207 Senior Quality jobs in Ireland
Quality Manager

Posted 27 days ago
Job Viewed
Job Description
Reports to: Regional/Cluster Quality Manager
Job Purpose
The role focuses on compliance, customers, and continuous improvement activities to create a total quality culture and reduce quality costs in line with best practice procedures.
u2022 To protect and please the customer by ensuring supply of the highest quality product
u2022 Working with production and support functions to maintain and improve our quality systems and adherence to operational best practice thus guaranteeing compliance to external and internal standards
u2022 To drive improvement activities to support quality and financial performance leading key improvement projects evolving through customer requirements, legislative changes, and amendments to accredited standards to ensure compliance with standards and pending accreditation audits
u2022 Draft, review and implement changes to our current quality systems, standard operating procedures, and policies to satisfy customer and third-party requirements
Role Responsibilities
Key Responsibilities - Quality
u2022 Support the Cluster Manager and site Leadership team in quality governance
u2022 Lead and support meetings as required and provide information and analysis as required to support the business in understanding KPIu2019s and decision making
u2022 Review the quality system as appropriate to ensure full compliance with customer and company best practice guidelines and maximize effectiveness of production contributing to consistent operational performance and standards whilst ensuring conformance to the relevant accreditation standards for the site and customers
u2022 Provide authoritative guidance and advice on all aspects of quality to the site management team and employees; train and coach employees improving knowledge and skills in quality improvement
u2022 Recruit, develop, motivate, and manage a Quality team (QA/QC) that optimises quality operations and is flexible in the support it offers the business, meeting current and future needs
u2022 Establish and develop professional working relationships with customers, providing a technical service and reference point as required to support the companyu2019s products and reputation as a quality supplier
u2022 Manage the customer complaint procedure, facilitate the investigation of quality problems, faults, and non-conformances with production teams; manage corrective and preventative problems to ensure quality standards are maintained. Initiate and control robust investigations to provide corrective and preventive actions (CAPA) and support the complaints handling process and participate in implementing improvement actions to prevent re-occurring issues.
u2022 The facilitation of customer facing activities and communications including customer visits, responses, and preparation of information whilst leading site audit activities (external body, internal and customer)
u2022 Lead quality initiatives and focus groups to support knowledge and understanding of all operatives and grow awareness of quality issues to improve quality
u2022 Promote a total quality philosophy at all levels developing a culture of right first time and continuous improvement
u2022 Develop an Integrated Quality Management System including quality, environment and health and safety
Key Responsibilities - Business Improvement
u2022 Lead improvements to enhance quality system and ensure optimum process in place to meet customer specifications whilst maximizing production
u2022 Review amendments to standards and ensure compliance with accreditation bodies
u2022 Support introduction of new equipment on site and validation processes to meet safety and customer expectations
u2022 Take on other projects and responsibilities as required.
u2022 Contribute ideas and participate in ongoing business improvement initiatives to reduce overall operating costs, improve margin, and provide input into the strategy and operations of the site
Knowledge, Skills, Experience
u2022 Minimum 5 yearsu2019 experience in a Quality role at a senior or management level
u2022 Working and audit knowledge relevant accredited standards
u2022 Experience in a manufacturing/production environment ideally with experience and knowledge of Industry standards and guidelines
u2022 Demonstrable experience of leading change and implementing continuous improvement processes.
u2022 Supervisory experience
u2022 Demonstrable experience of validating new equipment and processes
u2022 Knowledge of Good Manufacturing Practices (GMP)
u2022 Project management and problem-solving skills such as 6 Sigma, or another recognised Business Improvement Technique
u2022 Root cause analysis and problem-solving techniques
u2022 Customer relations skills
u2022 Skilled in information handling, analysis, and presentation
u2022 Competent in using Microsoft Office packages
Smurfit Westrock (NYSE:SW) is a global leader in sustainable paper and packaging solutions. We are materials scientists, packaging designers, mechanical engineers and manufacturing experts with a shared purpose: Innovate Boldly. Package Sustainably. Guided by our values of safety, loyalty, integrity, and respect, we use leading science and technology to move fiber-based packaging forward.
Smurfit Westrock is an Equal Opportunity Employer. We strive to create and maintain a diverse workforce where everyone feels valued, respected, and included. Smurfit Westrock does not discriminate on the basis of race, color, religion, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other basis protected by federal, state or local law.
Quality Manager

Posted 27 days ago
Job Viewed
Job Description
Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
+ **Career Development** : Opportunities to grow and achieve your career aspirations within an international company.
+ **Benefits Package** : Excellent pension and family healthcare benefits.
+ **Recognition** : The company is recognized globally as a great place to work and has been named one of the most admired companies by Fortune.
+ **Diversity and Inclusion** : Known for being one of the best big companies to work for, especially for diversity, working mothers, female executives, and scientists.
**Responsibilities Include:**
+ **Establish and Maintain Quality Standards** Implement and uphold rigorous quality standards, ensuring compliance is consistently achieved throughout all phases of the process.
+ **Develop Quality Assurance Frameworks** Design and execute comprehensive quality assurance strategies in alignment with applicable regulations and industry best practices.
+ **Conduct Risk Assessments and Provide Guidance** Evaluate potential risks, ensure adherence to compliance requirements, and offer informed recommendations to mitigate issues effectively.
+ **Oversee Quality Control Activities** Assume full responsibility for quality control across all operational areas, including laboratory studies, clinical research, testing procedures, raw material sourcing, production processes, and final product or service delivery.
+ **Facilitate Audits and Inspections** Coordinate and support internal and external audits, as well as regulatory inspections, ensuring preparedness and compliance with relevant standards.
+ **Manage External Partnerships** Engage with vendors, contractors, and suppliers to verify that their products and services meet the organization's established quality criteria.
+ **Organize and Deliver Quality Training** Plan and conduct training programs to enhance quality awareness and ensure consistent application of quality standards across teams.
**Education and Years Experience:**
+ Minimum Level 7 National Framework Qualification or equivalent. Engineering/ Science disciplines preferred
+ Minimum 7 years' experience in manufacturing environment including 3 at leadership level
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.
Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Quality Manager
Posted 1 day ago
Job Viewed
Job Description
Quality Manager
Posted today
Job Viewed
Job Description
Quality Manager
Posted today
Job Viewed
Job Description
Quality Manager
Posted today
Job Viewed
Job Description
Quality Manager
Posted today
Job Viewed
Job Description
Be The First To Know
About the latest Senior quality Jobs in Ireland !
Quality Manager
Posted 27 days ago
Job Viewed
Job Description
Our client, an innovative and fast-growing medical device company based in Galway, is seeking a Quality Manager to join their expanding team. The company is currently transitioning from development to commercialization and is focused on delivering meaningful, patient-centered solutions in a dynamic and highly regulated environment. This is an exciting opportunity for a quality professional who thrives in a collaborative start-up culture. The successful candidate will play a key role in leading the quality function and shaping the company’s quality systems and compliance strategy as it moves toward global product launch.
Responsibilities include but are not limited to the following:
Lead and maintain the company’s Quality Management System (QMS), ensuring compliance with ISO 13485, QMSR, and other applicable regulatory standards.
Drive Management Review activities, track Quality Objectives, and monitor relevant KPIs.
Prepare and manage internal/external audits and regulatory reporting requirements.
Lead design assurance activities including design controls, verification and validation, and maintenance of the Design History File (DHF).
Develop and validate test methods to assess product performance and ensure compliance.
Oversee and maintain the Document Control System (QT9 eQMS), including administrative tasks.
Lead computer system validation/assurance efforts in line with regulatory requirements.
Manage CAPA, non-conformance investigations, and customer complaint processes.
Direct risk management and usability engineering activities, including user feedback and human factors inputs.
Support the Device Master Record (DMR) and Device History Record (DHR) documentation and control.
Lead Supplier Quality Management: qualification, audits, vendor reviews, and Approved Vendor List maintenance.
Support regulatory strategy, including GAP assessments and updates related to relevant standards.
Collaborate cross-functionally with R&D, Manufacturing, and Regulatory teams to drive continuous improvement.
Contribute to resource planning, team training, and performance management within the quality function.
Lead or support lot release and quality oversight in partnership with contract manufacturers.
Champion a culture of quality throughout the organization and act as a key stakeholder in preparing for market readiness.
Bachelor’s degree in engineering, science, or a related discipline (or equivalent experience).
Minimum of 5 years’ experience in a medical device environment, preferably in a start-up or early-stage company.
Strong knowledge of ISO 13485, GMP, FDA QMSR, and international regulatory requirements.
Hands-on experience with design assurance, quality systems, and supplier quality management.
Familiarity with ISO 14971 and risk management practices.
Experience with validation of test methods, sterilization (EtO or Gamma), packaging, biocompatibility, and labelling is a plus.
Demonstrated ability to lead audits, CAPA processes, and quality planning.
Strong analytical, problem-solving, and root cause analysis skills (DMAIC preferred).
Proficiency with MS Office and electronic QMS tools (e.g., QT9).
Excellent communication, leadership, and cross-functional collaboration skills.
Comfortable in a fast-paced, evolving environment with a hands-on, proactive approach
Immediate interviews available for suitable candidates.
Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other future vacancies.
Pale Blue Dot® Recruitment
The Experts in STEM Workforce Solutions
Associate Quality Manager
Posted 3 days ago
Job Viewed
Job Description
Working within a fast-paced environment the job holder will work with the Quality Manager providing support to the Quality department on day-to-day tasks. Working with the Quality Manager, the job holder will actively investigate and resolve customer quality queries, facilitate the success of continuous improvement teams, as well as identify any trends in quality issues before they become a problem.
Role Responsibilities
* Creating and updating various reports as requested by Quality Manager
* Managing the Internal and External OFI
* Support Quality Manage in leading and hosting BSI and Customer audits
* Working with the Management Team and Operations Teams to setup continuous improvement actions
* Progress chasing - CAPAu2019s, OFIu2019s
* Management of the internal audit system
* Provide support and manage as appropriate calibration system
* Manage the Supplier complaint system in Q-Pulse, provide metrics as required
* Investigation of customer daily queries
* Make informed decisions on quality in absence of Quality Manager
* Actively attend Site Quality Meetings - produce minutes
* Facilitate Continuous Improvement Teams - Including RCA tools
* Support QM in managing the internal CAPA system
* Manage and log annual leave and hours worked for QC team as requested by QM
* Develop Leadership style through the support and mentoring of Quality Manager
Quality System
* All functions to be carried out in accordance with ISO 9001:2015 quality management standard requirements with reference to the sites Quality Policy, Policy Manual & relevant Works Instructions.
* Work with Quality Manager to ensure that all aspects of PS9000 are integrated into the Quality system.
Knowledge, Skills, Experience
* Minimum 2 yearsu2019 experience in a Quality role at a senior supervisor or entry management level
* Working and some knowledge of the relevant accredited standards (not essential)
* Experience in a manufacturing/production environment ideally with experience and knowledge of Industry standards and guidelines
* Demonstrable experience of change management
* Supervisory experience
* Knowledge of Good Manufacturing Practices (GMP)
* Root cause analysis and problem-solving techniques
* Customer relations skills
* Skilled in information handling, analysis, and presentation
* Competent in using Microsoft Office packages
Other Requirements
Flexible and adaptable to change and prepared to take on additional responsibilities with other duties as required to meet business needs. Successfully adapts to changing demands and conditions. Be able to be self-motivated, standards driven, with a keen eye for detail whilst being team focused and harnessing collaboration and co-operation of others.
Smurfit Westrock (NYSE:SW) is a global leader in sustainable paper and packaging solutions. We are materials scientists, packaging designers, mechanical engineers and manufacturing experts with a shared purpose: Innovate Boldly. Package Sustainably. Guided by our values of safety, loyalty, integrity, and respect, we use leading science and technology to move fiber-based packaging forward.
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.
Group Quality Manager
Posted today
Job Viewed