102 Quality Assurance jobs in Ireland

Sterility Assurance Specialist

Waterford, Munster Sanofi Group

Job Viewed

Tap Again To Close

Job Description

**Sterility Assurance Specialist**
+ Location: Waterford, Ireland
+ Fixed Term Contract
**About the job**
**About Waterford**
For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.
The Sterility Assurance Specialist will be responsible for developing, implementing, and maintaining sterility assurance programs to ensure compliance with Good Manufacturing Practice (GMP) and regulatory requirements. This role will function as the subject matter expert (SME) for aseptic processing, contamination control, and microbiological quality, supporting manufacturing operations, quality systems, and continuous improvement initiatives.
**Main responsibilities:**
+ Develop, maintain, and improve site sterility assurance strategies and contamination control plans.
+ Lead risk assessments for aseptic processes, cleanroom operations, and sterilisation activities.
+ Ensure compliance with relevant guidelines (e.g., EU GMP Annex 1, FDA Guidance for Industry, ISO standards).
+ Provide SME oversight during aseptic processing, media fills, and environmental monitoring trend reviews. Identifying trends or issues and implementing effective action plans.
+ Support deviation investigations, root cause analysis, and CAPA implementation for sterility-related issues.
+ Review and approve protocols and reports for sterilisation validation, cleanroom qualification, and disinfection studies.
+ Review and approve documentation related to aseptic manufacturing, sterilisation, and microbiological controls.
+ Function as point of contact for sterility assurance during internal and external audits and regulatory inspections.
+ Ensure timely identification and communication of sterility-related risks.
+ Establish and monitor KPIs for the sterility assurance program and report on its performance and effectiveness.
+ Drive improvements in aseptic practices, gowning, cleaning, and contamination control procedures.
+ Deliver training and coaching to manufacturing, QC, and QA teams on sterility assurance principles.
+ Monitor emerging regulatory changes and industry best practices to update site procedures accordingly.
**About you**
+ Bachelor's degree (or higher) in Microbiology, Biology, Pharmacy, or related scientific discipline.
+ Extensive experience in sterility assurance, microbiology, or quality assurance within GMP-regulated manufacturing.
+ Experience leading contamination control strategies and aseptic process validations.
+ Demonstrated track record of successful regulatory inspections.
+ Sterilisation validation experience (e.g., autoclave, VHP, gamma irradiation) desirable.
+ Strong knowledge of aseptic manufacturing, microbiology, sterilisation methods, and cleanroom operations.
+ In-depth understanding of quality and technical regulations in a GMP environment.
+ Analytical mindset with ability to interpret complex microbiological data and environmental monitoring trends.
+ Excellent communication and leadership skills to influence cross-functional teams.
+ Strong problem-solving skills and ability to make decisions under pressure.
**Why choose us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career.
+ Our Waterford site is easily accessible from the M9 and offers excellent facilities including a subsidized restaurant and newly refurbished gym.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
This advertiser has chosen not to accept applicants from your region.

Job No Longer Available

This position is no longer listed on WhatJobs. The employer may be reviewing applications, filled the role, or has removed the listing.

However, we have similar jobs available for you below.

Quality Assurance Engineer

Acuity Brands

Posted 2 days ago

Job Viewed

Tap Again To Close

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 ( (
This advertiser has chosen not to accept applicants from your region.

Quality Assurance Manager

Sligo, Connacht AbbVie

Posted 2 days ago

Job Viewed

Tap Again To Close

Job Description

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are hiring a Quality Assurance Manager to lead our QA team at the Ballytivnan site. This role is responsible for ensuring that all products manufactured at AbbVie meet the requirements of GMP, end users, Regulatory Authorities, and AbbVie standards. The Quality Assurance Manager will oversee team performance, compliance activities, audits/inspections, and serve as a critical partner to operational functions to maintain and improve quality across the site.
Key Responsibilities:
+ Ensure products manufactured at AbbVie meet requirements of end users, Regulatory Authorities, and AbbVie.
+ Lead and manage the Quality Assurance team, providing guidance and support on quality and compliance matters.
+ Act as a site contact for regulatory and customer audits/inspections (FDA, HPRA, etc.) and prepare site teams for successful outcomes.
+ Manage CAPA (Corrective and Preventive Action) implementation, and follow-up activities.
+ Collaborate cross-functionally to resolve quality issues, improve processes, and ensure continuous compliance with cGMP and other relevant regulations.
+ Promote department goals by attracting, developing, and retaining capable QA staff.
+ Contribute to talent management and professional development of QA personnel.
+ Develop, review, and approve QA documentation as related to general QA activities.
+ Provide oversight of batch record review, deviation investigations, change controls, and product release decisions.
+ Support quality meetings and key quality metrics and trends.
+ Communicate effectively with internal and external stakeholders, including the AbbVie Quality and Compliance Group and regulatory bodies.
+ Serve as a designee for the Biologics Quality Director as required.
Qualifications
+ Bachelor's degree in science, Quality, Engineering, or related field (Master's preferred)
+ Minimum of 8 years' experience in the healthcare, pharmaceutical, or biopharmaceutical industry
+ At least 3 years' supervisory/people management experience
+ Demonstrated experience with audits and/or inspections (FDA, HPRA, etc.)
+ High level of expertise in day-to-day quality and compliance decision-making
+ In-depth knowledge of GMP requirements and regulatory frameworks
+ Strong attention to detail and commitment to compliance and quality standards
+ Ability to facilitate quality decision-making while maintaining a strong patient focus and upholding AbbVie's reputation
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.

Quality Assurance Analyst

Cork, Munster Clearstream Fund Centre S.A., Cork Branch

Posted 1 day ago

Job Viewed

Tap Again To Close

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.

Quality Assurance Specialist

Dublin, Leinster Recruitment by Aphex

Posted 3 days ago

Job Viewed

Tap Again To Close

Job Description

Purpose An exciting opportunity has arisen for a Quality Assurance Specialist to join our team. The role ensures that the QA team objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers, as well as meeting Health Agency regulations and all other applicable governing regulations. This position will report directly to the Quality Assurance COE Lead. Requirements Support various site functional and cross-functional tier structures. Completes review and approval for CAPAs, change requests, investigative protocols, and final reports. Responsible for the quality aspects of material and supplier management, such as compilation of material qualification pack, supplier audit review, and supplier management system upkeep. Involved in the development and review of documentation and quality records in collaboration with other stakeholders such as QC, MS&T, Engineering, and Warehouse throughout the product lifecycle e.g., method validation, facility upgrades, qualification protocols, calibration records. Review and approve GMP documentation/data for accuracy and completeness. Working cross-functionally to ensure project milestones are met in a timely manner. Collaborates with cross-functional team members in the identification and implementation of continuous improvement initiatives and action plans. A self-starter and results-focused, the successful candidate will have strong contemporary knowledge of relevant cGMPs, regulations and current industry trends. Strong collaboration and cross-functional leadership skills. Strong verbal and written communication skills, project management skills. Requirements Bachelor's degree (or higher) in Chemistry, Biology, Microbiology, Engineering or Supply Chain in a relevant discipline. 5 years' experience in Quality Control, Quality Assurance or Pharmaceutical, Vaccine or Biological Operations, or Technical Operations. 2 years of experience in performing the release function in a regulated environment Strong knowledge of qualification and implementation of single-use technologies and raw materials for use in a GMP environment. Strong contemporary knowledge of relevant cGMPs, regulations, and current industry trends. Proven track record in delivering excellence. Knowledge of SAP, KNEAT, and Veeva systems is an advantage. Skills: SAP KNEAT CAPA Document Review
This advertiser has chosen not to accept applicants from your region.

Quality Assurance Specialist

Dublin, Leinster Life Science Consultants (LSC)

Posted 4 days ago

Job Viewed

Tap Again To Close

Job Description

LSC have a great opportunity for a Senior QA Specialist to join a South Dublin-based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 7+ years of experience in construction management/engineering within the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Act as Quality point of contact and decision maker during New Product Introductions, Technology Transfer and Process Validation activities for Aseptic products Quality review and approval of Process Development and Validation documentation Technical transfer documents Validation Protocols, executed validation documents and reports Provide Quality direction and input at Change Control and Deviation Review Boards and assume QA oversight of change control and Deviation/CAPA records ABOUT YOU - ARE YOUR SKILLS A MATCH? Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G visa or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship. Thank you for your understanding. Apply via this advert or contact Siobhan Cummins on if you have any more questions about this opportunity!
This advertiser has chosen not to accept applicants from your region.

Quality Assurance Manager

Dundalk, Leinster Hunter Savage

Posted 17 days ago

Job Viewed

Tap Again To Close

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.

Quality Assurance Technician

Monaghan, Ulster Hunter Savage

Posted today

Job Viewed

Tap Again To Close

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.
Be The First To Know

About the latest Quality assurance Jobs in Ireland !

Quality Assurance Technician

Monaghan, Ulster Vickerstock UK

Posted today

Job Viewed

Tap Again To Close

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.

Quality Assurance Technician

Dublin, Leinster Hunter Savage

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Title: Quality Assurance Technician Location: Lusk, Co. Dublin Reports To: Technical Manager A well-established fresh-produce manufacturer is seeking a Quality Assurance Technician to join its busy Quality team. In this role you will support the Technical Management team to ensure all products meet the highest standards of food safety, quality, and compliance with Irish and EU regulations. You will work closely with production staff to monitor, test, and continuously improve processes so that customer expectations and statutory requirements are consistently achieved. Key Responsibilities Verify that all produce is processed, prepared, and packaged to agreed specifications and quality standards. Check quantities, labelling, and packaging to meet both functional and presentation requirements. Work alongside production to ensure ongoing compliance with food safety legislation, customer specifications, and industry standards (HACCP, FSAI guidelines, EU regulations). Lead root-cause analysis for any non-conformance or quality issues. Implement and document Corrective and Preventive Actions (CAPA), updating SOPs, training staff, and adjusting production techniques as required. Conduct routine tests and inspections of incoming raw materials and finished goods, including sensory, microbiological, and shelf-life assessments. Use statistical sampling to maintain consistency and address variations promptly. Oversee cleaning and sanitation procedures across production areas. Carry out environmental swabbing and monitor critical areas to prevent microbial contamination. Monitor and record temperatures throughout storage, processing, and distribution to maintain product quality and food safety. Ensure all processing procedures meet internal standards and comply with HACCP, GMP, and the latest Irish/EU food safety regulations. Keep up to date with changes in food safety legislation and industry best practice. Qualifications & Experience Previous experience in food manufacturing or quality assurance, ideally within fresh produce. Solid knowledge of Irish food safety standards, HACCP, GMP, and FSAI guidelines. Competence in inspection techniques and use of relevant laboratory tools. Excellent organizational skills and attention to detail. This is an excellent opportunity for an experienced Quality professional to join a dynamic food manufacturing environment and play a key role in maintaining exceptional product standards.
This advertiser has chosen not to accept applicants from your region.

Quality Assurance Technician

Dublin, Leinster Vickerstock UK

Posted today

Job Viewed

Tap Again To Close

Job Description

Quality Assurance Technician North Dublin Full-time/Permanent Day & Evening Shift Attractive Salary + Company Bonus & Benefits Vickerstock are working in partnership with our Irish client who are fresh food manufacturers located in North Dublin. Supplying products to both retail and food service sectors across Ireland. Reporting to the Quality Manager you will ensure day to day production operations are conducted in a quality focused way. This will involve meeting deadlines and ensuring both Food Safety and Customer Quality standards are maintained. Key duties Be a proactive member of the Quality Assurance Team to ensure all products produced comply with all Food safety quality and legislative requirements. Ensure preparation, portioning and packing of food products is done according to established standards and customer specifications Implementing corrective action programs for any non-conformances raised Plan, conduct and monitor testing and inspection of raw materials and products Carrying out product and process validations Ensuring all production and quality paperwork are filled correctly and comply with all food safety standards and legislation Carry out calibration checks on equipment in the factory such as temperature probes, data loggers and scales Monitor and verify cleaning processes in the factory Carry out internal audits Experience Required Minimum 1 year experience within Quality department in Food Manufacturing/FMCG Ideally 3rd level qualification in relevant discipline Full driving licence and access to car (factory is not accessible by public transport so you must drive) In return you will receive Attractive salary Annual company bonus 20 days annual leave Free meals on site Continuous career development Bike to work scheme Retail discount card 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 Quality Technician QA Technician Quality
This advertiser has chosen not to accept applicants from your region.
 

Nearby Locations

Other Jobs Near Me

Industry

  1. request_quote Accounting
  2. work Administrative
  3. eco Agriculture Forestry
  4. smart_toy AI & Emerging Technologies
  5. school Apprenticeships & Trainee
  6. apartment Architecture
  7. palette Arts & Entertainment
  8. directions_car Automotive
  9. flight_takeoff Aviation
  10. account_balance Banking & Finance
  11. local_florist Beauty & Wellness
  12. restaurant Catering
  13. volunteer_activism Charity & Voluntary
  14. science Chemical Engineering
  15. child_friendly Childcare
  16. foundation Civil Engineering
  17. clean_hands Cleaning & Sanitation
  18. diversity_3 Community & Social Care
  19. construction Construction
  20. brush Creative & Digital
  21. currency_bitcoin Crypto & Blockchain
  22. support_agent Customer Service & Helpdesk
  23. medical_services Dental
  24. medical_services Driving & Transport
  25. medical_services E Commerce & Social Media
  26. school Education & Teaching
  27. electrical_services Electrical Engineering
  28. bolt Energy
  29. local_mall Fmcg
  30. gavel Government & Non Profit
  31. emoji_events Graduate
  32. health_and_safety Healthcare
  33. beach_access Hospitality & Tourism
  34. groups Human Resources
  35. precision_manufacturing Industrial Engineering
  36. security Information Security
  37. handyman Installation & Maintenance
  38. policy Insurance
  39. code IT & Software
  40. gavel Legal
  41. sports_soccer Leisure & Sports
  42. inventory_2 Logistics & Warehousing
  43. supervisor_account Management
  44. supervisor_account Management Consultancy
  45. supervisor_account Manufacturing & Production
  46. campaign Marketing
  47. build Mechanical Engineering
  48. perm_media Media & PR
  49. local_hospital Medical
  50. local_hospital Military & Public Safety
  51. local_hospital Mining
  52. medical_services Nursing
  53. local_gas_station Oil & Gas
  54. biotech Pharmaceutical
  55. checklist_rtl Project Management
  56. shopping_bag Purchasing
  57. home_work Real Estate
  58. person_search Recruitment Consultancy
  59. store Retail
  60. point_of_sale Sales
  61. science Scientific Research & Development
  62. wifi Telecoms
  63. psychology Therapy
  64. pets Veterinary
View All Quality Assurance Jobs