117 Manufacturing jobs in Ireland

**Who we want**
+ **Performance** : Deliver high quality products.
+ **Team Player** : Build positive relationships with others to achieve common goals.
+ **Reliable** : Manage time to effectively get the job done.
A Manufacturing Operator effectively builds the products manufactured by Stryker to the required quality standard
**What you will do**
+ Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards
+ Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost
+ Monitor and verify quality in accordance with workmanship standards and operating procedures
+ Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements
+ Provide cross training to other employees
+ Contribute as part of a team in achieving the line core metrics
+ Build Quality into all aspects of their work by maintaining compliance to all quality requirements
**What you need**
+ Leaving Certificate, Trade or equivalent education level is required
+ Previous experience in production/ assembly roles is desirable
+ Basic mathematics and good English skills
+ Good communication skills
+ Willingness to work in a team and promote teamwork
+ Previous experience in production/ assembly roles is an advantage
+ The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE)
*** Please note this is initially a 12 month fixed term contract based in our Model Farm Road location**
#IJ
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Shift - This role is for the Weekend shift. Working hours are 7am - 7pm, Friday, Saturday and Sunday.**
**Who we want**
+ **Performance** : Deliver high quality products.
+ **Team Player** : Build positive relationships with others to achieve common goals.
+ **Reliable** : Manage time to effectively get the job done.
A Manufacturing Operator effectively builds the products manufactured by Stryker to the required quality standard
**What you will do**
+ Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards
+ Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost
+ Monitor and verify quality in accordance with workmanship standards and operating procedures
+ Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements
+ Provide cross training to other employees
+ Contribute as part of a team in achieving the line core metrics
+ Build Quality into all aspects of their work by maintaining compliance to all quality requirements
**What you need**
+ Leaving Certificate, Trade or equivalent education level is required
+ Previous experience in production/ assembly roles is desirable
+ Basic mathematics and good English skills
+ Good communication skills
+ Willingness to work in a team and promote teamwork
+ Previous experience in production/ assembly roles is an advantage
+ The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE)
*** Please note this is initially a 12 month fixed term contract based in our Model Farm Road location**
#IJ
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Who we are:**
Abbott has a presence in over 160 countries and has over 113,000 employees. Our new manufacturing facility in Kilkenny (R95 A02A) is Abbott's 7th manufacturing site in Ireland.
The facility is a centre for world-class engineering, quality, medical device manufacturing. We have been making a difference in the lives of Irish people since 1946.
**Abbott Ireland**
In Ireland, Abbott employs around 6,000 people across ten sites. We currently have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford, Kilkenny and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**What is this position:**
As Manufacturing Technician you will provide technical support relating to equipment utilized in the manufacturing areas by repairing, maintaining, or modifying production equipment.
Monitoring machine output on the shift to and ensure all cells are running to cycle time, to meet specific targets.
**What You'll Be Doing:**
+ Install and equipment validation
+ Conducting scheduled maintenance, diagnosing, and troubleshooting faults
+ Perform skilled maintenance and repair such as mechanical, pneumatics, electrical systems
+ Lead on maintenance and/or process issues
+ Ability to interpret blueprints and schematics.
+ Certifies and train manufacturing associates in the production processes.
+ Identifies and implements corrective actions for manufacturing related issues.
**How does this role fit into the organisation:**
You will report to a process Engineering Manager on a team of approx. 20. Your team will include process engineers and manufacturing technicians.
**What we're looking for:**
+ Min level 6 qualification (Trade or Third level equivalent)
+ Electrical and mechanical skills are desired
+ Technical and fault-finding skills
**What's in it for you:**
+ Pension
+ Healthcare
+ Bonus
+ Life insurance
+ Disability insurance
+ Paid maternity leave
+ Parental leave
+ Adoptive leave
+ Flexible working
Connect with us at or , on LinkedIn at , on Facebook at and on Twitter @AbbottNews.
Abbott is an equal opportunities employer
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

**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
Connect with us at and on LinkedIn , Facebook , Instagram , X and YouTube .
**Purpose Statement**
Provides support to the manufacturing organisation to facilitate efficient operations within the production area, to optimise existing processes, and to ensure that production goals are met. Monitors performance of equipment, machines and tools and corrects equipment problems or process parameters that produce non- conforming products, low yields or product quality issues.
Interfaces with research and development organisations to integrate
new products or processes into the existing manufacturing area.
**Key Responsibilities:**
+ Implements a staffing plan by identifying resource requirements, writing justifications for additional personnel, obtaining approval for changes, and coordinating the selection process with Human Resources (HR).
+ Develops direct reports (if applicable) by securing appropriate training, assigning progressively challenging tasks, applying progressive disciplinary action as appropriate and conducting formal written and verbal performance reviews.
+ Monitors daily work operations and provides direction and guidance to lower-level supervisors, experienced exempt employees, or skilled non-exempt staff to achieve unit or project goals.
+ Interacts with internal and external customers, by meeting regularly, responding to requests and explaining procedures.
+ Interprets and executes policies that affect work processes and personnel within the assigned organisational unit.
+ Contributes to the development of operational policies and procedures that affect personnel within the assigned organisational unit.
+ Monitors compliance with company policies and procedures (for example (e.g.) compliance with Food and Drug Administration (FDA), British Standards Institution (BSI) , Equal Employment Opportunities regulations etcetera (etc.)).
+ Monitors internal and external indicators by reviewing reports and newsletters, reading organisational literature, meeting with peers and reading departmental reports.
+ Contributes to the development and monitoring of area budget through regular analysis of cost and spending.
+ Participates in validation activity. Role may vary between providing input to owning activities such as protocol/report writing and managing execution of validation activities.
**Education and Job Skills:**
1. (Experience/Education) National Framework of Qualifications (NFQ) level 7 qualification in a relevant discipline and 6+ years of related work experience or an equivalent combination of education and work experience.
2. (Technical/Business Knowledge (Job Skills)) Monitors progress of exempt individua ls, team s, supervisors or non-exempt technical individuals toward departmental goals; monitors costs of projects and of human and material
resources within a department or unit; monitors external environment in area of technical or professional responsibility. Will perform this job in a quality system
environment. Failure to adequately perform tasks can result
in noncompliance with governmental regulations.
3. (Cognitive Skills) Develops and/or identifies new work processes and the improved utilisation of human and material resources within the assigned area or related departments; facilitate s others involvement in the continuous improvement programme; investigates and solves problems that impact work processes and personnel within the assigned unit.
4. (Influence/Leadership) Promotes the attainment of group goals by selecting, motivating , and training capable staff. Provides leadership to assigned units by communicating and providing guidance towards achieving group objectives.
5. (Planning/Organisation) Schedules human and material resources within a group or section in conjunction with near-term plans to ensure their availability ; carries out operations within an established budget.
6. (Decision Making/Impact) Assignments are expressed in the form of tasks and objectives; generally makes day-to-day decisions within established guidelines regarding work processes or schedules in order to achieve the programme
objectives established by senior management; consequences of erroneous decisions would normally result in serious delays to assigned projects or operations with substantial expenditure human resources, and funds, without jeopardising future business activity.
7. (Supervision Received) Works under minimal supervision. Independently determines and develops approach to solutions. Work is reviewed upon completion for adequacy in meeting objectives.
8. (Supervision Provided) Provides direction and guidance to supervisors, experienced exempt and/or skilled non-exempt levels of employees; evaluates performance of and assists in career development planning for subordinates; often responsible for a local functional or process activity.
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

?05 - Operations Engineering Support 2
Req ID: 122868
Remote Position: No
Hiring Manager: Caroline Scully
Band: 05
Region: Europe
Country: Ireland
State/Province: Galway
City: Galway
**General Overview**
**Functional Area:** ENG - Engineering
**Career Stream:** OPE - Operations Engineering
**Role:** Technical Support 2
**SAP Short Name:** TS2
**Job Title:** Operations Engineering Support 2
**Job Code:** TS2-ENG-OPS
**Job Level:** Band 05
**Direct/Indirect Indicator:** Direct
**Summary**
The Equipment Maintenance Technician is responsible for the set-up, installation, maintenance and support of automated equipment ensuring optimum performance and the achievement of operational goals. The Equipment Maintenance Technician works closely with teams to resolve manufacturing issues and constraints while implementing safe and robust solutions to improve overall efficiency through improvement projects around run rate increase, cycle time gains, yields and quality.
This position for the day 8 AM - 8 PM Days.
This position will report to the Team Leader.
**Detailed Description**
- Repairs and troubleshoots electro/mechanical equipment failures.
- Schedules and performs preventative maintenance procedures.
- Helps move, install, set-up and refurbish equipment.
- Maintains accurate and up-to-date maintenance documentation.
- Records significant downtime issues and resolutions in appropriate databases.
- Interacts with other departments as required to co-ordinate equipment repairs.
- Works proactively to ensure performance targets are met; Yield/quality (using SPC/SQC)/production outs/up-time /process stability.
- Communicates potential problems that may affect capacity and quality to the Business Unit Team Leader as well as across zones/work areas where necessary.
- Attends pass-downs as required and provides status updates.
- Provides detailed inputs into failed spare parts management process.
- Supports Process Engineers to ensure Continuous Improvements are ongoing.
- Trains and assists other Technicians and Operators.
**Knowledge/Skills/Competencies**
+ Strong knowledge of the setup, operation, and maintenance of specific equipment sets used in manufacturing processes.
+ Strong troubleshooting/Problem solving skills.
+ Demonstrates a high level of technical ability, with hands on approach to solving technical issues.
+ Excellent written and verbal communication skills.
+ Good interpersonal skills and ability to work as part of a team.
+ Commitment to achievement of manufacturing excellence.
+ High level of flexibility: shift changes / training courses / preventative maintenance and Project support.
+ Ability to work on own initiative, is self-driven.
+ Resourceful, hands-on, enjoys a challenge.
+ Works well under pressure.
**Typical Experience**
- 2 - 4 years+ experience as a Technician in a high volume automated environment.
- Minimum Cert./Diploma/Senior Trades in Electrical/Mechanical Engineering or equivalent.
- Working knowledge of PLCs, Motor drives, pneumatic and hydraulic components is an advantage.
Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

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
AbbVie helps people around the world live better days and better lives each year. And that takes all of us.
We are now recruiting for a Manufacturing Analyst to join our newly formed Central Cervices Team in AbbVie Westport, Co Mayo on an initial 12 months fixed term contract.
Established in 1977, AbbVie Westport is a Centre of Excellence for Aseptic for Commercial manufacturing of Biologics & Eyecare (pharmaceutical) products. In this role you will be actively involved and manage the batch related CAPA's as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigations are complete in a timely manner.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:
Key activities:
+ Use and maintenance of data within key systems such as SAP, S4HANA, Global Trackwise, POMs, One Track, One Vault and Compliance wire.
+ Document retrieval from local files and archives, as required for submissions, customer requests and others.
+ Tracking and Analysis of EM trends within the Eyecare Business Unit
+ Management of training curriculum for all using eLMS
+ Participate in and lead non-conformance and exception investigations as necessary.
+ Complete manufacturing investigations for LIRs.
+ Open and lead change control records using One Track.
+ Work with QA Teams to align and promote awareness on data integrity and good documentation practices.
+ Provide assistance when required at Regulatory Inspections.
+ Trending and co-ordination of customer complaints investigations.
+ Work close with Depts on corrective actions arising from Environmental excursions.
+ Comply with AbbVie policies and procedures and regulatory agency regulations.
Qualifications
Education and preferred experience:
+ Bachelor's degree in science, or a related field is preferred and/or a minimum of 2 years' experience in a similar role.
+ Detailed knowledge of CGMP and aseptic practices, data integrity requirements and GDP is required for this role.
+ Strong organizational skills and attention to detail are essential for this role.
+ Good interpersonal relations/communications skills
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:

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
There are many ways to be a difference maker. Find yours.
We are now recruiting for Manufacturing Technicians to join our diverse Biologics team in Westport, on an initial 12 months fixed-term contract basis. As our newest technician, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding, filling and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring.
PLEASE NOTE: The following role is a 12 hour monthly rotational shift pattern, covering days, nights, weekdays and weekends.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more.
Your Key Activities will include, but are not limited to:
+ Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
+ Perform activities associated with the compounding, filling and capping of an aseptic process.
+ Prepare components and equipment for processing into a Grade A environment.
+ Accurately completing documentation on time, accurately and legibly.
+ Keeping the Manufacturing area tidy and clean.
+ Review and update documentation as requested by the Production Manager
+ Participating in root cause analysis and problem-solving.
+ Completing compliant investigations and environmental excursions.
+ Adhering to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.
+ Follow gowning procedures on entry to areas
+ Report any machine issues to the Production Manager and the maintenance department.
+ Set-up, clean and maintain equipment
+ Transfer of waste material out of the cleanroom areas
+ Perform environmental monitoring
+ Participate in media runs
+ Adhere to and support all EHS & E standards, procedures, and policies.
Qualifications
Education and Experience:
+ Leaving cert or equivalent qualification required, 3rd level qualification in a Science/Engineering or related discipline is preferred
+ 1-2 years GMP experience, preferably Aseptic/Sterile Manufacturing in a cleanroom environment
+ Experience working with SAP within a similar industry is preferable.
+ Strong communication, documentation, and IT skills.
+ Ability to multitask and adapt in a fast-paced environment.
+ Outstanding organization, flexibility, and time management skills
+ High attention to detail and methodical in approach
+ Ability to build strong relationships and work within cross-functional teams.
+ Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
+ Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
+ Team player who can collaborate with others to achieve organizational targets and goals.
So, does this all sound like the right role for you?
Then apply now and join AbbVie today!
#Monster
Additional Information
Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) - a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.
At AbbVie, your individual contributions count - help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV - we will discuss everything else with you in person.
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:

05 - Operations Engineering Support 2 Req ID: 122868 Remote Position: No Hiring Manager: Caroline Scully Band: 05 Region: Europe Country: Ireland State/Province: Galway City: Galway General Overview Functional Area: ENG - Engineering Career Stream: OPE - Operations Engineering Role: Technical Support 2 SAP Short Name: TS2 Job Title: Operations Engineering Support 2 Job Code: TS2-ENG-OPS Job Level: Band 05 Direct/Indirect Indicator: Direct Summary The Equipment Maintenance Technician is responsible for the set-up, installation, maintenance and support of automated equipment ensuring optimum performance and the achievement of operational goals. The Equipment Maintenance Technician works closely with teams to resolve manufacturing issues and constraints while implementing safe and robust solutions to improve overall efficiency through improvement projects around run rate increase, cycle time gains, yields and quality. This position for the day 8 AM - 8 PM Days. This position will report to the Team Leader. Detailed Description Repairs and troubleshoots electro/mechanical equipment failures. Schedules and performs preventative maintenance procedures. Helps move, install, set-up and refurbish equipment. Maintains accurate and up-to-date maintenance documentation. Records significant downtime issues and resolutions in appropriate databases. Interacts with other departments as required to co-ordinate equipment repairs. Works proactively to ensure performance targets are met; Yield/quality (using SPC/SQC)/production outs/up-time /process stability. Communicates potential problems that may affect capacity and quality to the Business Unit Team Leader as well as across zones/work areas where necessary. Attends pass-downs as required and provides status updates. Provides detailed inputs into failed spare parts management process. Supports Process Engineers to ensure Continuous Improvements are ongoing. Trains and assists other Technicians and Operators. Knowledge/Skills/Competencies Strong knowledge of the setup, operation, and maintenance of specific equipment sets used in manufacturing processes. Strong troubleshooting/Problem solving skills. Demonstrates a high level of technical ability, with hands on approach to solving technical issues. Excellent written and verbal communication skills. Good interpersonal skills and ability to work as part of a team. Commitment to achievement of manufacturing excellence. High level of flexibility: shift changes / training courses / preventative maintenance and Project support. Ability to work on own initiative, is self-driven. Resourceful, hands-on, enjoys a challenge. Works well under pressure. Typical Experience 2 - 4 years+ experience as a Technician in a high volume automated environment. Minimum Cert./Diploma/Senior Trades in Electrical/Mechanical Engineering or equivalent. Working knowledge of PLCs, Motor drives, pneumatic and hydraulic components is an advantage. Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law). At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them. To Apply Please forward your CV via the APPLY Now button below.

Manufacturing Engineer - County Clare. Job Duties: Providing Manufacturing Engineering support to both customers and suppliers Providing support to the Production Team in terms of planning and designing new processes in a manner that can be easily implemented Manufacturing of prototypes and validation of product within specification with a view to upscaling to full product runs Identifying and implementing improvements to equipment, processes and methods Identifying and driving improvement initiatives to reduce costs and improve on-time delivery Responsible for applying, maintaining and improving lean manufacturing procedures Playing a role in developing processes and implementation of a new ERP system Actively supporting the Engineering team to ensure task flexibility Ensure proper documentation of technical data generated for the assigned projects and/or tasks is consistent with engineering policies and procedures Make recommendations concerning the development of new products or services that will enhance the product offering to customers Requirements and Skills sought for this position: Bachelors degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or related field. Lean Six Sigma certification or training (Green Belt or higher) is advantageous, although not essential. Knowledge of ERP systems. At least 25 years' experience in a manufacturing or industrial engineering role. Proven experience with process development, optimisation, and improvement initiatives. Experience in prototype manufacturing, testing, and validation. Hands-on experience with lean manufacturing principles and continuous improvement projects. Experience in equipment set-up, troubleshooting, and production support. Strong knowledge of manufacturing processes, tools, and methods. Proficiency in CAD software (e.g. SolidWorks, AutoCAD) for process or tooling design. Understanding of quality control methods and statistical analysis tools. Familiarity with root cause analysis (RCA), FMEA, and corrective/preventive actions (CAPA). Knowledge of safety standards and regulatory requirements in manufacturing. Ability to collaborate cross-functionally with production, quality, and supply chain teams. Excellent communication and documentation skills. Adaptability to support multiple tasks and projects simultaneously. Continuous improvement mindset with initiative to identify and implement changes. Skills: manufacturing engineer cnc sheetmetal sheet metal sheet-metal fabrication machining