113 Quality Manager jobs in Ireland
Manager, Quality Control
Sligo, Connacht
AbbVie
Posted today
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
0
Senior Manager, Quality Control Laboratory
Westport, Connacht
AbbVie
Posted today
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are currently looking for a Senior Manager of Quality Control Laboratories to join our team in Westport on a 12-month fixed-term contract. The Senior Manager of Quality Control is responsible for strategy, planning, and management of laboratory operations, ensuring compliance with FDA, HPRA, and EPA safety standards and budgetary constraints. This role supports the QA site head in achieving operational goals.
Responsibilities:
+ Manage and motivate employees, ensuring capacity aligns with business needs.
+ Develop and deliver business plans, manage departmental budget, and handle new product implementation.
+ Represent the company in client and regulatory meetings, ensuring GMP compliance.
+ Organize cross-functional activities to improve lab efficiencies.
+ Coordinate meetings and manage documentation and compliance tools.
Qualifications
+ Proven track record in people and operations management within Pharma/Medical Devices/Food industry.
+ Qualification in Pharmaceutical Science.
+ Excellent conflict resolution, planning, and communication skills.
+ Ability to manage in regulated environments and adapt to changes.
+ Strong commitment to AbbVie's values and business ethics.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are currently looking for a Senior Manager of Quality Control Laboratories to join our team in Westport on a 12-month fixed-term contract. The Senior Manager of Quality Control is responsible for strategy, planning, and management of laboratory operations, ensuring compliance with FDA, HPRA, and EPA safety standards and budgetary constraints. This role supports the QA site head in achieving operational goals.
Responsibilities:
+ Manage and motivate employees, ensuring capacity aligns with business needs.
+ Develop and deliver business plans, manage departmental budget, and handle new product implementation.
+ Represent the company in client and regulatory meetings, ensuring GMP compliance.
+ Organize cross-functional activities to improve lab efficiencies.
+ Coordinate meetings and manage documentation and compliance tools.
Qualifications
+ Proven track record in people and operations management within Pharma/Medical Devices/Food industry.
+ Qualification in Pharmaceutical Science.
+ Excellent conflict resolution, planning, and communication skills.
+ Ability to manage in regulated environments and adapt to changes.
+ Strong commitment to AbbVie's values and business ethics.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
1
Quality Manager
Abbott
Posted today
Job Viewed
Job Description
**About Abbott**
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
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
This advertiser has chosen not to accept applicants from your region.
2
Quality Manager
Dublin, Leinster
PM Group
Posted today
Job Viewed
Job Description
Overview PM Group's OTS (Outsourced Technical Services) department are currently seeking to recruit a Quality Manager to be based in our clients Medical Devices facility based in South Dublin. The successful candidate will be responsible for leading critical projects for new product introduction. This involves providing leadership to the Quality Engineering team (5-7 associates) , managing validation studies, and working closely with various internal and external stakeholders Responsibilities Responsibilities: Support ISO9000/ISO13485 Quality Systems : Ensuring the company's quality management system aligns with these international standards, which are crucial in the medical devices/pharmaceutical Regulatory Compliance : Ensuring that all activities meet embecta's and external regulatory requirements. Leadership Role : Being a key member of the Quality Leadership Team, leading the Quality Engineering Team through daily management, performance reviews, and delegation. Continuous Improvement : Supporting programs like Six Sigma to enhance processes and product quality. Quality System Management : Overseeing systems related to production support, such as non-conformance, incident reporting, and customer complaint analysis. Customer Interaction : Liaising with key external customers, to ensure that quality standards meet customer expectations. CAPA Management : Ensuring Corrective and Preventive Actions (CAPAs) are completed in compliance with regulatory standards. GMP Oversight : Ensuring Good Manufacturing Practice (GMP) compliance in Production and Quality Engineering activities. Documentation : Preparing and maintaining documentation to meet regulatory requirements. Qualifications Educational Requirements and Relevant Experience: Industry Experience : At least 5 years in an ISO environment, preferably in the medical devices or pharmaceutical industry. Supervisory Experience : A minimum of 3 years in a supervisory role, indicating the need for leadership skills. Knowledge, Skills and Abilities: Technical Knowledge : Understanding of Statistical Process Control (SPC) and Six Sigma methodologies, with Greenbelt Certification being advantageous. Advanced Technical writing skills are required. Regulatory Knowledge : Experience with FDA requirements and audit Process Expertise : Experience in process validation, sterilization, and cleanroom environments is a plus. #LI-MD1
This advertiser has chosen not to accept applicants from your region.
3
Quality Manager
Dublin, Leinster
Life Science Recruitment Ltd
Posted today
Job Viewed
Job Description
Were currently recruiting for an exciting opportunity with a Quality & Compliance Consultancy based in Dublin. This is a key role ensuring compliance with EU Cosmetics Regulation while supporting the release of high-quality products to market. Key Responsibilities: Act as Responsible Person under EU Cosmetics Regulation. Oversee product release and ensure compliance with all regulatory requirements. Manage and audit Contract Manufacturing Organisations (CMOs) to maintain quality standards. Liaise with EU regulatory bodies and ensure timely submissions and approvals. Lead quality management systems, product safety reviews, and continuous improvement initiatives. Education & Experience Requirements: Proven experience in cosmetics industry. Demonstrated background as RP or equivalent within the EU cosmetics sector. Strong knowledge of GMP and EU Cosmetics Regulation. Experience managing CMOs and product release. Excellent communication and leadership skills. If interested in this posting please feel free to contact Sen McCarthy on or for further information.
This advertiser has chosen not to accept applicants from your region.
4
Quality Manager
Waterford, Munster
RPG Recruitment
Posted today
Job Viewed
Job Description
Quality Systems Manager required by FMCG company based in South Tipperary. Reporting to the Technical Manager, The overall purpose of this role is To ensure that all Quality systems and procedures are in line with Industry best practices and Customer requirements and are audited and verified to this standard Responsibilities of this role Responsible for the updating, implementation and maintenance of food quality and food safety systems in conjunction with the Quality team. Internal auditing of systems to comply with BRC and customer requirements Document & data control of all manuals and records in QS. Management of corrective and preventative system. HACCP Review and review of Quality Management System. Work closely with customer technical contacts as required to ensure specification and artwork meets customer & legal requirements, attend weekly meetings. Supplier approval ensuring packaging, raw material, intermediate, factored good specifications maintained up to date and on file including customer 3rd party certification cert and reports responsible for maintaining approved supplier list & supporting documentation. Active participation in preparation and on the day handling of customer & 3rd party audits / Visits etc. Support for Mass Balance / Traceability exercises as required. Pro-active in taking ownership of technical / quality projects as requested with excellent follow through to completion and attention to detail. Attend relevant training courses as well as customer database training courses as recommended by the Technical Manager Attend all meetings as requested by the Technical Manager and engage positively and contribute to same. Support of Lean programs The ideal candidate will have BSc in food science or similar Ideally 3 to 5 years QA/QC experience in Food Manufacturing environment Be self-motivated Be flexible Have the ability to work on ones own initiative Be a keen team player Have good communication skills (verbal & written Benefits: Pension
This advertiser has chosen not to accept applicants from your region.
5
Quality Manager
Shannon, Munster
Harmonics
Posted today
Job Viewed
Job Description
Join our client, a recognised leader in the precision engineering and medical device manufacturing industry. In this role, you will be part of a dynamic, forward-thinking team dedicated to delivering world-class quality, compliance, and innovation. Reporting to:Quality Director Job Purpose: To provide technical guidance, structure, and leadership for the Quality function, ensuring that the site meets and exceeds the business and quality plans. Responsibilities: Ensure compliance of quality systems with the QSR and all current pertinent regulations. (e.g. FDA, ISO). Act as a management representative for the standards in place within the company. Promote the awareness of applicable regulatory requirements and quality management system requirements throughout the company to drive improvements to overall quality and compliance. Participation, co-ordination and maintenance of the internal audit process. Identifying and analysing non-conformances and related trends. Ensuring issues are highlighted and escalated to Senior Management for corrective and preventive action facilitating business improvement. Promote awareness of customer requirements within the company. Support the training management process. Lead the implementation of Quality improvement projects. Contribute to Lean initiatives within the Quality function and across broader business operations. Technical Leadership. Participate in the interpretation of Engineering drawings. Provide support to the measurement system analysis process. Provide support to the inspection process and participate in the review of inspection reports. Provide support with the preventive maintenance and calibration systems. Provide support to the scrap analysis process. Participate in ongoing problem solving and on corrective action teams. Review and approve CAPA actions in conjunction with Quality Systems. Utilise Minitab and other statistical tools to perform root cause analysis, process capability studies, and data-driven decision-making. Lead statistical analysis initiatives to identify trends, reduce variability, and improve product and process quality. Participate in producing daily management reports with a view to identifying and making recommendations on improvement opportunities. Experience: Bachelors degree in a scientific discipline is an advantage. Advantage of having a minimum 5 years of quality management experience or equivalent in the medical device industry and/or FDA regulated environment. Must have experience in people leadership role (at least 3 to 5 years). Demonstrated knowledge of Quality Assurance. Excellent communication skills, including the ability to communicate to all levels of an organization. Excellent analytical and problem-solving skills. Demonstrated ability to collaborate with cross functional teams to ensure business success and ensuring compliance. Strong leadership skills, including influencing and team development. Thorough knowledge of QSR and ISO quality system requirements. Lead Auditor certification. Solid experience in medical device operations with a strong background in QA along with excellent communications and people management. If you are living in Ireland and hold a VALID WORK PERMIT, we would love to hear from you, if however, you do not hold a valid work permit unfortunately we will not be in a position to assist you with your job search. Skills: Regulatory & Quality Systems Expertise Statistical & Analytical Skills Quality Assurance Leadership in Medical Devices
This advertiser has chosen not to accept applicants from your region.
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6
Quality manager
Clare, Munster
Harmonics
Posted today
Job Viewed
Job Description
Join our client, a recognised leader in the precision engineering and medical device manufacturing industry.
In this role, you will be part of a dynamic, forward-thinking team dedicated to delivering world-class quality, compliance, and innovation.
Reporting to: Quality Director Job Purpose: To provide technical guidance, structure, and leadership for the Quality function, ensuring that the site meets and exceeds the business and quality plans.
Responsibilities: Ensure compliance of quality systems with the QSR and all current pertinent regulations.
(e.g. FDA, ISO). Act as a management representative for the standards in place within the company.
Promote the awareness of applicable regulatory requirements and quality management system requirements throughout the company to drive improvements to overall quality and compliance.
Participation, co-ordination and maintenance of the internal audit process.
Identifying and analysing non-conformances and related trends.
Ensuring issues are highlighted and escalated to Senior Management for corrective and preventive action facilitating business improvement.
Promote awareness of customer requirements within the company.
Support the training management process.
Lead the implementation of Quality improvement projects.
Contribute to Lean initiatives within the Quality function and across broader business operations.
Technical Leadership.
Participate in the interpretation of Engineering drawings.
Provide support to the measurement system analysis process.
Provide support to the inspection process and participate in the review of inspection reports.
Provide support with the preventive maintenance and calibration systems.
Provide support to the scrap analysis process.
Participate in ongoing problem solving and on corrective action teams.
Review and approve CAPA actions in conjunction with Quality Systems.
Utilise Minitab and other statistical tools to perform root cause analysis, process capability studies, and data-driven decision-making.
Lead statistical analysis initiatives to identify trends, reduce variability, and improve product and process quality.
Participate in producing daily management reports with a view to identifying and making recommendations on improvement opportunities.
Experience: Bachelors degree in a scientific discipline is an advantage.
Advantage of having a minimum 5 years of quality management experience or equivalent in the medical device industry and/or FDA regulated environment.
Must have experience in people leadership role (at least 3 to 5 years).
Demonstrated knowledge of Quality Assurance.
Excellent communication skills, including the ability to communicate to all levels of an organization.
Excellent analytical and problem-solving skills.
Demonstrated ability to collaborate with cross functional teams to ensure business success and ensuring compliance.
Strong leadership skills, including influencing and team development.
Thorough knowledge of QSR and ISO quality system requirements.
Lead Auditor certification.
Solid experience in medical device operations with a strong background in QA along with excellent communications and people management.
If you are living in Ireland and hold a VALID WORK PERMIT, we would love to hear from you, if however, you do not hold a valid work permit unfortunately we will not be in a position to assist you with your job search.
Skills: Regulatory & Quality Systems Expertise Statistical & Analytical Skills Quality Assurance Leadership in Medical Devices
In this role, you will be part of a dynamic, forward-thinking team dedicated to delivering world-class quality, compliance, and innovation.
Reporting to: Quality Director Job Purpose: To provide technical guidance, structure, and leadership for the Quality function, ensuring that the site meets and exceeds the business and quality plans.
Responsibilities: Ensure compliance of quality systems with the QSR and all current pertinent regulations.
(e.g. FDA, ISO). Act as a management representative for the standards in place within the company.
Promote the awareness of applicable regulatory requirements and quality management system requirements throughout the company to drive improvements to overall quality and compliance.
Participation, co-ordination and maintenance of the internal audit process.
Identifying and analysing non-conformances and related trends.
Ensuring issues are highlighted and escalated to Senior Management for corrective and preventive action facilitating business improvement.
Promote awareness of customer requirements within the company.
Support the training management process.
Lead the implementation of Quality improvement projects.
Contribute to Lean initiatives within the Quality function and across broader business operations.
Technical Leadership.
Participate in the interpretation of Engineering drawings.
Provide support to the measurement system analysis process.
Provide support to the inspection process and participate in the review of inspection reports.
Provide support with the preventive maintenance and calibration systems.
Provide support to the scrap analysis process.
Participate in ongoing problem solving and on corrective action teams.
Review and approve CAPA actions in conjunction with Quality Systems.
Utilise Minitab and other statistical tools to perform root cause analysis, process capability studies, and data-driven decision-making.
Lead statistical analysis initiatives to identify trends, reduce variability, and improve product and process quality.
Participate in producing daily management reports with a view to identifying and making recommendations on improvement opportunities.
Experience: Bachelors degree in a scientific discipline is an advantage.
Advantage of having a minimum 5 years of quality management experience or equivalent in the medical device industry and/or FDA regulated environment.
Must have experience in people leadership role (at least 3 to 5 years).
Demonstrated knowledge of Quality Assurance.
Excellent communication skills, including the ability to communicate to all levels of an organization.
Excellent analytical and problem-solving skills.
Demonstrated ability to collaborate with cross functional teams to ensure business success and ensuring compliance.
Strong leadership skills, including influencing and team development.
Thorough knowledge of QSR and ISO quality system requirements.
Lead Auditor certification.
Solid experience in medical device operations with a strong background in QA along with excellent communications and people management.
If you are living in Ireland and hold a VALID WORK PERMIT, we would love to hear from you, if however, you do not hold a valid work permit unfortunately we will not be in a position to assist you with your job search.
Skills: Regulatory & Quality Systems Expertise Statistical & Analytical Skills Quality Assurance Leadership in Medical Devices
This advertiser has chosen not to accept applicants from your region.
7
Quality manager
Dublin, Leinster
PM Group
Posted today
Job Viewed
Job Description
Overview PM Group's OTS (Outsourced Technical Services) department are currently seeking to recruit a Quality Manager to be based in our clients Medical Devices facility based in South Dublin.
The successful candidate will be responsible for leading critical projects for new product introduction.
This involves providing leadership to the Quality Engineering team (5-7 associates) , managing validation studies, and working closely with various internal and external stakeholders Responsibilities Responsibilities: Support ISO9000/ISO13485 Quality Systems : Ensuring the company's quality management system aligns with these international standards, which are crucial in the medical devices/pharmaceutical Regulatory Compliance : Ensuring that all activities meet embecta's and external regulatory requirements.
Leadership Role : Being a key member of the Quality Leadership Team, leading the Quality Engineering Team through daily management, performance reviews, and delegation.
Continuous Improvement : Supporting programs like Six Sigma to enhance processes and product quality.
Quality System Management : Overseeing systems related to production support, such as non-conformance, incident reporting, and customer complaint analysis.
Customer Interaction : Liaising with key external customers, to ensure that quality standards meet customer expectations.
CAPA Management : Ensuring Corrective and Preventive Actions (CAPAs) are completed in compliance with regulatory standards.
GMP Oversight : Ensuring Good Manufacturing Practice (GMP) compliance in Production and Quality Engineering activities.
Documentation : Preparing and maintaining documentation to meet regulatory requirements.
Qualifications Educational Requirements and Relevant Experience: Industry Experience : At least 5 years in an ISO environment, preferably in the medical devices or pharmaceutical industry.
Supervisory Experience : A minimum of 3 years in a supervisory role, indicating the need for leadership skills.
Knowledge, Skills and Abilities: Technical Knowledge : Understanding of Statistical Process Control (SPC) and Six Sigma methodologies, with Greenbelt Certification being advantageous.
Advanced Technical writing skills are required.
Regulatory Knowledge : Experience with FDA requirements and audit Process Expertise : Experience in process validation, sterilization, and cleanroom environments is a plus.
#LI-MD1
The successful candidate will be responsible for leading critical projects for new product introduction.
This involves providing leadership to the Quality Engineering team (5-7 associates) , managing validation studies, and working closely with various internal and external stakeholders Responsibilities Responsibilities: Support ISO9000/ISO13485 Quality Systems : Ensuring the company's quality management system aligns with these international standards, which are crucial in the medical devices/pharmaceutical Regulatory Compliance : Ensuring that all activities meet embecta's and external regulatory requirements.
Leadership Role : Being a key member of the Quality Leadership Team, leading the Quality Engineering Team through daily management, performance reviews, and delegation.
Continuous Improvement : Supporting programs like Six Sigma to enhance processes and product quality.
Quality System Management : Overseeing systems related to production support, such as non-conformance, incident reporting, and customer complaint analysis.
Customer Interaction : Liaising with key external customers, to ensure that quality standards meet customer expectations.
CAPA Management : Ensuring Corrective and Preventive Actions (CAPAs) are completed in compliance with regulatory standards.
GMP Oversight : Ensuring Good Manufacturing Practice (GMP) compliance in Production and Quality Engineering activities.
Documentation : Preparing and maintaining documentation to meet regulatory requirements.
Qualifications Educational Requirements and Relevant Experience: Industry Experience : At least 5 years in an ISO environment, preferably in the medical devices or pharmaceutical industry.
Supervisory Experience : A minimum of 3 years in a supervisory role, indicating the need for leadership skills.
Knowledge, Skills and Abilities: Technical Knowledge : Understanding of Statistical Process Control (SPC) and Six Sigma methodologies, with Greenbelt Certification being advantageous.
Advanced Technical writing skills are required.
Regulatory Knowledge : Experience with FDA requirements and audit Process Expertise : Experience in process validation, sterilization, and cleanroom environments is a plus.
#LI-MD1
This advertiser has chosen not to accept applicants from your region.
8
Quality manager
Waterford, Munster
RPG Recruitment
Posted today
Job Viewed
Job Description
Quality Systems Manager required by FMCG company based in South Tipperary.
Reporting to the Technical Manager, The overall purpose of this role is To ensure that all Quality systems and procedures are in line with Industry best practices and Customer requirements and are audited and verified to this standard Responsibilities of this role Responsible for the updating, implementation and maintenance of food quality and food safety systems in conjunction with the Quality team.
Internal auditing of systems to comply with BRC and customer requirements Document & data control of all manuals and records in QS.
Management of corrective and preventative system.
HACCP Review and review of Quality Management System.
Work closely with customer technical contacts as required to ensure specification and artwork meets customer & legal requirements, attend weekly meetings.
Supplier approval ensuring packaging, raw material, intermediate, factored good specifications maintained up to date and on file including customer 3rd party certification cert and reports responsible for maintaining approved supplier list & supporting documentation.
Active participation in preparation and on the day handling of customer & 3rd party audits / Visits etc.
Support for Mass Balance / Traceability exercises as required.
Pro-active in taking ownership of technical / quality projects as requested with excellent follow through to completion and attention to detail.
Attend relevant training courses as well as customer database training courses as recommended by the Technical Manager Attend all meetings as requested by the Technical Manager and engage positively and contribute to same.
Support of Lean programs The ideal candidate will have BSc in food science or similar Ideally 3 to 5 years QA/QC experience in Food Manufacturing environment Be self-motivated Be flexible Have the ability to work on ones own initiative Be a keen team player Have good communication skills (verbal & written Benefits: Pension
Reporting to the Technical Manager, The overall purpose of this role is To ensure that all Quality systems and procedures are in line with Industry best practices and Customer requirements and are audited and verified to this standard Responsibilities of this role Responsible for the updating, implementation and maintenance of food quality and food safety systems in conjunction with the Quality team.
Internal auditing of systems to comply with BRC and customer requirements Document & data control of all manuals and records in QS.
Management of corrective and preventative system.
HACCP Review and review of Quality Management System.
Work closely with customer technical contacts as required to ensure specification and artwork meets customer & legal requirements, attend weekly meetings.
Supplier approval ensuring packaging, raw material, intermediate, factored good specifications maintained up to date and on file including customer 3rd party certification cert and reports responsible for maintaining approved supplier list & supporting documentation.
Active participation in preparation and on the day handling of customer & 3rd party audits / Visits etc.
Support for Mass Balance / Traceability exercises as required.
Pro-active in taking ownership of technical / quality projects as requested with excellent follow through to completion and attention to detail.
Attend relevant training courses as well as customer database training courses as recommended by the Technical Manager Attend all meetings as requested by the Technical Manager and engage positively and contribute to same.
Support of Lean programs The ideal candidate will have BSc in food science or similar Ideally 3 to 5 years QA/QC experience in Food Manufacturing environment Be self-motivated Be flexible Have the ability to work on ones own initiative Be a keen team player Have good communication skills (verbal & written Benefits: Pension
This advertiser has chosen not to accept applicants from your region.
9