What Quality Manager Jobs are in Ireland?
Showing 684 Quality Manager jobs in Ireland
Job Description
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
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Job Description
Is this job a match or a miss?
Job Description
Is this job a match or a miss?
Job Description
Is this job a match or a miss?
Job Description
Is this job a match or a miss?
Job Description
Job Title Quality Manager Job Location Co. Cavan Salary €50K - €65K Based on Experience About the Company: This is a standalone Quality Manager role and is designed to focus on the companys internal Quality development, driving quality and process improvements. You will bridge the gap between management, operations, suppliers, and end-users to ensure all outputs are fit for purpose, safe, and legally compliant. The quality manager focuses on all aspects that may affect product quality including materials, design, process, instruction, training and equipment. The quality manager achieves results through the Quality Process Engineers and Technicians. Duties Include: Plan and execute internal and external audits. Ensure all processes strictly meet national, international, and health/safety legal obligations. Looking after and developing ISO 9001/ FSC and potentially 45001. Assess supplier capabilities, conduct vendor audits, and manage corrective/preventative action (CAPA) processes when raw materials or parts fail to meet specifications. Establish product specifications, define testing methods, and enforce strict pass/fail standards for final products before they reach the market. Gather performance data, perform statistical analysis, and produce clear KPIs and reports for senior management. Lead root-cause investigations into customer complaints, product defects, or process bottlenecks to prevent them from recurring. Strong communication and influencing skills are critical. Because this is a standalone role, you must be able to drive change and motivate colleagues who do not directly report to you. Essential Criteria: Bachelors Degree Quality Management or Engineering. Expertise in regulatory compliance, Root Cause Analysis (RCA), and continuous improvement methodologies (e.g., Six Sigma, Lean). Typically, 5+ years in a Quality Assurance or Technical role, with proven experience operating autonomously or leading quality standards. Preferably 2-3 years in a people management role. In depth working knowledge of root cause analysis and problem-solving tools. Certifications such as ISO 9001:2015 Lead Auditor or a CQI membership are highly desirable. Proven record of delivering results through collaborative process improvements. Demonstrates full flexibility to undertake occasional travel to customer locations. If you feel this is an opportunity that interests you, please contact Caoln for more information on . INFORM3 Recruitment is an equal opportunities employer. By applying to this position, you accept the terms of our privacy policy, please find this on our website. Skills: Engineering Quality Management Quality Manager Regulatory Compliance Continuous Improvement Vendor Audits Quality Assurance TPBN1_IJ
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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
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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
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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
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Quality Manager Location Flexible Our client, a large nursing home group with homes nationally, is seeking applications for the role of Quality Manager. Location is flexible and the portfolio will be built around the candidates geographical location. The successful candidate will be joining an existing team which is expanding due to increased demand for quality service. You will lead quality and governance initiatives across multiple nursing homes, ensure compliance with HIQA regulations, conduct audits, develop improvement plans and mentor staff, oversee policy implementation and support staff training and promote a culture of continuous improvement and person-centered care To be considered for the role, the following criteria will apply: Registered Nurse (NMBI) with a postgraduate qualification in healthcare management, quality improvement or clinical governance 35 years experience in quality, governance, or compliance within healthcare Strong knowledge of HIQA standards and regulatory requirements Excellent leadership, communication and analytical skills Full Irish drivers license and willingness to travel If you are ready to lead quality in care and would like to discuss the role further, please contact Catherine Hoban on: T: E: #LI-CH5 Skills: quality standards training homecare mental health safety risk management TPBN1_IJ
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