286 Manufacturing Quality jobs in Ireland
Manufacturing Quality Engineer
Posted today
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Job Description
We're looking for a hands-on manufacturing quality engineer who thrives on solving problems - not just reporting them. This is a practical, on-the-floor role supporting the production of high performance heating systems used across Europe.
You'll work with R&D to launch new products, lead ISO audits, troubleshoot quality issues, and implement real changes on the ground. One day you're breaking down problems with suppliers; the next, you're improving processes or rolling out component changes.
Experience in manufacturing and ISO is essential. Sheet metal and electrical assembly knowledge (cables, crimping, LEDs) is a big plus. AutoCAD Inventor and Excel required.
This role suits someone who doesn't want to sit behind a desk all day—someone who owns issues, drives improvements, and follows through.
Specific Skills / Expectations for the right candidate:
Manufacturing Engineering
Work with R&D and Production to assist with New Product Introductions
Manage Engineering Change Notices
Technical Liaison with suppliers
Create Work Instructions and Procedures for Manufacturing Tasks.
Organise external Maintenance Contractors
Preventive Maintenance Schedule
Manage Bills of Material
Seek and Implement Product Cost Reduction Opportunities
Safety, carry out audits, attend meetings, close out actions.
Work toward 5S implementation.
Quality Engineering
ISO Audits
Collect Quality Data and prepare for presentation to Senior Management
Work with Customer Service to identify patterns in calls.
Update Procedures and Policies
Create and Close Out Corrective Action Reports
Manage Supplier Returns and Credits
Liaison to suppliers on Quality Issues
Host Quality Meetings.
Maintain Quality KPIs
Write Specific Quality Reports when required
Skills:
Autocad Excel ISO 9001 Iso 9000 Manufacturing Sheet Metal Electrical
Manufacturing/Quality Engineer
Posted today
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Job Description
Are you a Quality/Manufacturing engineer looking for a new opportunity? Don't hesitate and apply today
PROJECT DESCRIPTION
We are seeking experienced Remediation Quality Engineers / Manufacturing Engineers to support a site-wide remediation program following an FDA 483. These roles will focus on manufacturing process validation, quality system updates, and documentation remediation. Consultants will be based onsite and work directly with manufacturing and quality process owners to identify compliance gaps, implement corrective actions, and ensure documentation is accurate and audit-ready.
The project will involve tackling remediation areas in sequence, updating technical files and procedures, and ensuring robust validation of manufacturing processes. Consultants must be able to take a problem statement through to a compliant solution, collaborating cross-functionally across Quality, Manufacturing, and Regulatory teams.
PROJECT DESCRIPTION
- Partner with process owners on the floor to capture and remediate issues.
- Support process validation (IQ/OQ/PQ) and documentation updates.
- Drive CAPA/NCR closure and implement compliant solutions.
- Provide technical writing for quality and manufacturing documents.
- Collaborate cross-functionally to ensure regulatory compliance.
CONSULTANT RESPONSIBILITIES
- Engineering or Quality degree with 5-10 years' med-tech experience.
- Background in remediation, process validation, CAPA, NCRs.
- Strong technical writing and documentation skills.
- Knowledge of 21 CFR Part 820, ISO 13485.
Senior Manufacturing Quality Engineer
Posted today
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Job Description
Cohesity is the leader in AI-powered data security. Over 13,600 enterprise customers, including over 85 of the Fortune 100 and nearly 70% of the Global 500, rely on Cohesity to strengthen their resilience while providing Gen AI insights into their vast amounts of data. Formed from the combination of Cohesity with Veritas' enterprise data protection business, the company's solutions secure and protect data on-premises, in the cloud, and at the edge. Backed by NVIDIA, IBM, HPE, Cisco, AWS, Google Cloud, and others, Cohesity is headquartered in Santa Clara, CA, with offices around the globe.
We've been named a Leader by multiple analyst firms and have been globally recognized for Innovation, Product Strength, and Simplicity in Design , and our culture.
Want to join the leader in AI-powered data security?
Cohesity is seeking a
Senior Manufacturing Quality Engineer
responsible for driving manufacturing quality excellence across the server/storage product portfolio. The ideal candidate will focus on developing and sustaining quality processes across the product lifecycle—from NPI to production—ensuring robust box build process controls, supplier quality, and issue resolution. This individual will work closely with hardware engineering, manufacturing, test engineering, supplier quality, and supply chain teams. This full-time position reports to the Manager of Quality Engineering within the Operations Engineering organization.
How You'll Spend Your Time Here
- Own and improve quality processes across manufacturing lines (system assembly, test, packaging, etc.)
- Lead root cause analysis and drive corrective/preventive actions (RCCA) on manufacturing quality escapes, yield issues, and process deviations.
- Monitor in-line quality metrics and yield data; identify trends and proactively drive continuous improvement.
- Support NPI builds by establishing quality inspection plans, control plans, and incoming inspection criteria.
- Collaborate with OEM/ODM/CM partners to ensure adherence to quality standards and process capability requirements.
- Lead regular quality reviews with manufacturing partners and internal stakeholders to align on metrics, priorities, and actions.
- Perform audits (internal and supplier) to assess quality system compliance and drive closure of any non-conformities.
- Partner with test and engineering teams to qualify new processes, fixtures, and equipment from a quality standpoint.
- Manage and maintain the manufacturing quality documentation (e.g., Specs., Control Plans, Quality Alerts).
- Be the first point of contact for any factory quality issues.
- Drive measurable improvements in production yields, defect rates, and manufacturing quality metrics.
- Deliver high-quality NPI launches with robust quality plans and minimal escapes.
- Be a key interface between engineering and manufacturing on quality-related topics.
- Foster a culture of continuous improvement with internal and external manufacturing teams.
WE'D LOVE TO TALK TO YOU IF YOU HAVE MANY OF THE FOLLOWING:
- Strong knowledge of PCBA and system-level manufacturing processes, quality controls, and test methodologies.
- Experience with quality engineering tools (e.g., 8D, 5Whys, Fishbone, FMEA, DMAIC, SPC analysis).
- Working knowledge of manufacturing quality standards (e.g., ISO 9001, IPC-A-610).
- Hands-on experience collaborating with contract manufacturers and suppliers, preferably in the server/storage industry.
- Excellent data analysis and reporting skills (Excel, Tableau, SQL or other BI tools).
- Exceptional problem-solving and communication skills across cross-functional teams.
- Flexibility to support builds in multiple time zones and in a fast-paced product ramp environment.
- Demonstrated ability to leverage AI tools to enhance productivity, streamline workflows, and support decision making
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**Equal Employment Opportunity Employer (EEOE)
Cohesity is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex, sexual orientation, national origin or nationality, ancestry, age, disability, gender identity or expression, marital status, veteran status or any other category protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact us at COHESITY or
for assistance.
In-Office Expectations
Cohesity employees who are within a reasonable commute (e.g. within a forty-five (45) minute average travel time) work out of our core offices 2-3 days a week of their choosing.
Interested candidates based outside of the designated areas are welcome to apply, provided they have the right to work in the job location.
Manufacturing Engineer/Quality Engineer
Posted 19 days ago
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Job Description
At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.
**Abbott Ireland**
In Ireland, Abbott employs over 6,000 people across ten sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**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.
**We are currently looking for Manufacturing Engineers and Quality Engineers to join our modern site in Clonmel.**
**This is how you will make a difference:**
As a Manufacturing Engineer, you will be responsible for engineering support of manufacturing operations, which will involve key engineering metric management and process optimization activities including Manufacturing Yield improvement, product quality monitoring, lean manufacturing design and material/equipment/process troubleshooting using continuous improvement tools and methodology. Working as part of the operations support team, the manufacturing engineer will liaise with operations, quality, R&D and materials & purchasing departments to ensure quality and efficient manufacturing operations.
**Main responsibilities**
+ Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company.
+ Prepares reports, publishes, and makes presentations to communicate findings.
+ Analyses and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology.
+ Understands engineering principles theories, concepts, practices and techniques.
+ Understands the business needs of the company, and has knowledge of the customer needs of our business.
+ Understands the business cycle and foresight of emerging technologies trends.
+ Cultivates internal and external network of resources to complete tasks. Serves as a resource in the selection orientation and training of new engineers and employees.
+ May lead a project team, determining goals and objectives for the projects.
+ Mentors employees by sharing technical expertise and providing feedback and guidance.
+ Interacts cross functionally and with internal and external customers.
+ Serves as a consultant for engineering or scientific interpretations and advice on significant matters.
+ Acts as a spokesperson to customers on business unit current and future capabilities.
+ Participates in validation activity. Role may vary between providing input to owning activities such as protocol/report writing and managing execution of validation activities.
**Experience, Education and Skills Required - Manufacturing Engineer:**
+ National Framework of Qualifications (NFQ) level 7 qualification in a relevant discipline.2+ years of related work experience, or an equivalent combination of education and work experience.
+ Basic technical knowledge of concepts, practices and procedures. Limited understanding of business unit/group function.
+ Learns to use professional concepts and company policies and procedures to solve routine problems.
+ Developing a network of internal resources to facilitate completion of tasks.
**JOB DESCRIPTION:**
**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.
**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 Statement:**
Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products.
Shift Role: 2-cycle shift (8-16:30 and 16:30-00:30)
**Key Responsibilities - Quality Engineer:**
1. Identifies manufacturing process defects (scrap, non-conforming material, customer complaints) by dispositioning non-conforming material, identifying primary root causes and suggesting corrective and preventative actions. May be responsible for querying and bounding data to support implementation of basic product stops.
2. Assists in development of product quality plans, documents and systems by providing input to product specifications, quality specifications, quality plans, risk analyses, Failure Mode Effect Analysis (FMEA) in conjunction with other product development team members. May be responsible for providing input to risk analyses and Failure Mode Effect Analysis' (FMEAs).
3. Becomes skilled at using process monitoring systems by starting to identify critical process steps and applying basic methods to reduce process variation to reduce/eliminate the cause of defects.
4. Assists product/process improvement efforts (example, scrap, nonconforming product, customer complaints) by systematically gathering quality metric data based on previous program templates and by assisting in the appropriate analysis methods to enhance sustaining product design and new product development.
5. Becomes skilled at using quality tools and training materials by working with existing quality tools and training materials and by understanding evolution/history of tools in use.
6. Participates in validation activity. Role may vary between providing input to owning activities such as protocol/report writing and managing execution of validation activities.
7. Participates in corrective and preventive action activity.
8. Participates in Field Discrepancy Notification (FDN) investigations.
**Education & Job Skills - Quality Engineer**
+ (Education/ Experience) National Framework of Qualifications (NFQ) level 7 qualification in a relevant discipline. 2+ years of related work experience, or an equivalent combination of education and work experience.
+ (Technical/Business Knowledge (Job Skills)) Working technical knowledge and application of concepts, practices and procedures. General understanding of business unit/group function. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ (Cognitive Skills) Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. Has a broad knowledge of technical alternatives and an understanding of their impact on the systems environment.
+ (Influence/Leadership) Cultivates a wide range of internal networks and begins to develop an extensive external network of resources to facilitate completion of tasks. May lead a project team of moderate scope. Provides guidance to less experienced staff. Acts as a mentor to lower level individual contributors. Influence exerted at peer level and occasionally at first levels of management.
+ (Planning/Organisation) Plans, organises, and prioritises own daily work routine to meet established schedule.
+ (Decision Making/Impact) Exercises authority and judgment within defined limits to determine appropriate action. Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources.
+ (Supervision Provided) May provide limited work direction and guidance to exempt and/or skilled nonexempt levels of employees, may be asked to evaluate performance of and assist in career development planning for subordinates.
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
Quality Assurance Quality Control Engineer
Posted today
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Job Description
About
My client is a leading provider of electrical engineering solutions for a wide range of industry sectors including Data Centres, Pharmaceutical, Commercial, and Industrial sectors across Europe. With a focus on innovation, safety, and quality, my client delivers complex projects on time and to the highest standards.
Role Overview
As a QA/QC Engineer, you will play a critical role in ensuring that all aspects of project execution meet both client and regulatory quality requirements. You will be responsible for implementing the QA/QC procedures, inspecting installations, and managing quality documentation across all phases of the project lifecycle.
Key Responsibilities
- Implement and maintain the Project Quality Plan (PQP) and Inspection Test Plans (ITPs).
- Carry out inspections and quality checks on electrical/mechanical installations in accordance with project specifications, standards, and regulations.
- Ensure all works are carried out in line with the latest approved drawings and documentation.
- Monitor subcontractor and supplier quality performance.
- Record and track non-conformances and coordinate corrective actions.
- Assist in the development and execution of method statements and quality documentation.
- Conduct material inspections and verify compliance with project requirements.
- Participate in internal and external audits.
- Prepare quality-related reports, snag lists, and handover documentation (e.g., Inspection & Test Records, O&M Manuals).
- Liaise with the Project Management team, Client QA/QC Representatives, and third-party inspectors.
Requirements
Education & Qualifications
- Degree/Diploma in Electrical, Mechanical, Building Services, or related engineering discipline.
- ISO 9001 Lead Auditor (desirable).
Experience
- 2–5+ years of QA/QC experience in a construction or MEP environment (data centre experience is a strong advantage).
- Experience with QA/QC systems and tools, including check sheets, ITPs, and NCR processes.
- Qualified Electricians comfortable with tablets/laptops or Electrical Engineers experienced in building test packs
Skills & Competencies
- Strong attention to detail and analytical skills.
- Knowledge of applicable standards (e.g., ISO, IEC, BS EN).
- Familiarity with industry-standard software (e.g., Bluebeam, Procore, Navisworks, AutoCAD, BIM tools).
- Excellent communication and reporting skills.
- Ability to work independently and as part of a multi-disciplinary team.
Benefits
- Competitive salary based on experience.
- Opportunity to work on high-profile international projects.
- Career development and training support.
- Travel and accommodation support (where applicable).
- Dynamic and inclusive work environment.
Quality Assurance
Posted today
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Job Description
JARU is a dynamic and growing food business with operations across a production kitchen, restaurant, and food market. We are committed to delivering high-quality retail food products while maintaining the highest hygiene and safety standards. We're currently seeking a Quality Assurance Specialist to join our team and oversee food safety, hygiene, and compliance practices across all our locations.
Key Responsibilities
- Work closely with the production kitchen team to ensure all retail products meet food safety and quality standards
- Manage and maintain the HACCP system, including documentation and implementation across the production kitchen, restaurant, and food market
- Monitor hygiene records and ensure full compliance with food safety regulations and company standards
- Conduct regular audits across all sites (production kitchen, restaurant, and food market)
- Train and support kitchen staff in food safety procedures and hygiene best practices
- Identify risks and areas for improvement, and implement corrective actions
- Liaise with health and safety authorities and external auditors as needed
Requirements
- Minimum 5 years of kitchen experience, ideally in a supervisory or quality-focused role
- Strong understanding of HACCP, food safety regulations, and hygiene standards
- Excellent organizational and documentation skills
- Confident in conducting audits and addressing non-conformities
- Able to work independently and collaboratively across different teams
- Fluent in English (spoken and written)
Desirable (but not essential)
- EU Category B (van) driving license – for site visits and audits
- Previous experience in a QA or compliance role within the food industry
- Knowledge of local food safety legislation and inspection processes
What We Offer
- Opportunity to play a key role in a growing food business
- Collaborative work environment with a focus on quality and innovation
- Staff discounts, meals on duty, on-site parking
Job Type: Full-time
Pay: From €17.00 per hour
Benefits:
- Employee discount
- On-site parking
- Sick pay
Work Location: In person
Senior Quality Assurance – Plant Technical Quality Assurance
Posted today
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Job Description
Purpose
The Plant Technical Quality Assurance (PTQA) Specialist is a senior position within the QA function which will typically report to a QA Manager and will be required to be a Subject Matter Expert in their assigned area of responsibility.
Responsibilities
• Act as Quality point of contact and decision maker during New Product Introductions, Technology Transfer and Process Validation activities for Aseptic products, ensuring that all activities meet Client and regulatory expectations.
• Quality review and approval of Process Development and Validation documentation
o Technical transfer documents
o 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; ensuring scope of record is clear and implementation activities are robust and timely.
• Perform all activities in compliance with Client safety standards and SOPs
In line with business requirements, these responsibilities may expand or otherwise include additional areas of responsibility which are not described in this specification but are associated with the role
Requirements
• University degree. Science or Engineering related discipline preferred.
• Understanding of principles of Validation and New Product Introduction
• Experience in aseptic manufacturing
• Relevant experience (7yrs +) working in the pharmaceutical or biotechnology industry as a Subject Matter Expert providing overall quality direction and oversight for key functional areas (i.e. Process Development, Validation, Manufacturing)
• Experience in change control, non-conformance, corrective and preventative actions, and validation practices.
• Ability to operate across functional boundaries, both internal and external.
• Ability to work independently and remotely with minimum direct supervision.
• Critical thinking skills.
• Strong organisational, communication, coordination, and meeting facilitation skills.
• Independent, self-motivated, organized, able to multi-task in project environments and skilled in communication and collaboration.
• Team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
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ADSEO Quality Assurance
Posted today
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Global Operations
ADSEO Quality Assurance - French (12 Month Fixed-Term Contract)
Location
:
Dublin
Employment Type
:
Regular
Job Code
:
A
Responsibilities
Our Trust & Safety team's commitment is to keep our online community safe. We have invested heavily in human and machine-based moderation to remove harmful content quickly and often before it reaches our general community.
Our QA's will take ownership of the quality success of their internal or external stakeholders, identify and clear blockers to high performance, and be on hand to support their team in their drive for excellence. They will take an active role in performance monitoring, and provide crucial reporting to relevant stakeholders, leading to the success & growth of our teams.
The successful candidate must be capable of working with XFN teams to identify the needs of their project. Be comfortable navigating ambiguous situations, and be able to set clear SMART goals for themselves & our teams.
They must also be willing and able to take ownership of this role, identify & suggest process improvements, & help to develop a best practice methodology for the QA role.
Content that QA interacts with includes images, video, and text related to every-day life, but it can also include (but is not limited to) bullying; hate speech; child safety; depictions of harm to self and others, and harm to animals.
What will I be doing:
- Working both independently, and in collaboration with stakeholders, to deliver high performance standards across all relevant projects, and develop a best practice model for maintaining high performance on those projects.
- Facilitate regular calibration meetings with stakeholders to maintain knowledge & quality standards, and provide feedback on implementation and execution.
- Work closely with the Policy POC to disseminate policy updates and knowledge to your teams, and facilitate efficient & timely communication of policy questions between all internal & external stakeholders.
- Perform daily audits and provide analysis of errors and feedback to respective teams.
- Compile & deliver regular performance data reports to SME & management teams as required.
- Conduct regular RCA escalations through the relevant process.
- Identify and assess areas for performance improvement across relevant markets, and be solution driven and proactive in delivering these solutions.
- Participate in or lead policy briefings to ensure any changes are consistent and in line with current cultural, socio, geographical and political conditions.
- Balance efficient delivery of tasks in each queue through relevant platforms such as TCS or Rock Appeal.
- Be able & willing to support or backfill temporary gaps in market support.
- Be able to support the internal onboarding team to further develop onboarding training SOP's & materials, as well as ongoing legacy planning.
- Perform regular queue moderation, or participate in knowledge quizzes when required, to maintain policy implementation skills.
- Design/help to design a training plan and implement it according to the timeline
- Please note that this position involves exposure to sensitive content, including but not limited to vulgar content, violence, pornography, and fake news.
Qualifications
Minimum Qualifications
- Minimum 1-year QA or relevant experience in trust and safety or policy in a major tech or media company.
- Demonstrate a broad understanding of our business needs, strategic thinking skills and ability to make good decisions in complex situations.
- Familiar with the business logic of labeling and working mode of the upstream and downstream teams.
- Fluency in French is required as the role requires communication with French markets, fluency in English is also required as it is the working language.
- Comfortable reporting to, or collaborating with, a broad range of XFN partners.
- A fast learner who has the ability to embrace a fast-paced working environment.
Preferred Qualifications
- Bachelor's degree and above or equivalent working experience in a short video product user industry.
- Experience in Content Moderation/Content Quality/Content Safety/Labeling will be an added advantage.
- Familiarity with Microsoft Office Suite (PPT / Excel / Word).
- Familiarity with machine learning and content understanding.
- Solid presentation, communication and interpersonal skills.
Job Information
About TikTok
TikTok is the leading destination for short-form mobile video. At TikTok, our mission is to inspire creativity and bring joy. TikTok's global headquarters are in Los Angeles and Singapore, and we also have offices in New York City, London, Dublin, Paris, Berlin, Dubai, Jakarta, Seoul, and Tokyo.
Why Join Us
Inspiring creativity is at the core of TikTok's mission. Our innovative product is built to help people authentically express themselves, discover and connect – and our global, diverse teams make that possible. Together, we create value for our communities, inspire creativity and bring joy - a mission we work towards every day.
We strive to do great things with great people. We lead with curiosity, humility, and a desire to make impact in a rapidly growing tech company. Every challenge is an opportunity to learn and innovate as one team. We're resilient and embrace challenges as they come. By constantly iterating and fostering an "Always Day 1" mindset, we achieve meaningful breakthroughs for ourselves, our company, and our users. When we create and grow together, the possibilities are limitless. Join us.
Diversity & Inclusion
TikTok is committed to creating an inclusive space where employees are valued for their skills, experiences, and unique perspectives. Our platform connects people from across the globe and so does our workplace. At TikTok, our mission is to inspire creativity and bring joy. To achieve that goal, we are committed to celebrating our diverse voices and to creating an environment that reflects the many communities we reach. We are passionate about this and hope you are too.
Trust & Safety
TikTok recognises that keeping our platform safe for the TikTok communities is no ordinary job which can be both rewarding and psychologically demanding and emotionally taxing for some. This is why we are sharing the potential hazards, risks and implications in this unique line of work from the start, so our candidates are well informed before joining.
We are committed to the wellbeing of all our employees and promise to provide comprehensive and evidence-based programs, to promote and support physical and mental wellbeing throughout each employee's journey with us. We believe that wellbeing is a relationship and that everyone has a part to play, so we work in collaboration and consultation with our employees and across our functions in order to ensure a truly person-centred, innovative and integrated approach.
Quality Assurance Manager
Posted today
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Job Description
Quality Manager – Award-Winning Food Manufacturer
An award-winning Irish food manufacturing company, renowned for its commitment to excellence and innovation, is seeking a
Quality Manager
to join its growing team. With a reputation for producing high-quality products using the finest ingredients, the business prides itself on maintaining the highest standards of food safety, quality, and compliance.
About the Role:
This leadership role is central to ensuring that all products consistently meet food safety, regulatory, and customer requirements. You will oversee all aspects of quality management and technical compliance across the site.
What we offer:
- Location: Co. Cavan
- Working Hours: Monday to Friday, 8:00am-4:30pm (No Weekends)
- Salary: €50'000 DOE
- Full-Time Permanent Position
Key Responsibilities
- Lead and manage the company's Quality Management System, ensuring compliance with HACCP, BRC, and customer standards.
- Coordinate and conduct internal audits, staff training, and site inspections.
- Oversee product quality and food safety, including the review and approval of labels and artwork in line with food legislation.
- Investigate customer complaints, identify trends, and drive corrective and preventative actions.
- Act as the primary contact for external audits and regulatory inspections.
- Monitor production performance and implement continuous improvement initiatives.
- Manage environmental testing programmes and ensure ongoing compliance.
- Support Health & Safety activities throughout the business.
- Stay current with changes in food safety legislation and update systems accordingly.
About You
- Food Science Degree or Degree in a related field.
- Proven experience in a quality or technical management role within the food manufacturing sector.
- Strong knowledge of HACCP, BRC, and relevant food legislation.
- Excellent leadership, communication, and problem-solving skills.
- Ability to manage multiple projects, prioritise effectively, and meet deadlines.
Apply Today
Quality Assurance Specialist
Posted today
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Job Description
Quality Assurance Senior Specialist (Contract – Dundalk, On-site)
Pay Rate:
€29.44/hr – €52.05/hr
We are seeking a
QA CSQ/CQV Specialist (Contractor/Consultant)
to provide oversight of validation activities, ensuring compliance with cGMP, regulatory requirements, and SOPs. This role supports commissioning, qualification, and validation (CQV) activities during facility start-up and transition to commercial operations.
Key Responsibilities
- Provide QA oversight of validation/qualification activities for facilities, utilities, equipment, computerized systems, cleaning, processes, storage areas, CTUs, and shipping.
- Review and approve validation documentation (URS, risk assessments, protocols, reports) to ensure compliance with SOPs and acceptance criteria.
- Ensure deviations, investigations, and change controls during validation activities are properly managed with QA oversight.
- Review SOPs related to qualification/validation activities.
- Support audits, regulatory inspections, and ensure validation readiness.
- Maintain compliance with EU/FDA cGMP, ISO, and industry standards (GAMP, ISPE, ASME, BPE).
- Coordinate QA validation activities to meet project timelines.
- Manage and support QA validation team performance, recruitment, and training.
Qualifications & Experience
- B.Sc. or B.Eng. in Science or Engineering (e.g., Biochemistry, Chemistry, Engineering).
- Experience in QA/Validation in biologics, pharma, or medical device manufacturing (FDA/EU regulated).
- Strong knowledge of validation requirements in cGMP environments.
- Familiar with root cause analysis tools (Ishikawa, FMEA, 5 Whys).
- Strong planning, problem-solving, and critical thinking skills.
- Ability to work independently in a fast-paced, cross-functional environment.
Niche Skills (Preferred/Recommended)
- CQV Oversight
– commissioning & qualification for start-up facilities. - Validation Expertise
– facilities, utilities, equipment, cleaning, computerized systems. - Regulatory Knowledge
– EU GMP Annex 15, FDA 21 CFR Part 11, ISO, GAMP 5. - Quality Systems
– deviations, CAPA, change control, audit readiness. - Risk Management Tools
– FMEA, Ishikawa, fault tree analysis. - Technical Documentation
– URS, validation master plans, IQ/OQ/PQ protocols.