140 Manufacturing Technician jobs in Ireland
Manufacturing Technician
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Job Description
Manufacturing Technician
Reporting Structure
This person shall report to the Senior Manufacturing Engineer or designate.
Overall Job Objectives
The Manufacturing Technician supports day-to-day production by maintaining efficient and compliant operations on the manufacturing line. Key responsibilities include troubleshooting issues, performing equipment setups and maintenance, supporting process improvements, and ensuring accurate documentation in line with GMP and quality standards.
The Manufacturing Technician will work as part of a team to assist in the manufacture of innovative medical devices in accordance with the requirements of International Standards: ISO 13485, FDA 21 CFR Part 820, EU Medical Device Regulation (MDR) and the Vivasure Medical Quality Management System.
Main Duties and Responsibilities
- Provide day-to-day technical support to the manufacturing line to ensure consistent and efficient operations.
- Respond promptly and effectively to manufacturing line stoppages or anomalies to minimise production downtime.
- Troubleshoot and resolve issues related to equipment, tooling, process, or material.
- Perform manufacturing line set-ups and operate equipment, ensuring proper use and functionality.
- Carry out routine and preventative maintenance on production equipment.
- Identify and implement improvements to manufacturing processes, tools, jigs, and methods that enhance product quality, efficiency, and manufacturability.
- Support the elimination of waste and inefficiencies using Lean, Six Sigma, or other continuous improvement methodologies.
- Participate in process development activities for new and existing products.
- Assist with equipment, process and product verification and validation testing.
- Maintain accurate and complete batch records, logs, check sheets, and maintenance records in compliance with GMP and quality system requirements.
- Conduct or support in-process inspection, functional testing, and non-conformance investigations.
- Maintain technical documentation in accordance with Quality Management System requirements.
- Provide input for risk assessments, FMEAs (Failure Modes and Effects Analysis).
- Collaborate with cross-functional teams during line validations, engineering builds or product transfers. Support product builder training on processes & work instructions.
- Work as part of the core manufacturing team to support root cause analysis and implement corrective and preventive actions.
- Maintain equipment, work areas and facilities to ensure a clean and safe work environment and compliance to good manufacturing practice.
Qualification Required
- Third level qualification in a relevant technical field is advantageous.
- Knowledge of quality standards including ISO 13485, MDR, and FDA Requirements.
Work Experience or Training Required
- 2-5 years hands-on experience in
- Medical device / pharma industry
- Operating and maintaining production equipment
- Supporting process improvements
- Working knowledge of QMS and regulatory requirements in the medical device industry.
Special Skills Required
- Excellent communication and organisational skills
- Works effectively in a team environment
- Takes ownership of responsibilities and can work autonomously as required
- Good documentation practices (GDP) and strong working knowledge of Microsoft Word, Excel, Powerpoint etc.
- Knowledge of cleanroom manufacturing processes and methodologies
- Ability to read technical drawings, process diagrams, and equipment manuals.
Manufacturing Technician
Posted today
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Job Description
Requisition ID: 70680
Date: Sep 25, 2025
Location:
Dublin, Leinster, IE
Department: Engineering
Description:
At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
Job SummaryIn this role, you will be responsible for developing new technology and supporting existing technology to improve production, quality, profitability and safety. This individual will be responsible for the planning, scheduling, execution of projects and communicating project status to targeted timelines. This individual will also manage/assist in facility expansion/modifications.
We have permanent and fixed term contracts available.
Essential Duties and Responsibilities- Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety.
- Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures.
- Ensure technical and customer requirements for assigned projects are achieved.
- Develop and maintain required validation and project management documents.
- Conduct or participate in routine project reviews with Project Teams and Management
- Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts.
- Develop and/or review engineering change requests for modifications to processes, equipment and facilities.
- Troubleshoot and repair of all automation.
- Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation.
- Ensure automation lines are meeting their targeted output and OEE by analyzing production data.
- Maintain quality finished product through proper maintenance and operation of all automation.
- Provide timely notification to shift leaders and program managers of maintenance and down time issues.
- Interfaces daily with engineering manager and shift support staff.
- Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
- Performs other duties as assigned by management.
- Exhibits regular, reliable, punctual and predictable attendance.
- Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.
- Associate's Degree In a relevant Engineering subject required or
- Bachelor's Degree In a relevant Engineering subject preferred
- Minimum 3 years Experience in medical device industry or other regulated industry required
- Minimum 3 years Experience in supporting technical project management preferred
- Background in medical devices/pharmaceutical would be a plus.
- Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards
Travel Requirements
5%: Up to 13 business days per year
Physical RequirementsLight-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.
Additional Requirements- Must be able to work a 40-hour work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues.
- Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate fumes and particulate generated from various plastics. Work areas are equipped with adequate lighting, cooling/heating and equipment that are in a good working condition. Must work constructively in an environment that may always be stressful due to competing resources while maintaining company confidentiality.
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.
Manufacturing Technician
Posted today
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Job Description
About the job - Manufacturing Technician
Permanent employee, Full-time
An exciting opportunity has opened for a
Manufacturing Technician
to join a leading organisation in the
biopharmaceutical manufacturing sector
. This role is ideal for someone who wants to develop their career in a regulated GMP environment while working with innovative technologies.
Key Responsibilities
- Carry out GMP manufacturing and improvement activities to support production.
- Maintain cleanroom standards, ensuring compliance with GMP, GDP, and Data Integrity.
- Manage materials and bioprocessing activities within ERP systems.
- Support safety and quality investigations, driving continuous improvement.
- Contribute to a safe, compliant, and inspection-ready manufacturing environment.
Qualifications
- Experience in a GMP manufacturing environment (preferred but not essential).
- Strong attention to detail and adherence to cleanroom behaviours.
- Good communication skills (written and verbal).
- Comfortable working rotating shifts (early, late, and potential night shifts).
- Competency with IT systems (e.g., Microsoft Office).
What We Offer
- Permanent, full-time opportunity within advanced biopharmaceutical manufacturing.
- Structured training and career development in a regulated GMP environment.
- Exposure to innovative technologies and processes.
- Supportive team culture with a focus on safety, quality, and improvement.
- Competitive package including
shift premium
for late and night work.
Manufacturing Technician
Posted today
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Job Description
Position Title:
Manufacturing Technician
Location:
Athlone, Co. Westmeath
Key Responsibilities:
- Operate, maintain, and troubleshoot manufacturing equipment to ensure optimal performance and minimal downtime.
- Diagnose and resolve mechanical issues using problem-solving techniques to maintain production efficiency.
- Conduct routine maintenance and calibration of equipment in compliance with industry regulations.
- Ensure adherence to all safety, quality, and regulatory standards within a manufacturing environment.
- Collaborate with cross-functional teams, including engineering and quality assurance, to improve processes and equipment performance.
- Maintain accurate documentation and reports related to equipment performance, maintenance activities, and any deviations.
- Support continuous improvement initiatives and contribute to process optimization projects.
Qualifications:
- Certificate or Diploma in Mechanical Engineering or a related discipline.
- Minimum of 3 years of experience in a regulated manufacturing environment.
- Strong problem-solving skills with the ability to troubleshoot and resolve mechanical issues efficiently.
- Experience working in a GMP, ISO, or similar regulated manufacturing setting.
Preferred Qualifications:
- Experience in the medical device, or precision manufacturing industries.
- Knowledge of lean manufacturing, Six Sigma, or similar process improvement methodologies.
- Strong technical aptitude with hands-on experience in mechanical systems, automation, or CNC machinery.
- Excellent communication and teamwork skills to collaborate effectively within a multidisciplinary environment.
Job Type: Full-time
Benefits:
- Company events
- On-site parking
- Private medical insurance
Education:
- Advanced/Higher Certificate (preferred)
Experience:
- Manufacturing: 3 years (preferred)
Work authorisation:
- Ireland (required)
Work Location: In person
Manufacturing Technician
Posted today
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Job Description
05 - Operations Engineering Support 2
Req ID:
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.
Manufacturing Technician
Posted today
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Job Description
Manufacturing Technician – Abbott Kilkenny
Empowering Innovation in Medical Device Manufacturing
Abbott is a global healthcare leader operating in over 160 countries with more than 113,000 employees. In Ireland, we've been improving lives since 1946, with over 6,000 employees across ten sites — including seven cutting-edge manufacturing facilities.
Our newest site in Kilkenny is a hub of advanced engineering, precision manufacturing, and innovation. As part of our commitment to Industry 4.0, we're integrating smart technologies, data-driven decision-making, and automation to deliver world-class healthcare solutions.
About the Role
As a Manufacturing Technician, you'll be at the forefront of our smart manufacturing operations — supporting high-performance equipment, driving process excellence, and contributing to a culture of innovation. You'll join a growing, multidisciplinary team focused on delivering quality, efficiency, and continuous improvement.
What You'll Be Doing
- Install, validate, and optimize manufacturing equipment
- Perform predictive and preventive maintenance using digital tools
- Diagnose and resolve faults across mechanical, pneumatic, and electrical systems
- Lead troubleshooting and root cause analysis using data insights
- Interpret technical drawings, schematics, and digital documentation
- Train and certify operators in advanced production processes
- Identify and implement process improvements aligned with lean and Six Sigma principles
What We're Looking For
- Minimum Level 6 qualification (Trade or Third-level equivalent)
- Strong electrical and mechanical aptitude
- Proven fault-finding and problem-solving skills
- Experience with automation, sensors, or PLCs is a plus
- A proactive, detail-oriented mindset with a passion for innovation
- Ability to work independently and collaboratively in a fast-paced environment
What's in It for You
- Competitive salary and performance-based bonus
- Pension and comprehensive healthcare
- Life and disability insurance
- Paid maternity, parental, and adoptive leave
- Flexible working options
- Access to cutting-edge technologies and continuous learning
- A supportive, inclusive workplace where your ideas matter
The Right Fit
This role is ideal for someone who thrives in a technology-driven, high-performance environment. You're disciplined, dependable, and motivated by precision and progress. You bring a strong sense of ownership, a commitment to quality, and a desire to grow with a company that's shaping the future of healthcare.
Ready to power the next generation of medical manufacturing?
Apply now and be part of something extraordinary.
Manufacturing Technician
Posted today
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Job Description
Purpose of Job
The main purpose of the Manufacturing Technician is to perform manufacturing and improvement activities in accordance with Good Manufacturing Practice to support the manufacture of Advanced Therapy Medicinal Products (ATMP).
Major Activities
- Responsible for performing manufacturing and improvement activities in accordance with Good Manufacturing Practice to manufacture ATMP.
- Responsible for identifying, reporting and supporting health and safety issues and investigations, and responsible for identifying potential health and safety improvements.
- Responsible for maintaining own work and work area in an inspection-ready state at all times.
- Responsible for driving personal development, seeking opportunities to grow and expand additional capabilities.
- Responsible for communicating professionally, accurately and in a timely manner with team members and other stakeholders.
- Responsible for identifying, collaborating and delivering continuous improvements within the manufacturing area to improve safety, quality and flow.
- Responsible for identifying, reporting and supporting quality issues and investigations.
- Responsible for ensuring that individual and co-worker work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures.
- Responsible for ensuring that the necessary training is undertaken in a timely and GMP compliant manner before the task is undertaken.
- Responsible for ensuring that any GMP documentation assigned is closed in a timely manner, right-first time and in compliance with MeiraGTx procedures.
- Responsible for ensuring the facility and materials are sanitised, monitored and controlled adequately to prevent contamination or cross-contamination.
- Responsible for movement and preparation of materials required for bioprocessing and support activities inclusive of their management within the Enterprise Resource Planning system.
- Responsible for ensuring materials used within manufacturing are correct, clean, appropriate and in place ready for manufacture to the agreed schedule.
Key Performance Indicators
- Safe working of self and with others.
- Compliance with GMP requirements including Data Integrity.
- Excellent cleanroom behaviours.
- Timely closure of GMP commitments.
- High standards of professional conduct including timeliness, teamwork, respect for others, and commitment.
- All training completed prior to undertaking a task, with no overdue training.
Key Job Competencies
- Good Documentation Practice - Operates to appropriate manufacturing practices and procedures to produce and complete documentation of the highest standard.
- Cleanroom behaviours – Operates to a high standard of hygiene and technique within cleanrooms to maintain the required level of cleanliness for ATMP manufacturing.
- Motivation - demonstrates persistence and overcomes obstacles; strives for excellence and demonstrates consistent pride in own work.
- Professionalism - approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for their own actions; follows through on commitments.
- Quality Improvement - looks for ways to improve and promote quality; demonstrates accuracy and thoroughness.
- Innovation - meets challenges with resourcefulness; generates suggestions for improving work; develops innovative approaches and ideas.
- Oral Communication - speaks clearly; listens and gets clarification; responds well to questions; demonstrates good presentation skills; participates effectively in meetings.
- Written Communication - writes clearly and informatively; edits work for spelling and grammar; varies writing style to meet needs; presents numerical data effectively; able to read and interpret written information.
Job Responsibilities
- Responsible for GxP compliance within designated processing areas.
- Accountable for safety of self and team within designated processing areas.
Experience / Professional Background
- Fluent English language (written and oral).
- Competency and familiarity with basic IT systems (e.g. Microsoft Office, etc.).
- Previous experience in a GMP manufacturing environment (preferred not mandatory).
Shift Outline
The role entails shift work as follows:
- Early Shift: 07:00 – 15:00pm
- Late Shift: 15:00-23:00pm
- (Rotating shift pattern; week 1 Early, week 2 lates, week 3 Early, week 4 lates etc .).
- You many also be temporarily required to work a regular day shift 08:30 – 16:30pm or a 12-hour day shift 07:00-19:00pm between the rotating shift patterns.
- As part of this role, you may also be required to work night shifts therefore in accepting the role you acknowledge that you may be required to work night shifts (12 or 8 hours depending on roster).
- Compensation for the above Shift Patterns, including the potential night work, will be in the form of a monthly Shift Premium.
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Manufacturing Technician
Posted 19 days ago
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Job Description
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
Manufacturing Technician
Posted 2 days ago
Job Viewed
Job Description
As the Manufacturing Technician you will be responsible for both the technical and hands-on aspects of day-to-day support of manufacturing processes on site, assist/write technical documents, validation protocols and report.
You will also be responsible for assisting in engineering studies for process improvements using Six Sigma principles and validations, designs and assists with the development and implementation of new/improved tooling, fixtures, processes, and equipment.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a **maker of possible** with us!
**Our vision for Peripheral Intervention (PI)** **at BD**
Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, end-stage renal disease and maintenance.
This role is offered on our night shift: Monday - Thursday 5pm - 3.15am and offers a 25% shift premium (Occasional Friday shifts will also be required)
**Main responsibilities will include:**
+ To support production on a daily basis and ensure minimal downtime due to equipment/machine issues.
+ Assists in the generation/execution of test protocols and procedures.
+ Sets up and operates manufacturing and/or test equipment. Records data with limited supervision.
+ Maintains accurate data and organizes and presents data in a reportable format.
+ Develops and maintains a working knowledge of BD Enniscorthy's policies and procedures and ISO and FDA requirements.
+ Completes calibration/maintenance activities as per schedule Monthly.
+ Completes actions generated from GMP audits.
+ Responsible for executing/assisting in the development, implementation and continuous improvement of processes and equipment to produce products that meet customer requirements and are cost effective.
+ Responsible for assisting in system assurance including documentation, testing and inspection, product and process development, and non-confirming product investigations.
+ Provides advice and feedback on corrective actions in a timely manner.
+ Work with engineering on functionality issues and procedure updates.
+ Communicate with engineering on equipment performance and functionality issues.
+ Helps monitor productivity by tracking equipment downtime issues.
+ Assists with the installation, debug, and validation of process equipment.
+ Maintain a clean/tidy and safe work area.
+ Follow all safety guidelines and report unsafe conditions to supervisor.
**About you:**
+ Achieve leaving Certificate (or equivalent) with passes in 5 subjects, including Maths and English/Irish.
+ QQI Level 6 Higher Certificate in Manufacturing Engineering or related discipline is distinct advantage.
+ Have a fundamental understanding of mechanical, electrical, and other utility systems.
+ Ability to problem solve electrical, software and mechanical issues in a timely fashion
+ Ability to deep dive and use a logical approach to fault find.
+ Proficiency in personal computer software (Microsoft Office and Excel).
+ Experience using Blue Mountain RAM or equivalent Preventative Maintenance system
+ Ability to work as part of a dynamic team and poses excellent communication skills.
+ Good Organisational skills and daily work planning.
Click on apply if this sounds like you!
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
To learn more about BD visit: Skills
Optional Skills
.
**Primary Work Location**
IRL Wexford - Enniscorthy
**Additional Locations**
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
35,700.00 - 60,700.00 EUR Annual
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
Manufacturing Technician
Posted 16 days ago
Job Viewed
Job Description
We are currently recruiting for Manufacturing Technicians across area's such as Surface Mount Technology, E Beam, Packing and Puck. In this role you will provide technical support relating to equipment utilized in the manufacturing areas by repairing, maintaining, or modifying production equipment utilizing technical expertise, technical manuals, schematic drawings, precision tools, and test equipment. You will utilize data reports on equipment and systems to generate improvement initiatives, monitor machine output on the shift to and ensure all cells are running to cycle time, to meet specific OEE targets. Perform and/or participate with conducting routine maintenance checks to ensure the operational efficiency of machines and production equipment is maintained to the desired standards. Monitor processes, running diagnostic tests with products and equipment, create a comprehensive report for resolution methods, familiar with asset maintenance software (Maximo preferable).
Your main responsibilities will be:
+ Activities include conducting scheduled maintenance, diagnosing, and troubleshooting faults and undertaking repairs, and selecting, engaging, and working with outside contractors.
+ Performs the most complex skilled maintenance and repair such as mechanical, pneumatics, electrical systems.
+ Ability to interpret blueprints and schematics.
+ Good understanding on day-to-day operation for conveyors, depositors, p&p machines, and weighing machines.
+ Assist in the compilation and presentation of technical feedback on engineering performance relating to yield output.
+ Lead on maintenance and/or process issues and to work independently or as a team member.
+ Monitor production processes, running diagnostic tests with products and equipment, and create a comprehensive report for resolution methods
+ Certifies and train manufacturing associates in the production processes.
+ Evaluate operating data to conduct on-line adjustments to products, instruments, or equipment. May develop or revise documents and procedures.
+ Identifies and implements corrective actions for manufacturing related issues.
+ Installs and validates equipment and processes in the production area to improve yield and/or reduce cycle time following the established validation procedure.
**QUALIFICATIONS AND EXPERIENCE**
+ Min level 6 in technical related discipline.
+ Electrical and mechanical skills are desired.
+ Must have excellent knowledge with industrial machines and the mechanical industry, as their expertise is crucial in keeping the safety and security of all production staff.
+ Experience within a Computerized Maintenance Management Work Order system environment.
+ Technical and fault-finding skills
+ Surface mount technology experience an advantage.
**What we Offer**
Attractive compensation package that includes competitive pay, as well as benefits such as
+ Family health insurance,
+ Excellent pension scheme
+ Life assurance
+ Career Development
+ Fantastic new facility
+ Growing business plus access to many more benefits.
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