing support bylearning to analyse data and identify manufacturing issues and trends. May also train operators on basic processes and engineering changes, and perform operator certification on-the- job training and testing.
+ Assists in identifying manufacturing issues by working withengineering to determine root cause and implementcorrectiveand preventative action.
+ Learns process to disposition non-conforming material byutilising quality tools and by developing knowledge of manufacturing practices andprocedures.
+ Helps to develop and implement process improvements byassisting engineering in researching and validating changes in processes/equipmentandtestmethodstoimproveyieldand/orreduce cycle time per established procedures.
+ Assists engineering in supporting process development duringnewproductintroductionbyprovidinginputtotraceabilityandinspectionrequirements,providinginputforstatisticalprocess control criteria, developing manufacturing instructions, and creating training sheets and certifications.
+ Assists engineering with qualification and validation studies andreports by collecting, compiling, meassuring, organising andrecording data, and by writing procedures. May keeplab notebook.
**EDUCATION & COMPETENCIES**
+ National Framework of Qualifications (NFQ) level 6 qualification in a relevant discipline. 2+ years of related work experience, or an equivalentcombination of education and work experience.
+ Applies broad knowledge of general technical concepts and practices and a general understanding of product or systems fundamentals. Utilises increased knowledge of numerical and statistical data and computer software programs to resolve nonroutine/moderately complex problems. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ Performs non-routine to moderately complex technical assignments using standard methods and sequences. Performs set-up, testing, repair, inspection, and/or maintenance of al I area-specific equipment, materials, systems, and/or product. Makes adjustments, modifications, and replacements as directed. Assignments require broad judgment in troubleshooting proven processes as well as the ability to suggest alternatives.
+ Regularly presents findings to cross-functional teams and begins to win support for ideas. Can adequately write procedures and product disposition documentation that may be presented to external auditing bodies.
+ Mentors new team members. Ensures open communication within group and across shift and relevant functions to resolve technical issues and promote learning.
+ Plans, organises, and prioritises own daily work routine to meet established schedule.
+ Solves a variety of problems of limited to moderate scope and complexity requiring basic interpretation of defined procedures and practices. Maintains confidentiality in handling sensitive information or documents.
+ General supervision. Receives general instruction on routine work and detailed instruction on new assignments.
**REFER TO THE SITE SAFETY STATEMENT (SHE ) FOR YOUR SAFETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
**Abbott Ireland is an Equal Opportunities Employer**
+ Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
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