373 Manufacturing Processes jobs in Ireland

About Analog Devices
Analog Devices, Inc. (NASDAQ: ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancements in digitized factories, mobility, and digital healthcare, combat climate change, and reliably connect humans and the world. With revenue of more than $9 billion in FY24 and approximately 24,000 people globally, ADI ensures today's innovators stay Ahead of What's Possible. Learn more at and on LinkedIn and Twitter (X).

Analog Devices (NASDAQ: ADI) designs and manufactures semiconductor products and solutions. We enable our customers to interpret the world around us by intelligently bridging the physical and digital worlds with unmatched technologies that sense, measure and connect.

We are looking for an experienced industrial/manufacturing engineer with exposure to working in a complex multi-process environment to join our team in Limerick.

The successful candidate will be a part of the Limerick Operations and Technology team working in our best-in-class wafer manufacturing clean-rooms. The role involves working with our Engineering and Operations teams to improve complex wafer level processes and systems, and to identify opportunities for productivity improvements. This is an opportunity to work in a dynamic work environment while interacting with Operations and Engineering teams from multidisciplinary backgrounds.

Responsibilities/Duties

• Analysing operations and processes to maximize productivity.
• Develop and enhance capacity and headcount models for operations.
• Develop an Overall Manufacturing Efficiency model for roll out in production with focus on SEMI-E10 and SEMI-E79 requirements.
• Identify capacity limitations in a complex multi processes cleanroom.
• Designing production processes that maximize efficiency and reduce waste.
• Designing control systems to minimize cost and production issues.
• Develop production standards across operations.
• Mapping of inventory flow & optimizing flow / pull within and between manufacturing cells.
• Design of manufacturing layouts for efficiency
• Application of Visual factory concepts

The Candidate:

The ideal candidate must be self-motivated, dynamic, meticulous, proactive, prepared to take the initiative, drive change, and exhibit the following skills:

• Honours Degree in industrial engineering or related field required.
• Advanced knowledge of production machinery, processes, and standards, semiconductor manufacturing experience an advantage.
• Critical thinking and problem-solving skills.
• Troubleshooting skills and attention to detail.
• Documentation and organization skills.
• Excellent verbal and written communication skills
• Quick learning capability.
• Strong sense of work ethics.
• Excellent interpersonal and influencing skills.
• Minimum of 2 years work experience in a related field

For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls. As such, applicants for this position – except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. 1324b(a)(3) – may have to go through an export licensing review process.
Analog Devices is an equal opportunity employer. We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, parental status, disability, medical condition, genetic information, military or veteran status, union membership, and political affiliation, or any other legally protected group.
Job Req Type: Experienced

Required Travel: Yes, 10% of the time

Shift Type: 1st Shift/Days

About Analog Devices
Analog Devices, Inc. (NASDAQ: ADI ) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancements in digitized factories, mobility, and digital healthcare, combat climate change, and reliably connect humans and the world. With revenue of more than $9 billion in FY24 and approximately 24,000 people globally, ADI ensures today's innovators stay Ahead of What's Possible. Learn more at and on LinkedIn and Twitter (X).

Industrial/Manufacturing Engineer
Job location
: Limerick, Ireland

Analog Devices (NASDAQ: ADI) designs and manufactures semiconductor products and solutions. We enable our customers to interpret the world around us by intelligently bridging the physical and digital worlds with unmatched technologies that sense, measure and connect.

We are looking for an experienced industrial/manufacturing engineer with exposure to working in a complex multi-process environment to join our team in Limerick. The ideal candidate will need excellent attention to detail to analyze, interpret and monitor our current operations and determine opportunities for improvement and implementation of same.

The industrial engineer's responsibilities include analyzing operations, designing workflows and production processes, reducing inefficiency, and ensuring that final products meet the established quality standards. A record to show productivity improvements and ability to drive change and deliver results across multiple groups is necessary.

The successful candidate will be a part of the Limerick Operations and Technology team working in our best-in-class wafer manufacturing clean-rooms. The role involves working with our Engineering and Operations teams to improve complex wafer level processes and systems, and to identify opportunities for productivity improvements. This is an opportunity to work in a dynamic work environment while interacting with Operations and Engineering teams from multidisciplinary backgrounds.

Responsibilities/Duties

• Analysing operations and processes to maximize productivity
• Develop and enhance capacity and headcount models for operations
• Develop an Overall Manufacturing Efficiency model for roll out in production with focus on SEMI-E10 and SEMI-E79 requirements
• Identify capacity limitations in a complex multi processes cleanroom
• Designing production processes that maximize efficiency and reduce waste
• Designing control systems to minimize cost and production issues
• Develop production standards across operations
• Mapping of inventory flow & optimizing flow / pull within and between manufacturing cells
• Design of manufacturing layouts for efficiency
• Application of Visual factory concepts

The Candidate:

The ideal candidate must be self-motivated, dynamic, meticulous, proactive, prepared to take the initiative, drive change, and exhibit the following skills:

• Honors Degree in industrial engineering or related field required.
• Advanced knowledge of production machinery, processes, and standards, semiconductor manufacturing experience an advantage.
• Critical thinking and problem-solving skills.
• Troubleshooting skills and attention to detail.
• Documentation and organization skills.
• Excellent verbal and written communication skills
• Quick learning capability.
• Strong sense of work ethics.
• Excellent interpersonal and influencing skills

For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls. As such, applicants for this position – except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. 1324b(a)(3) – may have to go through an export licensing review process.
Analog Devices is an equal opportunity employer. We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, parental status, disability, medical condition, genetic information, military or veteran status, union membership, and political affiliation, or any other legally protected group.
Job Req Type: Experienced

Required Travel: No

Shift Type: 1st Shift/Days

We are looking for a dedicated Administrator who would be a key member of the company leadership team, responsible for ensuring that the service we provide is safe and compliant with all industry and certification regulations.

The candidate should have a "can-do" attitude that drives effective change and moves the company processes positively which will effectively lead to the provision of an optimum service to our clients.

We seek an effective coach and communicator who can skillfully create an empowered and engaged workforce culture.

The candidate should have knowledge of construction safety, quality and continuous improvement via effective data analysis and decision-making.

Key Responsibilities:

· Assure that all stakeholders are well trained in support of the I.M.S

· Manage and supervise I.M.S. administration and site activities

· Ongoing auditing to promote compliance with I.M.S. and H&S procedures

· Use effective negotiation skills to drive alignment and resolve conflict

· Provide coaching and constructive feedback

· Collaborate with team and cross-functional stakeholders

· Evaluate data, assess and develop ongoing improvements to the company I.M.S. and H&S procedures

Requirements:

· 3+ years of experience in quality management / Health & Safety

· Experience in business administration will be an advantage.

· In-depth knowledge of health & safety /quality control procedures and legal standards.

· Strong attention to detail, organisational, and leadership skills.

· Strong knowledge of data analysis, and statistical methods.

· Excellent communication and listening skills.

· Formal training in H&S and environmental monitoring and auditing will be an advantage

Job Types: Full-time, Permanent

Pay: €40,000.00-€50,000.00 per year

Benefits:

• Company pension
• On-site parking

Work Location: In person

Job Description
We have a great opportunity for a Quality Control Specialist to join our Carlow site. You will join a self-directed team and provide trouble shooting support. The quality control specialist will have the opportunity to be involved in and lead various exciting projects.

What you will do

Bring energy, knowledge, innovation and leadership to carry out the following

• Support new product introductions and provide quality expertise during product release.
• Generate, review, approve, and expedite QC GMP documentation, including Quality Notifications, Laboratory Investigations, CAPAs, Effectiveness Checks, SOPs, SWIs, change controls, Annual Product Reviews, Trend Reports, Out of Process Control Limit (OOPCL) events, and Compendial Assessments.
• Develop, revise, and roll out operational procedures and training materials.
• Lead and support batch release activities by completing timely investigations, quality notifications, OOPCL events, and generating interim/summary reports.
• Raise and investigate CAPAs and quality notifications using standard problem-solving tools (FMEA, Fishbone diagrams, 5 Whys), and implement corrective actions via change management.
• Provide coaching, mentoring, and guidance to lab teams
• Act as a document system expert review, approve, format, and facilitate documentation workflows.
• Lead or support projects and promote teamwork, open communication, and a high-performing, inclusive culture.
• Collaborate cross-functionally to ensure manufacturing, testing, and release processes comply with cGMP and regulatory standards.
• Support qualification/validation, technical transfers, and commercial operations with quality oversight.
• Perform laboratory testing and material inspections according to approved methods, including analytical, microbiological, environmental monitoring, and stability testing.
• Detect, report, investigate, and close out out-of-specification (OOS) and out-of-trend (OOT) results.
• Manage and monitor Quality Management Systems, generate performance and quality event reports.
• Provide quality support for supplier/material qualification, validation, risk management, and quality agreements.

Lab operates on a two-shift cycle pattern (7am-3pm/3pm-11pm)
In order to excel in this role, you will more than likely have

• Bachelor's degree or higher in Analytical Chemistry, Biochemistry, Biology, or a related discipline preferred.
• 5+ years' experience in a pharmaceutical laboratory, ideally in a similar role.
• Excellent troubleshooting, analytical, and problem-solving skills.
• Strong technical knowledge and scientific qualification relevant to the pharmaceutical environment.
• Strong experience with HPLC systems, bioassay methods, and associated software is desirable.
• Experience with cGMP, GLP, Quality Management Systems, method validation, and method transfer.
• Proficient in QC systems such as EN, LIMS, Trackwise, and Microsoft Office.
• Knowledge of Irish, European, and international regulatory codes and standards.
• Effective verbal and written communication skills with strong influencing capability.
• Commitment to maintaining a safe, compliant, and quality-focused culture.

As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.

So, if you are ready to
Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world's leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.

Required Skills
Accountability, Accountability, Adaptability, Analytical Chemistry, Analytical Instrumentation, Analytical Method Development, Batch Releases, Biochemistry, Corrective Action Management, Data Integrity, Dissolution Testing, Driving Continuous Improvement, GMP Compliance, Ishikawa Diagrams, Karl Fischer Titrations, Laboratory Documentation, Laboratory Safety, Laboratory Testing, Management Process, Microbiological Analysis, Microbiological Test, Microsoft Office, Quality Control Management, Quality Management System Auditing, Quality Management System Improvement {+ 4 more}

Preferred Skills
Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status
Regular

Relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Not Applicable

Shift
Valid Driving License
Hazardous Material(s)
Job Posting End Date
10/17/2025

• A job posting is effective until PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID
R

Overview:

The Engineer is responsible for setting out the site and applying dimensional controls in line with drawings, specifications and surveys. The role ensures that tolerances are met without loss of quality or space and supports efficient sequencing of works. The Engineer provides technical advice, monitors quality and assists the project team in line with company procedures and the Sisk Safety Statement.

John Sisk & Son have been building excellence as a family-owned international construction company by offering trust, certainty and value to our clients whilst being at the heart of change.

Responsibilities:

• Set out works in line with drawings, specifications and site surveys
• Liaise with planners to align programmes and supplier outputs
• Check materials and works in progress for compliance with specifications and quality standards
• Contribute to Inspection and Test Plans and ensure supply chain provides required test data
• Raise and resolve RFIs with client representatives, suppliers, subcontractors and statutory bodies
• Maintain quality control and records in line with method statements, quality plans and inspection procedures

• Review subcontractor drawings and ensure correct use of contract records and specifications

• Ensure purchase orders define technical requirements accurately

• Strong interpersonal and communication skills with ability to influence and work with senior management
• Ability to analyse, evaluate and adapt approach to project needs
• Experience across a range of trades including piling, geotechnical, substructures, superstructures and facades
• Competence in BIM and ability to work with 3D scanning or point cloud data an advantage
• Articulate and numerate with ability to produce objective and persuasive reports
• Demonstrates initiative, resilience and problem-solving ability

Experience:

• Experienced Engineer able to direct a team, and others that do not report directly.
• Have a good knowledge of construction processes and standards.
• Computer literate.
• Must be able to evaluate information to assess compliance with requirements and identify improvement opportunities. This should include the ability to analysis data to identify trends.
• Organisational skills and workload prioritising.
• Good interpersonal skills
• Ability to work independently and use initiative.
• Ability to work as part of a team.
• A commitment to identify, develop, direct and implement key objectives
• Able to deal with staff, clients, and external customers.
• Supervise and mentor junior or trainee engineers
• Provide input into measurement and valuation with the project quantity surveyor
• Maintain site diaries and prepare reports
• Carry out pre-start condition surveys
• Manage and record delivered materials including concrete, reinforcement and structural products
• Assist with installation of site facilities such as hoardings and accommodation
• Carry out snagging and de-snagging before handover
• Support safe working practices including reviewing subcontractor safety plans and preparing method statements
• Actively develop own skills and mentor others through knowledge sharing

Qualifications:

Required

• Degree or Diploma in Engineering
• SMSTS or MSIC certification
• First Aid training
• Lifting Supervisor certification
• Temporary Works Coordinator training
• Chartered or working towards professional membership with Engineers Ireland or the Institution of Civil Engineers

Desirable

• Project Management qualification
• Training in planning software
• Current full driving licence

Additional Information:

• Competitive Salary with yearly increase
• 26 days holiday (option to purchase 5 more)
• Company Car or Car allowance
• Employer pension
• Competitive mileage rate
• Travel expenses
• Flexible and remote working
• Enhanced parental leave
• Professional and Educational development

Our people are at the heart of our success and our proposition to them is work with purpose, have time for life, build a career with no limits and surround yourself with great people.

Our Internal Recruitment Team fulfil all vacancies on a direct basis. Unsolicited contact by unapproved agencies (sharing speculative CVs) will not be accepted and introductory fees will not apply.

Sisk Group is an equal opportunities employer. We welcome applications from all qualified candidates, regardless of gender, race, ethnicity, disability, age, sexual orientation, religion, or any other protected characteristic. We are committed to fostering an inclusive workplace and will provide reasonable adjustments during the recruitment process where required.

This role profile and all associated recruitment materials have been prepared in line with current and emerging legal and regulatory requirements, including the EU Pay Transparency Directive and the Equality Acts (UK & Ireland). All language is gender-neutral and inclusive, and the requirements listed are based solely on objective role performance needs. Sisk Group is committed to ensuring fairness, transparency, and compliance in all recruitment and employment practices.

At Sisk we are committed to attracting and hiring diverse talent into our organisation. We know the confidence gap and imposter phenomenon can get in the way of meeting remarkable candidates. We also know that candidates from underrepresented backgrounds often don't apply for roles if they don't feel they meet all the criteria. Give your transferable skills the chance to tell the full story. It's not all about your technical expertise. Don't hold back, we'd love to hear from you.

Cairn has a unique opportunity for a Quality Manager who will play a key role within the Quality team reporting directly to the Quality Lead. They will liaise with their respective site, quality teams to advocate, promote and ensure that Quality is embedded across all sites.

Responsibilities:

• Support Quality lead with assigned certifier and Industry quality knowledge
• Coordinate, prepare and Lead in the Rollout of Procore Quality DMS platform
• Coordination of updates on Current DMS systems Quality forms and processes, with regular meetings with DMS team
• Undertake Regular reviews of Carin Quality Processes and Procedures in particular.
• Robust Benchmarking processes
• Alignment of Quality processes with current and future BCAR requirements
• Compliance with Partner/ client requirements including contractual obligations
• Review of comparable industry processes
• Attend Benchmarking inspections on site
• Independent Inhouse audit of current projects
• Product compatibility
• Product Applications and Suitability
• Product Robustness
• Identifying and issuing Quality memos and alerts as agreed with the Quality Lead
• Coordinate with Technical managers
• specifying correct products / performance criteria
• Tech Sub Approvals
• Forward look towards Homebond / LDI / Passive House / Purchaser requirements and business protection
• Undertake a schedule of inhouse training to Technical, Construction, Operational, Customer and Aftercare departments, including;
• BCAR Processes and awareness
• Facades and Fire Safety
• Assigned Certifier awareness
• Quality Management during Construction
• Identifying strategic training requirements
• Co-ordinate the implementation of project quality processes and procedures with our project teams.
• Undertake reviews of our Integrated Management system against our quality policies and procedures to ensure conformity, work with quality lead on IMS improvements in line with business requirements

The Candidate;

• 10+ years' experience in a construction/ technical or quality role
• Previous technical experience in building surveying / inspection / engineering of quality standards
• Understanding of compliance and implementation of BCAR process
• Ability to evaluate and manipulate data
• Understanding of various material compliance and compatibility
• People management & stakeholder management exp
• Curious tenacity towards problem solving with a result-oriented mindset
• Ability to develop collaborative relationships with stakeholders internally and externally
• Takes accountability to challenge, question and drive toward resolution
• Clear verbal and written communication essential

Working with Cairn:

At Cairn, we believe it is essential that our employees feel valued and appreciated. We therefore offer above industry average remuneration packages with a comprehensive benefits portfolio that's ready to support you for whatever life brings.

We are delighted to offer a suite of benefits when you join Cairn which include;

• Competitive salary
• Performance related bonus
• Pension scheme with matching contributions
• Full health insurance with Irish Life health
• Annual salary review
• Continuous Professional development (CPD) programme & funding
• Paid maternity & paternity leave
• Free Cairn annual leave days
• Life assurance
• Income protection
• Employee Assistance Programme with VHI
• Tax saver - travel and bike to work
• Culture Committee
• Talent Development Programmes
• Approved Profit Sharing Scheme (APSS)
• Company vehicle (role dependent)

The Cairn purpose is to build sustainable communities where people can thrive.

At Cairn, it's not what we build, it's why we build. It's about putting down a marker that will stand for generations to come. Creating new communities of connection and belonging for an Ireland where people can thrive. Reshaping, redefining, reinvigorating our place in the world. Building for people, progress, and potential.

Because when Cairn build, it's Built For Good.

My client is seeking to recruit a QC Material Management Analyst to join the QC Site Operations team at their Multi-Product Cell Culture Drug Substance Facility in Dublin.

Reporting to the QC Material Management Supervisor, you will be responsible for supporting site activities related to performing testing of Raw Materials, in-process samples, and laboratory duties in accordance with cGMP regulations.

Key responsibilities include:

• Performing QC testing (TOC, pH Conductivity) of water samples, and analysis of Raw Materials including HPLC, KF, UV, IR, and wet chemistry techniques. Completing laboratory documentation in a timely and accurate manner as directed.
• Ensuring compliance with Standard Operating Procedures and Registered Specifications.
• Assisting in authoring and reviewing documentation, including SOPs, as required.
• Reviewing batch paperwork and reconciling analyses performed in the laboratory, ensuring any out-of-specification results are investigated according to procedures.
• Supporting technical transfer of new projects.
• Assisting with out-of-specification investigations and deviations using the Infinity system.
• Performing sample management activities and ensuring chain of custody is maintained using CIMS and LIMS.
• Keeping up to date with current industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
• Carrying out other activities as indicated by the Lab Supervisor.

Requirements:

• Third level qualification (Degree) in Chemistry, Biology, or related discipline.
• At least 2-3 years of experience in a pharmaceutical or healthcare laboratory or related technical function.
• Strong written and verbal communication skills, with the ability to work effectively in a collaborative team environment.

The Next Step for you:

Should this position be of interest to you please submit your CV to Barry O'Mahony from Next Generation Recruitment using the apply button.

Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website. If you require any reasonable accommodations during the recruitment process please let us know and we will do our best to support you.

PE Global is currently recruiting for a Senior QC Analyst for a leading multi-national Medical Devices client based in Galway.

This is a contract position.

Role:

• Act as Subject matter expert and provide oversight for critical NPD areas:
• Dissolution/Elution (USP APPII/USP APPVII)
• Liquid/Gas Chromatography
• Analytical test method development
• Analytical test method validation
• Work independently to plan and schedule activities to meet project timelines
• · Author technical reports and validation documents
• · Provide guidance and communicate updates to cross-functional and cross-site teams
• · Support laboratory investigations to determine root cause and implement meaningful corrective actions
• · Drive continuous improvement projects to reduce testing lead-times and support cost saving targets
• · Supports Training of new colleagues
• · Supports Internal and External Audit programs
• Support Regulatory submissions

Requirements

• Bachelors degree in a science discipline

• 3-5 years experience in Medical Devices or related Industry

Interested candidates should submit an updated CV.

Please click the link below to apply, or alternatively send an up to date CV to

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

Are you passionate about microbiology and quality control in a fast-paced pharmaceutical environment?

We're looking for a
QC Microbiology Analyst
to join our Client on there site in Blanchardstown, Dublin. This is a
lab-based role
, offering the chance to make a real impact on patient safety and product quality.

About the Role

As a QC Microbiology Analyst, you'll play a vital role in ensuring our products meet the highest regulatory and quality standards. You'll carry out microbiological testing, support manufacturing operations, and contribute to continuous improvement initiatives across the site.

Key responsibilities include:

• Performing microbiological testing such as:
• Environmental monitoring
• Water sampling & testing
• Bioburden & endotoxin testing
• Growth promotion testing of media and diluents
• In-process testing & compendial verifications
• Data analysis, trending, and timely reporting of results
• Supporting method validation, verification, and transfer activities
• Liaising with cross-functional teams to ensure testing schedules are met
• Oversight of contract testing laboratories (sample shipping, reconciliation, trending)
• Preparing for and supporting internal and external audits (HPRA, FDA, Corporate)
• Driving safety, compliance, and continuous improvement initiatives

What We're Looking For

• Education:
  Minimum BSc in Science (or equivalent Level 7 Laboratory Apprentice qualification)
• Experience:
  At least 2 years in a QC role, ideally within pharmaceuticals
• Strong background in bioburden, endotoxin, and environmental monitoring (preferred)
• Experience with method validation/development (advantageous)
• Excellent problem-solving, decision-making, and communication skills
• Ability to work effectively in a team and manage priorities in a fast-paced environment
• Proficiency in Microsoft Office and technical documentation
• High levels of integrity, accuracy, and attention to detail