46 Quality Assurance And Engineering jobs in Dublin.

Hiring now: Sr Engr Process Developme @ Amgen, Multiple Manufacturing Po @ Baxter, Qc Ops Sr Spec @ Astrazenec, Sr Human Factors Engr @ Mallinckro, Qc Sr Analyst @ Alexion, Mgr Pharmaceutical Develo @ Jazz Pharm, Associate Dir Global Deve @ Regeneron , Associate Dir It Complian @ Iqvia, Regulatory Affairs Mgr Cm @ Parexel, Sr Deltav Engr @ Cognizant.Explore more at jobswithgpt.com.

🔥 Skills

GMP (9) Project Management (8) cGMP (7) continuous improvement (6) Quality Assurance (6) Regulatory Compliance (6) cross-functional teams (5) Compliance (5) Quality Control (5) Quality (4)

đź“Ť Locations

Dublin (39) DĂşn Laoghaire (4) Bray (3)
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Amgen

Sr. Engineer Process Development DĂşn Laoghaire
Skills & Focus: Process Development, Single use technologies, Drug product, Filling processes, cGMP, Technical Writing, Risk assessment, Syringe filling, Technical support, Quality systems
About the Company: Amgen is a biotechnology company that develops innovative human therapeutics.
Experience: 5 years experience in a similar role OR Master’s degree & 3 years of directly related experience OR Associate’s degree & 10 years of directly related experience.
Type: Full time
Senior Automation Engineer DĂşn Laoghaire
Skills & Focus: automation systems, GMP-regulated, incident investigations, continuous improvements, engineering assessments, PLC programming, HMI, SCADA, biopharmaceutical, quality assurance
About the Company: Amgen discovers, develops, and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realise the …
Experience: 5+ years experience in operations/manufacturing environment
Type: Full-time
Sr. Engineer Process Development DĂşn Laoghaire
Skills & Focus: Process Development, technical expertise, drug product formulation, lyophilization, change control, continuous improvement, GMP documentation, cross-functional teams, leadership, problem-solving
Experience: 6 years or PhD with 4 years
Type: Full time

Baxter

Multiple Manufacturing Positions Dublin
Skills & Focus: Manufacturing, Production, Technical, Engineering, Quality, Medical Devices, Healthcare, Innovation, Team Leader, Compliance
About the Company: Baxter is a global leader in medical devices and solutions, committed to saving and sustaining lives through innovation in healthcare options.
Type: Full time

Astrazeneca

QC Operations, Senior Specialist Dublin
Skills & Focus: QC operations, analytical investigations, deviations, method troubleshooting, cGMP, biopharmaceuticals, regulatory support, cross-functional teams, analytical chemistry, audit readiness
About the Company: AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines, pri…
Experience: 5-8 years experience within a biotech pharmaceutical or biopharmaceutical manufacturing environment
Type: Full-time

Mallinckrodt

Senior Human Factors Engineer Dublin
Skills & Focus: human factors, design validation, medical devices, ISO62366, FDA guidance, formative evaluation, contextual inquiry, validation studies, risk analysis, usability studies
Experience: 5+ years experience on medical system design validation, with 2+ years experience with end users / patient in hospital environment.

Alexion

QC Senior Analyst Dublin
Skills & Focus: Quality Control, Microbiology, Environmental Monitoring, cGMP, Regulatory Requirements, Validation, Testing, Laboratory, Problem Solving, Root Cause Analysis
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in all that we d…
Experience: Minimum of 3 years experience in cGMP Quality environment.
Type: Contract

Baxter

Various Positions in Dublin Dublin
Skills & Focus: Quality, Manufacturing, Customer Service, Production, Technician, Medical, Contract, Pharmaceuticals, Innovation, Healthcare
About the Company: Baxter is a global company dedicated to improving patient care and outcomes through a diverse range of innovative healthcare products and services.
Type: Full-time
Benefits: Comprehensive benefits options reflecting the value placed on employees.

Astrazeneca

Senior Specialist, Patient Safety Dublin
Skills & Focus: Pharmacovigilance, Patient Safety, health authority regulations, internal audits, external health authority inspections, Argus, Veeva Vault, vendor management, data analytics, cross-functional collaboration
About the Company: AstraZeneca is a science-led, global biopharmaceutical company, committed to improving the health and lives of people across the globe through our research and…
Experience: Understanding of local UK, Ireland and Malta health authority regulations. Experience in internal audits / external health authority inspections. Experience in using Pharmacovigilance systems such as Argus and Veeva Vault modules.

Alexion

Senior Packaging Design Engineer Dublin
Skills & Focus: packaging design, GMP compliance, component design, labeling and packaging, lean manufacturing, collaboration, CAD drawings, regulatory submissions, team leadership, process improvements
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in all that we d…
Experience: A minimum of 5 years’ experience with licensed products and facilities with responsibility for labeling and packaging operations required.

Jazz Pharmaceuticals

Mgr, Pharmaceutical Development Quality Assurance Dublin
Skills & Focus: Pharmaceutical Development, Quality Assurance, GMP, Clinical Trials, Investigational Medicinal Products, Vendor Auditing, Regulatory Submissions, Quality Systems, SOPs, Continuous Improvement
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Benefits: medical, dental and vision insurance, retirement savings plan, and flexible paid vacation

Regeneron Pharmaceuticals Inc.

Associate Director, Global Development Quality Management (GCP) Dublin
Skills & Focus: quality management, compliance, quality assurance, audits, training, data analysis, industry standards, production, collaboration, proactive
About the Company: Regeneron is committed to excellence in quality management and ensuring the highest standards across its products and services.
Experience: At least 5 years of experience in a quality management role.
Type: Contract
Benefits: Health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees.

Iqvia

Associate Director, IT Compliance Dublin
Skills & Focus: IT Compliance, Validation, GxP, regulations, risk management, audit, client service, regulatory guidance, Foster system lifecycle, Quality Assurance
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Substantial experience in healthcare, life sciences (Pharma, CROs), related product or service industry.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Alexion

Senior Manager - Supplier Quality (Materials) Dublin
Skills & Focus: Supplier Quality, Material Qualification, Quality Risk Management, Compliance, Project Management, Regulatory Inspections, Cross-functional Teams, Stakeholder Management, Process Improvement, Quality Metrics
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in all that we d…
Experience: Minimum of 6+ years’ experience in Quality with medical device, pharmaceutical, or biologics experience.
Bio-Process Technician Dublin
Skills & Focus: cGMP, biotech, SOPs, batch records, bioreactors, data automation, Lean Tools, continuous improvement, troubleshooting, pharmaceutical manufacturing
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in all that we d…
Experience: 5+ years’ external experience in a cGMP biotech or closely allied pharmaceutical manufacturing environment

Parexel

Regulatory Affairs Manager - CMC biologics Dublin
Skills & Focus: Regulatory Affairs, CMC, Life Sciences, Biopharmaceuticals, Quality Assurance, Submission Strategies, Technical Documentation, Project Management, Risk Mitigation, Collaboration
About the Company: Parexel is a global biopharmaceutical services organization that provides expertise and solutions to companies in the life sciences sector, helping them to nav…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, opportunities for career growth, and a supportive work environment.

Cognizant

Senior DeltaV Engineer Dublin
Skills & Focus: DeltaV, Automation Engineer, pharmaceutical, commissioning, Project Management, Configuration, Testing, Installation Qualification, operational Qualification, client interaction
About the Company: Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. …
Experience: 3+ years pharmaceutical manufacturing experience.
Type: Full-time
Benefits: Comprehensive total rewards package, including a competitive salary and pension plan with matching contributions, flexi…

Astrazeneca

Specialist, Technical Services Drug Product Dublin
Skills & Focus: pharmaceutical manufacturing, technology transfer, process validation, continuous improvement, cGMP requirements, regulatory submissions, process optimization, yield improvement, lean six sigma, cross-functional relationships
About the Company: AstraZeneca is a global, science-led biopharmaceutical business and our innovative medicines are used by millions of patients worldwide.
Experience: 3-5 years’ experience in a technical or manufacturing role in the pharmaceutical industry
Type: Full-time

Emergent Biosolutions

Sr. Engineer, Design Assurance, Risk Management, Human Factors Engineering Dublin
Skills & Focus: Design Assurance, Risk Management, Human Factors Engineering, Medical Device, Combination Products, Technical Documentation, ISO 13485, ISO 14971, Regulatory Compliance, Design Control
About the Company: Emergent BioSolutions is focused on protecting and enhancing lives by developing products designed to meet public health challenges.

Jazz Pharmaceuticals

Senior Quality Assurance Specialist (Drug Substance) Dublin
Skills & Focus: Quality Assurance, GMP, Regulatory Compliance, Contract Manufacturing, Biologics, Drug Substance, Audits, Investigations, Vendor Management, Quality Technical Agreements
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Experience: >5 years

Mcdermott Laboratories Limited

Senior Lab Equipment and System Engineer Dublin
Skills & Focus: Equipment Installation, Qualification, Computer System Validation, Preventative Maintenance, Calibration, Quality Management System, Troubleshooting, ISO 13485, FDA, Data Integrity
About the Company: At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolv…
Experience: At least 4 years’ experience in a GMP or ISO 13485 accredited laboratory
Benefits: Excellent career progression opportunities, work-life balance initiatives, bonus scheme, health insurance, pension.

Astrazeneca

QC Senior Analyst Dublin
Skills & Focus: Quality Control, Microbiology, cGMP, Environmental Monitoring, Biopharmaceuticals, Validation, Testing, Compliance, Root Cause Analysis, Training
About the Company: AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines.
Experience: Minimum of 3 years experience in cGMP Quality environment.
Type: Contract

Cognizant

Senior Engineer Dublin
Skills & Focus: LabTech, IT validation, system lifecycle management, software configuration, risk assessment, GxP, Active Directory, data management, regulatory compliance, project management
About the Company: Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, …
Experience: 5+ years in IT validation engineer role focused on laboratory systems
Type: Full-time

Jazz Pharmaceuticals

Director, Pharmaceutical Development QA Dublin
Skills & Focus: Pharmaceutical Development, Quality Assurance, Qualified Person, GMP, Quality Systems, Clinical Phases, Regulatory Compliance, Quality Oversight, Technical Support, Cross-functional Collaboration
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Experience: 10+ years of practical experience in the Pharmaceutical Industry in QA or QC roles

Perrigo

Director of Global Quality Management Systems Dublin
Skills & Focus: Quality Management Systems, Deviations, CAPA, Change Control, Quality Assurance, Quality Control, Pharmaceutical Industry, Regulatory Standards, Corrective Actions, Root Cause Analysis
About the Company: Perrigo is dedicated to providing The Best Self-Care for Everyone and is a top player in the European Consumer Self-Care market, as well as the largest U.S. st…
Experience: Minimum of 10 years in quality systems, quality assurance, quality control, or risk management within the pharmaceutical industry or equivalent.
Type: Full-time
Benefits: Alongside competitive compensation, Perrigo offers benefits tailored to support employees and their families, with care…

Mcdermott Laboratories Limited

Senior Quality Assurance Specialist, Device Development Assurance Dublin
Skills & Focus: Quality Management System, GMP, ISO13485, Computer System Validation, Laboratory Equipment Qualification, Quality Oversight, Data Integrity, Preventative Maintenance, Test Method Validation, Stability Product Management
About the Company: At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolv…
Experience: Minimum 3-5 years relevant professional experience (GMP / Medical Device Industry quality operations)
Salary: Competitive salary
Benefits: Excellent career progression opportunities, Work-life balance initiatives, Bonus scheme, Health insurance, Pension

Biomarin

Director, Drug Product Technology Transfer Dublin
Skills & Focus: Drug Product Technology Transfer, cGMP, Quality Systems, Project Execution, Process Development, Technical Leadership, Team Management, Regulatory Filing, Collaboration, Biopharma
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: 10+ years of professional experience in the pharmaceutical industry, including managerial experience
Type: Hybrid

Regeneron Pharmaceuticals

Senior Manager, GD Quality Management (GCP) Dublin
Skills & Focus: Quality Management, GCP, compliance, clinical trials, risk management, stakeholders, audit, quality assurance, Corrective Action/Preventive Action, training
Experience: 8 years in healthcare/pharmaceutical industry
Salary: $132,400.00 - $216,000.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Novartis

Associate Director, Clinical QA Dublin
Skills & Focus: Quality oversight, clinical trials, Good Clinical Practice, quality risk management, stakeholder collaboration, quality incident management, audits, inspections, CAPA, continuous improvement
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Type: Hybrid Working

Parexel

Regulatory Affairs Manager - CMC biologics Dublin
Skills & Focus: Regulatory Affairs, CMC, Biologics, Pharmaceuticals, Submission Strategies, Quality Control, Risk Management, Project Management, Technical Documentation, Collaboration
About the Company: Parexel is a global biopharmaceutical services company that helps clients navigate the complex and ever-changing regulatory landscape.
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote/Office-based

Jabil

Project Engineer (Packaging) Dublin
Skills & Focus: automation, packaging, medical devices, manufacturing, cross-functional teams, project management, optimization, continuous improvement, statistical analysis, regulatory compliance
About the Company: At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive eng…
Experience: 4+ years’ experience in a manufacturing environment with high-volume automated assembly and packaging experience is preferable.
Type: Full time

Jazz Pharmaceuticals

Associate Director, Packaging Technology Dublin
Skills & Focus: packaging, pack design, validation, serialization, project management, cross functional teams, quality, regulatory, stakeholder management, team development
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Experience: minimum of 10 years’ experience in the field
Type: Full-time

Baxter

Quality Assurance Batch Releaser Dublin
Skills & Focus: Quality, Assurance, Batch Releaser, Pharmaceuticals, Healthcare, Compliance, Manufacturing, Innovation, Production, Diagnostics
About the Company: Baxter is a global medical products company that focuses on saving and sustaining lives by providing essential healthcare solutions.
Type: Full time
Benefits: Comprehensive benefits options reflecting the value placed in employees.

Viatris

Lab Equipment and Systems Engineer, Device Product Performance Dublin
Skills & Focus: Device Development, Quality Management System, ISO 13485, GMP, Computer System Validation, Preventative Maintenance, Calibration, Regulatory standards, Troubleshooting, Data Integrity
About the Company: Viatris empowers people worldwide to live healthier at every stage of life. Through Access, Leadership, and Partnership, Viatris provides high quality trusted …
Experience: At least 4 years’ experience in a GMP or ISO 13485 accredited laboratory.
Benefits: Excellent career progression opportunities, Work-life balance initiatives, Bonus scheme, Health insurance, Pension.

Perrigo

Director Global Quality Risk Management Dublin
Skills & Focus: Quality Risk Management, GMP, regulatory requirements, quality management systems, risk assessment, risk control, risk review, stakeholder management, analytical skills, communication skills
About the Company: Perrigo is a leading global provider of OTC health and wellness solutions, dedicated to enhancing the wellbeing of consumers through trusted self-care products.
Experience: Minimum of 10 years of experience in quality risk management, quality assurance, and quality control within the pharmaceutical industry or equivalent
Type: Hybrid Working Approach
Benefits: Alongside competitive compensation, benefits tailored to supporting you and your family, as well as career development …

Baxter

Quality Systems Specialist Dublin
Skills & Focus: Quality Management, Good Manufacturing Practice, Regulatory Compliance, Documentation Management, Training, Audits, Continuous Improvement, Risk Assessments, Customer Complaints, Supplier Management
About the Company: Baxter is a global healthcare company that provides a wide range of medical products and therapies to save and sustain lives. They are deeply connected to thei…
Experience: Post qualification experience of at least 1 years in a GMP environment, ideally in a quality role
Type: Contract
Benefits: Pension, Health Insurance, Life Assurance, Paid Time Off, Continuing Education/Professional Development

Cognizant

FLS Engineer Dublin
Skills & Focus: Automation, Delta V, GMP, Engineering, PLC, SCADA, Continuous Improvement, cGMP, Problem Management, Technical Skills
About the Company: Cognizant is a leading professional services company transforming clients' business, operating, and technology models for the digital era. With a unique consul…
Experience: 4+ Years Automation Experience in a GMP environment
Type: Full-time

Johnson & Johnson

Senior Project Manager, Quality Standards Dublin
Skills & Focus: Project Management, Quality Standards, Regulatory Compliance, Medical Device, Pharmaceuticals, Team Leadership, Risk Management, Quality Management Systems, Communication Skills, Strategic Planning
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Minimum of 8 years in the medical device or pharmaceutical industries
Type: Hybrid

Cai

Project Manager – CQV Engineer Dublin
Skills & Focus: CQV, Quality Control, Validation, Project Management, GMP, FDA, Regulatory Compliance, Risk Assessment, Team Leadership, Cross-functional Team
About the Company: CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 700 employees worldwide. We provide commissioning, qualificat…
Experience: 8+ years of experience in CQV, project management, or quality control within pharmaceutical, biotech, or life sciences industries.
Type: Full Time
Benefits: Professional growth, collaboration, and hands-on learning in an employee-owned environment.

Perrigo

Senior QA Auditor Dublin
Skills & Focus: QA Auditor, pharmaceutical experience, supplier audits, contract manufacturers, GMP, analytical skills, IRCA certified, MS Office, independent management, international travel
About the Company: Perrigo is a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter products and infant formula.
Experience: 5+ years pharmaceutical experience (quality and/or auditing)
Type: Hybrid
Benefits: Competitive compensation and benefits tailored to supporting you and your family.

Cognizant

LabTech IT - Senior Engineer Dublin
Skills & Focus: IT validation, laboratory systems, Pharmaceutical, biopharma, GxP, risk assessments, configuration, system administration, documentation, change control
About the Company: Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, …
Experience: 5+ years of experience in IT validation engineer role with a focus on laboratory systems in the Pharmaceutical Biopharma and healthcare Industry.
Type: Full-time

Cai

Qualified Person (QP) Dublin
Skills & Focus: Qualified Person, certifying medicinal products, quality compliance guidance, quality management system, GMP compliance, pharmaceutical manufacturing, deviation management, audit support, cross functional teams, pharmaceutical legislation
About the Company: CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 850 people worldwide. We provide commissioning, qualification…
Experience: 3 to 5 years QP experience
Type: Full-time
Benefits: Hands on certifications and professional training, collaborative culture

Jabil

Project Manager, Medical Device Bray
Skills & Focus: Project Management, Medical Devices, Leadership, Financial Management, Project Planning, Customer Collaboration, Risk Analysis, KPI Management, Continuous Improvement, Team Building
About the Company: Jabil is a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of exp…
Experience: Minimum 5 years of project management experience in regulated industries (preferably in medical production).
Type: Full time
Project Engineer (Packaging) Bray
Skills & Focus: automation, packaging, medical devices, manufacturing, cross-functional teams, project management, optimization, continuous improvement, statistical analysis, regulatory compliance
About the Company: At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive eng…
Experience: 4+ years’ experience in a manufacturing environment with high-volume automated assembly and packaging experience is preferable.
Type: Full time
Lead Mechanical Design Engineer Bray
Skills & Focus: design, development, verification, medical devices, manufacturability, cross-functional teams, risk assessment, quality improvement, root cause analysis, regulatory compliance
About the Company: Jabil combines global reach with local expertise to deliver scalable and customized engineering, manufacturing, and supply chain solutions.
Experience: Minimum 6-9 years design engineering experience in medical device design
Type: Full time