What Jobs are available for Quality Control in Cork?

Cairn Homes has a unique opportunity for a Quality Control Supervisor to join our growing team, in a fast-paced dynamic working environment. This is a multi-site role that requires ongoing quality inspections across all of Cairn apartment and housing sites based on a weekly inspection schedule.

Key responsibilities;

Typically, the candidate will be expected to undertake and assist with the following duties across the full portfolio of Cairn live sites.

• Undertake daily walkthrough Inspections of all Cairn Homes operational sites to identify and report any compliance or defect issues relating to ongoing works.
• Travel to Cairn Sites (Predominantly in the Cork Region) based on a weekly schedule set and agreed by our supervisor lead.
• Attend nominated site activities where required, e.g. meetings, whiteboards etc
• Ensure that all Cairn quality procedures are understood and are being followed by the Cairn Site Teams & Subcontractors
• Build and develop strong working relationships with Cairn Site Teams including Project and Site Managers.
• Proactively investigate building defects or issues of concern relating to quality when identified during site inspections
• Input quality data and monthly reports into Cairn's construction software platform. (Training provided on our system as part of the onboarding)
• Conduct a verbal debrief with the Site Manager or nominated contact, discuss key observations, recurring issues, and immediate actions.
• Continually develop your quality expertise to increase your knowledge, and expertise in Quality activities, building regulations and best practices through training courses and CPD. (Cairn provide a training allowance & professional subscriptions / fees for all employees).
• Work within a collective team environment that creates a quality culture that supports high employee morale
• Undertake such other tasks as may be reasonably requested by your Manager.

The candidate

• Background in large scale, residential construction with emphasis on Apartments and housing developments
• Trades background with appropriate certification (preferable)
• 5 + years' experience in a similar role
• Knowledge of typical construction details and good working knowledge of latest building regulations
• Excellent communication skills
• To be methodical, pay attention to detail and be inquisitive challenging site teams.
• To be good at working with people at all levels and willing to work in a team.
• To be self-motivated with ability to work on own initiative.
• Be willing travel to Cairn Sites Nationwide and hold a full driver's licence.
• Previous experience using mobile devices to capture, upload and report defects would be beneficial

Working with Cairn:

At Cairn, we believe it is essential that our employees feel valued and appreciated. We therefore offer above industry average remuneration packages with a comprehensive benefits portfolio that's ready to support you for whatever life brings.

We are delighted to offer a suite of benefits when you join Cairn which include;

• Competitive salary
• Performance related bonus
• Pension scheme with matching contributions
• Full health insurance with Irish Life health
• Annual salary review
• Continuous Professional development (CPD) programme & funding
• Paid maternity & paternity leave
• Free Cairn annual leave days
• Life assurance
• Income protection
• Employee Assistance Programme with VHI
• Tax saver - travel and bike to work
• Culture Committee
• Talent Development Programmes
• Approved Profit Sharing Scheme (APSS)
• Company vehicle (role dependent)

The Cairn purpose is to build sustainable communities where people can thrive.

At Cairn, it's not what we build, it's why we build. It's about putting down a marker that will stand for generations to come. Creating new communities of connection and belonging for an Ireland where people can thrive. Reshaping, redefining, reinvigorating our place in the world. Building for people, progress, and potential.

Because when Cairn build, it's Built For Good.

About Your New Employer

Join a
leading Irish food production company
known for its commitment to quality, safety, and innovation. The business has built a strong reputation for delivering consistent, high-quality food products across Ireland and international markets.

With a focus on teamwork, excellence, and continuous improvement, this company offers a supportive environment where your expertise and initiative will make a real impact.

About Your New Job

As the
Quality Assurance Specialist
, you will play a key role in ensuring the highest standards of food safety, quality, and compliance across production. You'll support and lead quality systems, internal audits, and technical standards, working closely with operations, innovation, and supply chain teams.

• Organising, training, and supporting the QA team to meet production and quality goals.
• Acting as a key advocate of food safety and compliance culture across the site.
• Maintaining, improving, and developing systems that support food safety programs.
• Ensuring compliance with Irish and EU regulations.
• Leading internal audits and assisting with corrective actions.
• Managing supplier quality and compliance with cross-functional teams.
• Implementing and maintaining technical standards and documentation.
• Acting as the technical lead during customer audits and site visits.
• Monitoring industry trends and regulatory updates to keep the business ahead of the curve.
• Exploring innovative approaches to drive continuous improvement and team motivation.

What Skills You Need

• Degree or qualification in a scientific or food-related discipline.
• 3+ years of experience in a similar QA or technical role.
• Experience in FMCG or food manufacturing, with team leadership exposure.
• Strong understanding of food processing and regulatory requirements.
• Working knowledge of IFS and Organic standards.
• HACCP certification with strong HACCP and auditing skills.
• Excellent communication, organisational, and problem-solving skills.

What's Next

If you're a proactive and detail-oriented professional looking to further your career in food quality assurance, we'd love to hear from you

Apply now or contact
Patricia
for a confidential discussion about this opportunity.

Hovione
is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated
Contract Development and Manufacturing Company
dedicated to helping
Pharmaceutical
Customers bring new and off-patent drugs to market.

Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites.

Working at Hovione means reaching for
innovation
and
excellence
in everything we do: for our clients, our partners and, above all, our patients.

That is why we are In it for life.

Responsibilities

Guarantees cGMP
compliance
in all activities and systems related to Projects and Products execution. Assures that working practices are streamlined and aligned with the actual needs of each project. Implements policies, procedures and methods to evaluate and to continuously improve the quality of products and operations throughout the products lifecycle.

Provides global supplier qualification services in support of new product introduction and existing products. Collaborates with suppliers and Procurement to assure the quality of their products, materials, components and/or operations.

• Rigorously, accurately, efficiently and professionally manage all quality activities for the assigned projects and / or products in accordance with applicable cGMP, quality operational standards / procedures and legal regulations, ensuring the site is always "audit ready"
• Promote the importance of high-quality levels and the importance of a continuous improvement culture in relevant company activities
• Act as a catalyst for change and improvement in performance/quality
• Provide an example of professionalism
• Assigned projects may relate to any of the following (non-exhaustive) areas: Raw Materials, Suppliers, Specifications, Production Processes, Change Control, Deviations, Quality agreements, Qualification and Validation, Stability Programs, Batch Release, Equipment Cleaning, Client Audits, Internal Audits, Customer Complaints, Customer requirements, PQR
• Efficiently, accurately and reliably ensure that project and / or product activities are delivered in compliance with cGMP requirements and maintenance of the company Quality Management System is assured
• Manage and participate in Quality Product key activities for the assigned product / projects, and introduction of new products; including (but not limited to) preparation, review and approval of auxiliary documentation, protocols and quality related reports
• Prepare for and support internal and external site audits and inspections, conducting regular reviews and periodically following-up action plans as necessary
• Ensure inspection readiness in work completed and Act in an advisory capacity for all internal and external site audits
• Periodic follow-up of ongoing deviations and Change Controls (PdAs) to assure timely closure of deviations and approval of PdAs, as appropriate
• Prepares SOPs, department
  IOPs
  , quality related reports and change control documents (PdAs) as required and appropriate
• Review process master
  documentation
  , revision of executed batch documentation and product specifications as required and appropriate
• Ensures that
  SOPs
  and IOPs are up to date, compliant and supports efficient production
• Review regulatory documentation and co-ordination of site documentation to support regulatory requirements
• Authorize the usage of production equipment/utilities when qualification required
• Solve challenges related to compliance problems by providing collaborative and timely support to all areas and departments, escalating as required
• Ensure the effective and proactive flow of information between stakeholders, representing the team as appropriate
• To assure and promote compliance on Health, Safety and Environment in the area and activities for which is responsible, or in which participates
• To maintain a regular presence on manufacturing floor, providing on-the-job support, developing a sense of collaboration with operational areas and performing a general oversight of activities, as required.
• Accurately use and maintain all information systems
• Support the generation / reporting of KPIs for the team
• Develop and accumulate strong QA expertise, sharing knowledge of new developments and methodologies within the area
• Co-ordinate and assist with the analysis and investigation of customer complaints that may arise, ensuring all complaints are investigated and closed out within specified timeframes
• Be an advocate for safe operating and high-quality performance, alerting ascending colleagues to any potential risks, discrepancies, deviations or non-conformance in accordance with Hovione internal procedures, suggesting optimizations or improvements, including those that have the potential to mitigate unnecessary complexity
• Apply and develop knowledge of Quality Assurance and participate in area processes, procedures and projects with the guidance of more senior colleagues
• Perform to ensure all assigned tasks are delivered on time, safely, efficiently, reliably and in a cost-effective manner
• Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others)
• Undertake any additional tasks commensurate with the role as and when required
• Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice.

Qualifications

• University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar scientific field (mandatory)
• Requires educational / training experience in a
  QA GMP
  environment within the
  Pharmaceutical
  Industry (desirable)
• Experience of working in a GMP operational environment (desirable)
• Training and experience of GMP standards (desirable)
• Experience of working with
  Regulatory Affairs
  and a basic knowledge of the function (desirable)
• Knowledge of
  GMP
  practices
• Fluency in
  English
  is a requirement
• Computer literate with good working knowledge of the MS Office package
• Good
  documentation
  skills and attention to detail
• Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down

Hovione is a proud Equal Opportunity Employer

Inclusion
and
diversity
are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

Your career at Deutsche Börse 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

Quality Assurance Specialist (Sterile / Aseptic experience essential)

Location: Little Island, Cork

Duration: 12 months

Hours: Full time, 39 hours per week

Imagine your next project as a
Quality Assurance Specialist
, working at the forefront of cutting edge work and technology with one of the leading Pharmaceutical companies in the world

roles and responsibilities

• Batch Record Review and material release (including CoA) to ensure compliance with GMP requirements.
• Quality review and approval of Master Batch Record (MBR) record for routine cleaning and process activities, including Automation recipe updates.
• QA Review and Approval of SOPs, Work Instructions and forms from other departments.
• Attendance at Daily/Weekly Operations led Team Meetings.
• Responsible for Gemba Walkdowns & Inspection
• Readiness Walkdowns from a QA perspective.
• QA review and approval of Warehouse Shipping Picklist.
• Primary QA point of contact for Quarantine Shipments.
• Responsible for Batch Book Filing & Archival.
• QA review and approval of quality non-conformance (NC) records and customer complaint non-conformance records.
• Initiation and ownership of QA non-conformance records.
• Confidential - FOIA Exemptions Apply in U.S.
• Responsible for periodic review of Quality Assurance and Quality Systems SOPs.
• Primary Quality point of contact for attendance at Root
• Cause Analysis meetings.
• Primary QA point of contact for the Returns process.
• Assisting with Audits

how to succeed

The successful candidate will be able to build strong relationships, have excellent communication skills, have the ability to work with teams and individuals. They will also bring:

• A minimum of 3 years of experience within the
  Pharmaceutical Industry
• ESSENTIAL - Requires strong experience and knowledge with sterile/aseptic environments
• Third level Degree in a science or pharmaceutical discipline.
• A working knowledge of quality processes and systems is desirable.
• Demonstrated knowledge and application of industry regulations including those of FDA, HPRA, EMEA and other authorities.
• Experience with preparing for Audits

benefits

This role offers a very competitive hourly rate. This contract will run for a
12 month duration.

you are welcome here

Johnson & Johnson Innovative Medicine
is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.

Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

Janssen Ireland:

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, LTD & Umbrella options are available.

questions

If you would like some additional information about the role please contact:

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means "You Belong".

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.

QUALITY MANAGER

MILLSTREET, CO. CORK | FULL-TIME | PERMANENT

THE ROLE

Office-based position with monthly site visits. Oversight of quality, health & safety, environmental standards.

KEY RESPONSIBILITIES

• Lead and oversee all aspects of quality management
• Ensure compliance with health, safety, and environmental regulations
• Conduct regular audits, inspections, and risk assessments
• Support continuous improvement across teams

QUALIFICATIONS

• Min. 10 years' experience
• University educated
• Pharma tech background preferable

WHAT WE OFFER

• €100k+ salary, depending on experience
• Package & benefits
• Strong on quality, health and safety, environmental

QA Resources is currently recruiting for a QA / Quality Specialist on behalf of a leading pharmaceutical company based in Cork. This is an initial 3-month project specific contract role.

Job Summary:

The QA / Quality Specialist will be part of a project team responsible for reviewing batch release documentation.

Responsibilities:

• Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records
• Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures

Education and Experience:

• Degree in Science, Quality, or a related Technical field.
• Experience in GMP Manufacturing or Quality Assurance environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing operations.
• Strong experience with documentation review
• Strong written and verbal communication skills

Interested candidates should submit an updated CV.

Please click the link below to apply, call Kellie on or alternatively send an up to date CV to

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

The role:

QA Resources is currently recruiting for a QA / Quality Specialist on behalf of a leading pharmaceutical company based in Cork. This is an initial 3-month project specific contract role.

Job Summary:

The QA / Quality Specialist will be part of a project team responsible for reviewing batch release documentation.

Responsibilities:

• Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records
• Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures

Education and Experience:

• Degree in Science, Quality, or a related Technical field.
• Experience in GMP Manufacturing or Quality Assurance environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing operations.
• Strong experience with documentation review
• Strong written and verbal communication skills

Interested candidates should submit an updated CV.

Please click the link below to apply, call Kellie on or alternatively send an up to date CV to

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***