What Quality Managers Jobs are in Ireland?

Showing 549 Quality Managers jobs in Ireland

Quality Systems & Compliance Manager

Posted today

Job Viewed

Tap Again To Close

Job Description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
**Position Summary**
The Manager, Quality Systems & Compliance is responsible for leading and continuously improving the site's Quality Systems and Compliance programme to ensure conformity with applicable regulatory, corporate, and site requirements. The role will drive a culture of quality and compliance across the organisation while supporting business objectives and minimizing operational disruptions.
The successful candidate will provide leadership for key Quality Management System (QMS) processes, oversee data integrity activities, support regulatory inspections and audits, and work cross-functionally to ensure the highest standards of product quality, compliance, and patient safety.
**What You'll Do**
**Quality Systems & Compliance Leadership**
+ Lead and manage the site Data Integrity Programme, including SOP governance, compliance assessments, risk management activities, and site-wide data integrity initiatives.
+ Support the implementation and continuous improvement of the Grifols Quality Systems & Compliance Programme.
+ Ensure compliance with corporate, regulatory, and site requirements.
+ Identify compliance risks and recommend improvements to quality systems and processes.
+ Quality Management System (QMS) Oversight
+ Manage and coordinate key Quality Systems including:Change Control, Deviations,Corrective and Preventive Actions (CAPA),Supplier Quality ManagementSupplier Complaints and Supplier Agreements, Documentation Control,Training Compliance, Quality SAP Processes, Other Quality System activities as required
**Compliance & Regulatory Support**
+ Support compliance activities across the site, including variation submissions, product specification compliance, new product introductions, and implementation of new manufacturing processes.
+ Support site readiness for regulatory inspections, customer audits, and corporate audits.
+ Coordinate and ensure timely completion of corrective actions arising from audits, inspections, and compliance assessments.
+ Participate in investigations of quality system issues and drive effective CAPA implementation.
**Documentation & Reporting:**
+ Manage the Documentation Compliance Management (DCM) system.
+ Oversee QMS document archives and records management activities.
+ Generate and communicate site Quality System metrics and compliance reports.
+ Support Site Quality Council activities and Annual Product Review processes.
+ Analyse and trend quality data to identify opportunities for continuous improvement.
+ Supplier & Audit Management
+ Support supplier qualification programmes and supplier quality activities.
+ Conduct or support supplier and outsourced provider audits as required.
+ Coordinate site self-inspection programmes and follow-up activities.
+ Support external audit preparation and facilitate audit activities.
+ Cross-Functional Leadership
+ Partner with Manufacturing, Engineering, Supply Chain, Quality Control, Regulatory Affairs, and other functional groups to resolve quality and compliance issues.
+ Communicate quality and compliance requirements across the site.
+ Identify and share best practices within the organisation and across Grifols manufacturing sites.
+ Deliver or coordinate GMP and quality system training where required.
+ Lead, coach, and develop Quality Systems & Compliance personnel.
+ Foster a culture of accountability, engagement, collaboration, and continuous improvement.
**What You'll Bring**
Education & Experience
+ Bachelor's degree in Science, Engineering, Pharmacy, Quality, or a related discipline.
+ Significant experience within a regulated pharmaceutical, biotechnology, medical device, or healthcare manufacturing environment.
+ Strong working knowledge of Quality Management Systems and GMP requirements.
+ Experience managing quality systems such as Change Control, Deviations, CAPA, Document Control, Training, and Supplier Quality.
+ Experience supporting regulatory inspections and audit programmes.
+ Previous leadership or people management experience is desirable.
+ Technical Skills Strong understanding of GMP, Quality Risk Management, and Data Integrity requirements.
+ Experience working with electronic Quality Management Systems and SAP.
+ Excellent analytical and problem-solving capabilities.
+ Strong project management and organisational skills.
+ Ability to manage multiple priorities simultaneously.
+ Excellent communication and stakeholder management skills.
**Our Benefits Include :**
+ Highly competitive salary
+ Annual performance-based bonus
+ Share options scheme
+ Group pension scheme with company matching contributions
+ Private Medical Insurance
+ Ongoing opportunities for career development
+ Succession planning and internal promotion opportunities
+ Education assistance
+ Wellness and social activities
+ Collaborative and inclusive working environment
We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply-we're excited to hear from you.
Location: Grange Castle International Business Park, Clondalkin, Dublin, Ireland.
**Location:** Grange Castle International Business Park, Clondalkin, Dublin, Ireland
Learn more about Grifols ( ID:**
**Type:** Regular Full-Time
**Job Category:**
Is this job a match or a miss?
Apply Now

Academic Quality and Compliance Manager

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description

Job description Who are we looking for? We are currently looking for an Academic Quality & Compliance Manager to join OnCampus Ireland, Maynooth. The role will be on a Part-time, Permanent basis. The Academic Quality & Compliance Manager is required to: Provide strategic academic quality leadership to the OnCampus Ireland Centre(s), to have overall responsibility for the academic standards of the Centres and is the designated person with responsibility for ensuring that the Centre(s) complies with relevant academic statutory, regulatory and accreditation agencies. Centre Director implements Quality Assurance policies and procedures including the management of academic staff, examinations and assessments, and the Academic Quality & Compliance Manager is responsible for active monitoring of these to ensure they are implemented to the required standards as set out by and agreed with regulators and awarding bodies. The Academic Quality & Compliance Manager is the main point of contact for QQI, IEM, ILEP and awarding bodies and reports to the CEO. Please note that interviews for shortlisted candidates and any potential job offers may be in place before the application end date. We recommend that, if interested in any of the roles, you apply as soon as possible. Required profile Education Masters qualified with a recognised TEFL certification (essential) Experience 5+ years of teaching experience in a QQI or equivalent accreditation environment, at least 2 of which are in an international or multicultural environment (essential) Experience designing curriculum (essential). 2+ years experience in managing programmes and centre management (essential). Extensive experience in a senior leadership role in an academic environment (essential). An understanding of Irish and EU higher education and the needs and requirements of international students (essential). Significant breadth and depth of English language teaching experience (Essential) Significant experience of devising and delivering high quality continuing professional development activities for teachers (Essential) Significant experience of conducting evaluation and review activities, building and implementing high quality SMART action plans leading to measurable improvement on delivery of services to students (Essential) Skills Demonstrates cross-cultural awareness and understanding (essential). A high degree of competence in the effective use of common Information Communications Technologies (ICT), particularly Microsoft Office packages and a variety for company IT systems and portals (essential) The ability to prioritise, meet deadlines and work under pressure (essential). What we offer Why will you love working here? Whether you work in one of our OnCampus or Managed Campus centres, in CEG Online supporting one of our many partner universities, or as part of one of our central service functions you will find a friendly, fast-paced and supportive work environment created by our diverse range of colleagues. Employee Values At Cambridge Education Group we believe that in living our values every single day we Achieve More for everyone around us, and in so doing makes it a great place to work. Expert Each individual strives to demonstrate expertise in everything they do, from previous experiences or acquiring new, relevant skills and know-how. We are great at sharing our knowledge to help our students, fellow colleagues and partners Achieve More. Authentic Our actions are taken, and decisions made, in line with our vision and mission; we trust everyone to do the right thing and deliver what they say they will through genuine, open and honest dialogue. We bring our whole selves to work, maximising our diversity to Achieve More. Innovative We continually improve all aspects of what we do, being solution-focused to affect change on our path to Achieve More. All colleagues share their ideas, big and small, and are flexible to new practices, approaches and ways of working. Whether you work in one of our OnCampus centres, with CEG Digital supporting one of our many partner universities, withIheed transcending boundaries, transforming medical education, in market engaging prospective students or as part of one of our central service functions you will find a friendly, fast-paced and supportive work environment created by our diverse range of colleagues. Benefits Perkbox (includes hundreds of discounts on brands) Employee Assistance Program (EAP) giving caring and compassionate support to all staff, as well as a dedicated Mental Health Support Network. Private Medical Staff Discount on CEG Digital courses Mentoring scheme Enhanced annual leave entitlement CEG is committed to safeguarding and promoting the welfare of children and vulnerable adults and expects all colleagues to share this commitment. All successful candidates will undergo background checks in the required countries. Where roles have direct contact with children, including all OnCampus centre- based roles, this will include ID, qualification and reference checks, criminal record checks including an Enhanced Disclosure (or equivalent) in line with safeguarding requirements and our Safeguarding and Prevent Policy (including Children Protection). Any offer of employment is subject to all checks being satisfactory. The Company also expects all colleagues to share the Companys commitment to Equal Opportunities within the workplace. Skills: academic compliance quality TPBN1_IJ

Is this job a match or a miss?
Apply Now

Supplier & TPM Quality Manager

Kilkenny Tirlan

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description

Company description: TIRLN LIMITED Job description: Supplier & TPMQuality Manager Abbey Quarter, Kilkenny, Co. Kilkenny Tirln Tirln, is a world-class food and nutrition co-operative, with a diverse portfolio of quality ingredients, leading consumer and agri brands. Tirln owns leading brands such as Avonmore, Kilmeaden Cheese, Millac, Solmiko, Truly Grass Fed, Premier Milk, Wexford, and GAIN Animal Nutrition. A talented team across Ireland, the US, MEA and China, delivers annual revenues of over €3 billion. Our purpose is to nourish the world, while safeguarding our environment for future generations. Overview The role will aid the design and delivery a quality oversight model for all third-party activities in conjunction with others within the Q&C function and wider procurement and TPM team. The role will assist in the measurement, qualification and setting of specific goals & improvement plans for each supplier / third party manufacturer. Reporting to the Senior Supplier & TPM Quality Manager the successful candidate will ensure that the quality of the materials purchased & products manufactured on behalf of Tirln meet the legislative and regulatory standards as well as our internal customers in the case of suppliers and customer expectations for the out sourced products in question. Key Responsibilities Qualify & approve suppliers/third party manufacturers (TPMs) prior to use in accordance with Tirln food safety & quality requirements and GFSI requirements Assess compliance of systems, facilities, and procedures per applicable regulations through documentation review, food safety assessments & on-site audit. Assuring compliance to regulatory requirements and company specifications; Provide feedback in the form of audit observations; review corrective actions to confirm actions and commitments have been properly implemented, proven to be effective and are being maintained at the supplier service level; Plan & execute risk-based supplier assessments and audit programmes through Safefood 360 our Supplier Management Platform Contribute on behalf of quality operations & systems for innovation projects developed with TPMs. Participate in new product launches; Act as Tirln quality contact with retailers where applicable for products which are supplied via a TPM; Maintain all quality related documentation in a structured & organized fashion that is available to the business; Sign off on agreed specification from a quality perspective and quality SLA for end product/service where applicable; Support/prepare the collection and consolidation of data for quality KPIs to monitor the capability and performance of suppliers; Prepare the data for supplier / TPM Performance management reviews; Work with each business to identify and tracks quality issues: addresses non-conformances with third parties through Tirln RCA equivalent process; Participate in strategic initiatives to improve compliance to regulatory requirements and standards; Escalate issues to management that involve food safety, warranty risk, liability & or cost. Prioritize actions based on risks, faults & impact; Complaint management including the engagement with suppliers/third parties to agree CAPA & close out; Oversight of key third party product manufacture including site visits and product inspection; TPM product release; review batch records and COA; release of product batches; Completion of customer requests as required by the business; Any ad hoc activities as specified by the reporting manager. Key Requirements: Minimum bachelors degree in science or related discipline; Extensive experience in food, feed or dairy industries; Demonstrated expertise in GFSI-recognised standards (e.g. BRCGS, FSSC 22000) and retailer requirements Proven track record in supplier quality management and auditing, with a lead auditor qualification an advantage Strong understanding of food safety risk management frameworks and EU regulatory requirements, in relation to both food and feed products; Team player with focus on improvement and a strong drive for results. Competencies Analytical, organisational & Problem solving skills Excellent interpersonal & communication skills; Attention to detail; Organisational agility; Ability to plan, multitask and understand departmental priorities; Driving licence. We offer Hybrid working (flex Fridays) Free parking Work/life balance and collaborative work culture Career progression opportunities About us Through our expertise in research and development, customer insights, food safetyand state-of-the-art manufacturing we bring innovative food and nutrition solutions to a global market. Our new and vibrant headquarters in Kilkenny City operates as a collaboration hub where multi-functional teams come together in a hybrid work environment. Commitment to Diversity & Inclusion We believe in the value of difference. We know that different perspectives, life experience and backgrounds can drive innovation and deliver growth. We welcome people from all walks of life without regard to race, colour, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, or disability status. Join our Talent Pool Considering a new career in Tirln but this isnt the role for you? Join our talent community and sign up for job /careers Tirln is a Values Based Organisation Profile description: The role will aid the design and delivery a quality oversight model for all third-party activities in conjunction with others within the Q&C function and wider procurement and TPM team. The role will assist in the measurement, qualification and setting of specific goals & improvement plans for each supplier / third party manufacturer. Reporting to the Senior Supplier & TPM Quality Manager the successful candidate will ensure that the quality of the materials purchased & products manufactured on behalf of Tirln meet the legislative and regulatory standards as well as our internal customers in the case of suppliers and customer expectations for the out sourced products in question. Skills: Supplier Quality Management Food Safety & Regulatory Compliance Quality Auditing & CAPA Benefits: Paid Holidays Parking Pension TPBN1_IJ

Is this job a match or a miss?
Apply Now

Quality Manager

Clonmel Abbott

Posted 1 day ago

Job Viewed

Tap Again To Close

Job Description

**Main Purpose of the Role**
Provide management of a functional area that results in the implementation and achievement of vision, mission and functional objectives. This position is responsible for overseeing and directing Quality Engineering, Supplier Quality Engineering, Regulatory Compliance, Analytical laboratories, Product release and Quality Control functions, as required, to support Manufacturing, Supplier Development, New Product Development and Quality Systems.
Plans, develops and manages the quality organisation to assure the continuance of qualified and efficient staff to meet Corporate, Food and Drug Administration (FDA), International Organisation for Standardisation (ISO) requirements as well as other regulatory requirements as captured in COP381.
Ensures the overall compliance and effectiveness of the quality system with established requirements and quality system regulations.
Directs projects to ensure the manufacture of high quality product and to facilitate compliance with requirements.
Evaluates performance of direct reports and supports career development activities. Ensures that program and project objectives are met, budgets are adhered to and metrics are captured and published.
**Main Responsibilities**
+ Recruits, coaches and develops organisational talent.
+ Fosters a diverse workplace that enables all employees to contribute to their full potential in pursuit of organisational objectives.
+ Creates an entrepreneurial environment that encourages innovation and accountability.
+ Provides direction and guidance to exempt specialists and/or supervisory staff who exercise significant latitude and independence in their assignments; may supervise non-exempt employees.
+ Keeps the organisation's vision and values at the forefront of decision-making and actions.
+ Demonstrates effective change leadership.
+ Builds strategic partnerships to further departmental and organisational objectives.
+ Develops and executes organisational and operational policies through the application of technical and professional expertise.
+ Monitors compliance with company policies, FDA, BSI and other applicable regulatory requirements.
+ Makes decisions regarding work processes, operational plans and schedules to achieve department and site objectives.
+ Develops, monitors and manages the annual budget for areas of responsibility.
+ Approves documents defining the quality system.
+ Reviews subcontractors', suppliers' and service providers' quality systems to ensure purchased products fully comply with specified requirements.
+ Participates with manufacturing management at all levels in resolving quality and reliability issues.
+ Ensures valid test data is used for all regulatory submissions.
+ Oversees completion of the Annual Product Review process as required.
**Minimum Requirements**
+ Bachelor's degree (NFQ Level 7 or equivalent) in a relevant scientific, engineering, quality or related discipline.
+ Minimum 9 years' experience in a regulated laboratory, pharmaceutical, medical device or quality environment.
+ Proven people leadership experience with responsibility for coaching, developing and managing technical teams.
+ Strong knowledge of quality systems, regulatory compliance and laboratory operations.
+ Experience supporting regulatory submissions and ensuring the integrity of analytical test data.
+ Demonstrated experience managing audits, supplier quality activities and quality improvement initiatives.
+ Strong stakeholder management skills with the ability to collaborate effectively across Manufacturing, Quality and Regulatory functions.
+ Experience managing departmental budgets, operational plans and strategic objectives.
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
Is this job a match or a miss?
Apply Now

Quality Manager

Posted 1 day ago

Job Viewed

Tap Again To Close

Job Description

Quality Manager/Regional Director Nursing Home Group Location: Midlands preferred; however, applications from candidates based elsewhere in Ireland will be considered. Regular travel to nursing homes across Ireland is required. Advent Solutions is seeking an experienced and driven Quality Manager/Regional Director to oversee the operations of a portfolio of nursing homes across Ireland. Reporting directly to the CEO, this senior leadership role is pivotal in ensuring excellence in resident care, regulatory compliance, operational performance and the ongoing development of high-performing clinical teams. Key Responsibilities Lead the day-to-day operational management and governance of nursing homes within your region. Ensure full compliance with all regulatory, clinical governance and quality standards, including effective risk management. Develop, implement and monitor operational policies, procedures and best practices. Drive continuous improvement in the quality of care, resident experience and service delivery. Partner with Directors of Nursing to develop and implement quality improvement initiatives and action plans. Support the delivery of the Group's strategic and operational objectives. Monitor and achieve financial and operational KPIs across your region. Provide leadership, coaching and support to Directors of Nursing and their management teams. Oversee workforce planning, recruitment, retention and staff development initiatives. Build strong relationships with internal and external stakeholders while promoting a culture of excellence, accountability and continuous improvement. Requirements Registered General Nurse with current registration with the Nursing and Midwifery Board of Ireland (NMBI). A minimum of 10 years' post-registration experience, including at least 3 years within the previous 6 years in the care of older persons. At least 2 years' senior leadership experience as a Director of Nursing or above within the nursing home sector. Post-registration qualification in Healthcare Management, Leadership or a related discipline. Excellent knowledge of the Health Act 2007, HIQA standards and clinical governance. Proven ability to lead multiple services, manage change and deliver strategic objectives. Strong commercial awareness with experience managing budgets and operational performance. Full clean driving licence and willingness to travel nationwide. Compensation & Benefits Competitive salary depending on experience. Performance-related bonus. Opportunity to join a progressive organisation with genuine scope to influence quality, operational excellence and future growth. To arrange a confidential discussion or to apply, send your CV to Alan Noone at Advent Solutions for an initial consultation.
Is this job a match or a miss?
Apply Now

Quality Manager

Posted 1 day ago

Job Viewed

Tap Again To Close

Job Description

Job title: Quality Manager Location: Galway Benefits: Top salary, Bonus, pension, healthcare and hybrid. Company: My client are a Medical device manufacturer with a new hub in Galway. They specialise in catheters, medical balloons, EM-Micro Sensors, engineered shafts, and complete device assemblies, supporting a wide range of interventional therapies. Responsibilities: Act as the Management Representative for the Quality Management System (QMS). Ensure the QMS processes and documentation are established, implemented, and maintained in compliance with ISO 13485, ISO 9001, and 21 CFR Part 820. Report on QMS performance and identify opportunities for continuous improvement. Promote awareness of regulatory and customer requirements across the organization and ensure compliance. Serve as the primary liaison with customers and certification bodies for external audits. Provide leadership and direction on all QA-related matters, including quality systems, compliance, and material disposition. Ensure management review meetings are conducted in accordance with regulatory requirements. Oversee control of documents and records related to products, manufacturing processes, and the QMS. Plan, manage, and conduct internal quality audits to ensure compliance with applicable standards and internal procedures. Handle and monitor CAPA, customer complaints, and feedback to ensure timely resolution and continuous improvement. Carry out supervisory responsibilities in accordance with company policies and applicable laws, including interviewing, hiring, training, performance management, and employee development. Plan, assign, and direct work; evaluate performance; recognize achievements; address employee concerns. Requirements: Education/Experience and Qualifications: 510 years of progressive experience in quality assurance and control within medical device manufacturing or a related industry, with in-depth knowledge of manufacturing processes and quality systems. Strong management and leadership skills. Solid knowledge of ISO 13485, FDA 21 CFR Part 820, and/or Medical Device Directives. Demonstrated proficiency in engineering and quality tools (e.g., FMEA, DOE, SPC, and statistical analysis tools). Ability to support product development, manufacturing, and product release activities as directed by senior management Does this sound like your next career move? To apply and for more info forward your application to the link provided or contact me on OR Benefits: Bonus, pension, healthcare, hybrid
Is this job a match or a miss?
Apply Now

Quality Manager

Posted 1 day ago

Job Viewed

Tap Again To Close

Job Description

My client is a leading Civil Engineering contractor with a strong reputation for delivering high-quality large-scale residential and commercial projects across Dublin. With a robust project pipeline and continued growth, they are seeking an experienced Quality Manager to drive excellence and maintain industry-leading standards across all sites. The Quality Manager will take responsibility for developing, implementing, and maintaining the companys Quality Management System (QMS) in line with regulatory and client requirements. This role will ensure that all works are delivered to the highest quality standards across multiple concurrent projects. Duties: Lead the implementation and continuous improvement of the Quality Management System (QMS) in line with ISO 9001 standards Develop and manage inspection and test plans (ITPs) and quality assurance procedures Conduct regular site audits, inspections, and compliance reviews across multiple projects Work closely with project managers, engineers, and site teams to ensure quality standards are embedded from planning through to completion Identify, investigate, and resolve non-conformances, implementing corrective and preventive actions Maintain accurate and up-to-date quality documentation and reporting systems Liaise with clients, consultants, and regulatory bodies regarding quality standards and compliance Deliver training and guidance to site teams to promote a culture of quality and continuous improvement Support project teams in meeting handover and certification requirements Monitor subcontractor performance to ensure adherence to quality standards Requirements: Degree-qualified in Civil Engineering, Construction Management, or a related discipline Minimum 5+ years experience in a quality-focused role within civil engineering or construction Strong knowledge of ISO 9001 Quality Management Systems Proven experience working on large-scale residential and/or commercial projects Excellent understanding of construction processes, materials, and industry standards Strong analytical and problem-solving skills with a proactive approach Excellent communication and stakeholder management abilities Ability to manage multiple projects simultaneously Whats on Offer: Salary circa €70k - €80k DOE Vehicle Opportunity to work with a market-leading contractor on high-profile projects Strong pipeline of long-term work in Dublin Career progression opportunities within a growing organisation Collaborative, high-performance working environment If you are aQuality Managerconsidering a career move, please feel free to send yourCV or contact Lisa Cullen on for a confidential discussion.GPC will not send any applicants CVs to clients without a full discussion and prior consent. GPC is a specialist construction recruitment consultancy based in Dublin with 24 years experience working in the recruitment of construction professionals within Ireland and Internationally. Skills: Quality Manager
Is this job a match or a miss?
Apply Now

Quality Manager

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description

Quality Manager | Medical Devices | Co. Offaly | Onsite role We're partnering with a leading manufacturer in the regulated healthcare sector to recruit an experienced Quality Manager. This is an excellent opportunity to join a high-performing leadership team and take ownership of the site's Quality Management System while driving compliance, continuous improvement, and operational excellence. Key Responsibilities Lead, coach and develop the Quality team, fostering a high-performance, quality-first culture. Own and continuously improve the site's Quality Management System (QMS), ensuring compliance with relevant regulatory and industry standards. Lead Management Review activities, including planning, reporting and follow-up actions. Manage customer complaints, CAPA, document control, change control and internal audit processes. Coordinate and lead customer, certification and regulatory audits, ensuring successful outcomes. Monitor quality metrics and KPIs, providing meaningful analysis to support business decision-making. Drive continuous improvement initiatives using Lean, Six Sigma or similar methodologies. Partner with cross-functional teams to identify risks, resolve quality issues and improve manufacturing processes. Provide leadership on product quality, non-conformance investigations and material disposition. Support standardisation and best practice initiatives across multiple manufacturing sites where applicable. Ensure all Quality activities are carried out in line with Environmental, Health & Safety requirements. Background: Degree in Engineering, Science or a related technical discipline (Master's degree advantageous). 5-8 years' experience within Quality Engineering or Quality Management in medical devices or another regulated manufacturing environment such as pharmaceuticals, biotechnology, aerospace or defence. Previous experience leading Quality teams within a manufacturing environment. Strong knowledge of Quality Management Systems and regulatory requirements, including ISO 13485, FDA Quality System Regulations and risk management principles. Experience managing internal and external audits, CAPA, complaints, change control and document control systems. Certified Quality Auditor (ASQ or equivalent) is desirable. Experience applying Continuous Improvement methodologies such as Six Sigma or Lean. Strong analytical, project management and problem-solving skills. Excellent communication and stakeholder management abilities, with confidence influencing teams at all levels. High level of proficiency in Microsoft Office applications. A more detailed job description is available upon request. TPBN1_IJ

Is this job a match or a miss?
Apply Now

Quality Manager

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description

West Cork | Full-time | Permanent Join a well-established, growing food producer with a strong team culture and genuine family feel. We're looking for an Assistant Quality Manager to support day-to-day quality operations and step up when needed. This is a hands-on role with real responsibility and clear progression. The Role Lead the Quality function in the Manager's absence Run internal, customer, and regulatory audits Maintain HACCP, Quality Systems, and Food Safety standards Ensure full compliance with FSAI and industry requirements Act as key contact for suppliers and customers on quality matters Drive food safety, quality, and corrective actions on the floor Support and guide the Quality team Monitor standards, report issues, and improve processes About You Food Science (or related) qualification Experience in food manufacturing quality Strong HACCP and audit knowledge Confident, proactive, and able to lead when required Why Apply Great company with a supportive, down-to-earth culture Strong team environment Real opportunity to grow your career Apply now for a confidential discussion. Consultant: Mandy Devlin Please note, you need to be in Ireland and eligible to work in Ireland to apply for this job. You may have searched for QM job Cork, Cork QM jobs, Cork quality manager job, Cork assistant quality manager job, assistant quality manager job cork, Irish jobs quality manager food Cork Skills: quality manager food TPBN1_IJ

Is this job a match or a miss?
Apply Now

Quality Manager

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description

Cork | Permanent | Manufacturing Our client, a well-established and highly respected manufacturing organisation based in Cork, is seeking an experienced Quality Manager to join their leadership team. Reporting to the Managing Director, you will lead the Quality function, ensuring products consistently meet customer specifications and recognised industry standards while driving continuous improvement across the business. Key Responsibilities Lead and develop the company's Quality Control systems and procedures. Manage and maintain the ISO 9001 Quality Management System. Ensure products meet customer requirements and relevant quality standards. Lead internal and external quality audits. Manage customer complaints and oversee CAPA investigations and implementation. Monitor quality performance, analyse data and produce management reports. Lead, mentor and develop the Quality team. Collaborate with production and management teams to drive continuous improvement initiatives. Promote a strong culture of quality, compliance and safety. About You Degree in Engineering, Quality Assurance or a related discipline. Minimum of 5 years' experience in a Quality Management role within a manufacturing environment. Strong working knowledge of ISO 9001 Quality Management Systems. Experience leading audits, managing CAPAs and implementing quality improvements. Excellent leadership, communication and problem-solving skills. Strong analytical ability with experience producing quality reports. Lean Manufacturing and/or Lean Six Sigma experience is advantageous. If you would like to find out more about this role please click the 'Apply Now' button below or reach out to Kellie on Skills: Quality Management ISO 9001 Leadership CI Process improvement Audit management TPBN1_IJ

Is this job a match or a miss?
Apply Now