255 Installation & Maintenance jobs in Ireland
Maintenance Team Lead
Abbott
Posted 1 day ago
Job Viewed
Job Description
**Work with Purpose - Join Abbott Donegal as a Process Lead**
At Abbott, we help people live more fully at all stages of life. With over 109,000 colleagues serving in 160+ countries, we deliver life-changing technologies across diagnostics, medical devices, nutrition, and branded medicines.
In Ireland, Abbott employs 6,000 people across 10 sites, including our Donegal Town facility, where almost 700 team members manufacture FreeStyle blood glucose test strips and sensors used in diabetes care worldwide.
As a Process Lead, you'll lead production teams in a state-of-the-art cleanroom environment, drive continuous improvement, and help deliver products that make a real difference in people's lives. You'll also be given opportunities and encouragement to grow your career, with access to development programs and support to help you reach your full potential.
**Why This Role Matters:**
Your leadership will directly impact the quality, efficiency, and reliability of products that support millions of people managing diabetes. You'll help shape a culture of excellence, safety, and innovation-ensuring our operations run smoothly and our teams thrive.
**What You'll Do:**
+ Manage daily production activities and support a team of operators.
+ Solve equipment and process issues to keep operations running efficiently.
+ Lead continuous improvement initiatives and coach team members.
+ Ensure compliance with SOPs, training standards, and safety policies.
+ Collaborate across departments and drive performance against key metrics.
**What Success Looks Like:**
+ You adapt quickly, solve problems creatively, and persist through challenges.
+ You anticipate trends, think critically, and make sound decisions-even with limited information.
+ You build trust, foster inclusive teams, and put the right people in the right roles.
+ You seek real-time feedback, challenge assumptions, and communicate with impact.
+ You turn data into meaningful actions and create space for tough conversations early.
+ You support and develop diverse talent, putting team needs ahead of personal interests.
**What You'll Bring:**
+ A third-level qualification or trade certificate in Engineering, Science, or Manufacturing.
+ 3+ years' experience in a manufacturing or engineering environment.
+ Strong communication, multitasking, and leadership skills.
+ A passion for continuous improvement and making an impact.
**Ready to lead with purpose, grow your career, and help shape the future of healthcare?**
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
At Abbott, we help people live more fully at all stages of life. With over 109,000 colleagues serving in 160+ countries, we deliver life-changing technologies across diagnostics, medical devices, nutrition, and branded medicines.
In Ireland, Abbott employs 6,000 people across 10 sites, including our Donegal Town facility, where almost 700 team members manufacture FreeStyle blood glucose test strips and sensors used in diabetes care worldwide.
As a Process Lead, you'll lead production teams in a state-of-the-art cleanroom environment, drive continuous improvement, and help deliver products that make a real difference in people's lives. You'll also be given opportunities and encouragement to grow your career, with access to development programs and support to help you reach your full potential.
**Why This Role Matters:**
Your leadership will directly impact the quality, efficiency, and reliability of products that support millions of people managing diabetes. You'll help shape a culture of excellence, safety, and innovation-ensuring our operations run smoothly and our teams thrive.
**What You'll Do:**
+ Manage daily production activities and support a team of operators.
+ Solve equipment and process issues to keep operations running efficiently.
+ Lead continuous improvement initiatives and coach team members.
+ Ensure compliance with SOPs, training standards, and safety policies.
+ Collaborate across departments and drive performance against key metrics.
**What Success Looks Like:**
+ You adapt quickly, solve problems creatively, and persist through challenges.
+ You anticipate trends, think critically, and make sound decisions-even with limited information.
+ You build trust, foster inclusive teams, and put the right people in the right roles.
+ You seek real-time feedback, challenge assumptions, and communicate with impact.
+ You turn data into meaningful actions and create space for tough conversations early.
+ You support and develop diverse talent, putting team needs ahead of personal interests.
**What You'll Bring:**
+ A third-level qualification or trade certificate in Engineering, Science, or Manufacturing.
+ 3+ years' experience in a manufacturing or engineering environment.
+ Strong communication, multitasking, and leadership skills.
+ A passion for continuous improvement and making an impact.
**Ready to lead with purpose, grow your career, and help shape the future of healthcare?**
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
0
Site Services Operator
Dublin, Leinster
WM
Posted 2 days ago
Job Viewed
Job Description
**About Us:**
Stericycle is a U.S. based business-to-business services company and leading provider of compliance-based solutions that protects people and brands, promotes health and well-being, and safeguards the environment. Since our founding over 30 years ago, we have grown from a small start-up in medical waste management into a leader across a range of increasingly complex and highly regulated arenas, serving healthcare organizations and commercial businesses of every size. Every day, we help our customers solve complex challenges by safely managing materials that could otherwise spread disease, contaminate the environment, or compromise one's identity.
Join us on our mission to protect health and well-being in a safe, responsible, and sustainable way.
**Position Purpose:**
To travel to customer sites to prepare, pack and transport hazardous clinical and chemical waste destined for the Kylemore Road facility.
**Key Job Activities:**
Preparation and packing of hazardous clinical and chemical waste on customer sites.
Awareness of, and adherence to all customer site safety rules.
Ensure all waste containers received meet the required standards, e.g., UN approval, clean/safe condition.
Checking of all paperwork, consignment notes & route sheets to ensure information is correct.
Ensure all assigned stock is correct for the job and all usage is accounted for.
Be available to travel to customer sites and stay overnight if necessary.
Report any health and safety concerns to management and/or supervisors.
Ensure the highest quality standards are adhered to.
Ensure company vehicle is in good working order and has all required safety equipment onboard.
Any other duties deemed reasonable to complete assigned tasks.
Follow all company Standard Operating Procedures.
Observe and enforce Health & Safety rules and work to maintain a safe working environment.
**Education:**
Required Education: High School or equivalent.
**Experience (EMEAA):**
Preferred Experience: In-depth knowledge & understanding of plant operations.
Required: Driving licence, ADR Training, Chemical Awareness Training, Safe Pass, Manual Handling, Forklift training. HazChem Training in the transport of dangerous goods is also required.
Physically fit
Safe Pass
Excellent communication skills
Computer literacy
Ability to work alone or as part of a team
Previous experience of using a Forklift truck.
**Certifications and/or Licenses:**
**Benefits:**
Stericycle offers you:
+ Contributory Pension Scheme
+ Life Insurance
+ Access to SteriCares, our employee support fund
+ Stericycle University - Our online library of self-development & learning
+ Annual performance related pay review.
+ Referral Scheme (Earn by introducing people in your network to the Stericycle family)
+ Flu voucher
+ Eye Test voucher
And more.
**_Disclaimer:_**
The above description is meant to provide a summary of the nature and level of work being performed; it should not be construed as an exhaustive list of all responsibilities, duties and requirements of the job. This document does not create an employment contract, implied or otherwise, and it does not constitute any right or guarantee of employment condition. This position is open to people with disabilities. Stericycle will consider requests for workplace accommodations for protected physical or mental limitations in accordance with its human resources and risks prevention policies and local laws. To the extent permissible under local law, and consistent with business necessity, Stericycle reserves the right to modify the content formally or informally, either verbally or in writing, at any time with or without advance notice.
Stericycle is a U.S. based business-to-business services company and leading provider of compliance-based solutions that protects people and brands, promotes health and well-being, and safeguards the environment. Since our founding over 30 years ago, we have grown from a small start-up in medical waste management into a leader across a range of increasingly complex and highly regulated arenas, serving healthcare organizations and commercial businesses of every size. Every day, we help our customers solve complex challenges by safely managing materials that could otherwise spread disease, contaminate the environment, or compromise one's identity.
Join us on our mission to protect health and well-being in a safe, responsible, and sustainable way.
**Position Purpose:**
To travel to customer sites to prepare, pack and transport hazardous clinical and chemical waste destined for the Kylemore Road facility.
**Key Job Activities:**
Preparation and packing of hazardous clinical and chemical waste on customer sites.
Awareness of, and adherence to all customer site safety rules.
Ensure all waste containers received meet the required standards, e.g., UN approval, clean/safe condition.
Checking of all paperwork, consignment notes & route sheets to ensure information is correct.
Ensure all assigned stock is correct for the job and all usage is accounted for.
Be available to travel to customer sites and stay overnight if necessary.
Report any health and safety concerns to management and/or supervisors.
Ensure the highest quality standards are adhered to.
Ensure company vehicle is in good working order and has all required safety equipment onboard.
Any other duties deemed reasonable to complete assigned tasks.
Follow all company Standard Operating Procedures.
Observe and enforce Health & Safety rules and work to maintain a safe working environment.
**Education:**
Required Education: High School or equivalent.
**Experience (EMEAA):**
Preferred Experience: In-depth knowledge & understanding of plant operations.
Required: Driving licence, ADR Training, Chemical Awareness Training, Safe Pass, Manual Handling, Forklift training. HazChem Training in the transport of dangerous goods is also required.
Physically fit
Safe Pass
Excellent communication skills
Computer literacy
Ability to work alone or as part of a team
Previous experience of using a Forklift truck.
**Certifications and/or Licenses:**
**Benefits:**
Stericycle offers you:
+ Contributory Pension Scheme
+ Life Insurance
+ Access to SteriCares, our employee support fund
+ Stericycle University - Our online library of self-development & learning
+ Annual performance related pay review.
+ Referral Scheme (Earn by introducing people in your network to the Stericycle family)
+ Flu voucher
+ Eye Test voucher
And more.
**_Disclaimer:_**
The above description is meant to provide a summary of the nature and level of work being performed; it should not be construed as an exhaustive list of all responsibilities, duties and requirements of the job. This document does not create an employment contract, implied or otherwise, and it does not constitute any right or guarantee of employment condition. This position is open to people with disabilities. Stericycle will consider requests for workplace accommodations for protected physical or mental limitations in accordance with its human resources and risks prevention policies and local laws. To the extent permissible under local law, and consistent with business necessity, Stericycle reserves the right to modify the content formally or informally, either verbally or in writing, at any time with or without advance notice.
This advertiser has chosen not to accept applicants from your region.
1
Maintenance Engineer
Dublin, Leinster
WM
Posted 2 days ago
Job Viewed
Job Description
**About Us:**
Stericycle is a U.S. based business-to-business services company and leading provider of compliance-based solutions that protects people and brands, promotes health and well-being, and safeguards the environment. Since our founding over 30 years ago, we have grown from a small start-up in medical waste management into a leader across a range of increasingly complex and highly regulated arenas, serving healthcare organizations and commercial businesses of every size. Every day, we help our customers solve complex challenges by safely managing materials that could otherwise spread disease, contaminate the environment, or compromise one's identity.
Join us on our mission to protect health and well-being in a safe, responsible, and sustainable way.
**Position Purpose:**
Responsible for the day to day maintenance activities within the plant to keep downtime to a minimum using preventive and reactive maintenance procedures in line with site specific maintenance schedules. Ensure that the plant availability is optimised through constant and sustained programmes of maintenance to company safety and operational procedures and fully comply with HSE legislation and WID regulations. To carry out planned and breakdown maintenance at the plant prioritising works utilising the onsite defect reporting system and in agreement with the Shift Supervisor or Plant Manager. To assist in the operation of the planned maintenance system, including appropriate record keeping either by electronic or other means. Contribution to the forward planning of shut down and capital works within the operational site confines is of paramount importance.
**Key Job Activities:**
To provide first line breakdown/defect repairs and or support to Shift Supervisors, acting immediately and effectively to minimize the loss of plant availability.
To closely monitor the safe running of the plant and report to the Supervisor or Manager any engineering concerns.
To inspect, co-ordinate and maintain the plant maintenance documentation in conjunction with the Plant Manager.
To prepare and co-ordinate the inspection and effective repairs if required to all statutory and non-statutory testing actions required to plant and equipment.
To review and update where required or as and when necessary site maintenance procedures (site specific).
To ensure pending unsafe conditions are note and reported to the Plant Manager.
To maintain the workshop area and subsequent spares availability to ensure minimum downtime.
To provide the Plant Manager with appropriate stock lists as and when required for audit purposes.
To be involved with the 'out of hours' engineering support group in providing frontline maintenance support both commercially and physically when required.
To liaise with the Plant manager on improvement initiatives for company equipment.
To complete maintenance logs in line with company system.
To stand in for Shift Supervisor in their absence (site specific requirement).
**Education:**
Required Education: High School or equivalent.
Preferred Education: Bachelor's or equivalent.
**Experience (EMEAA):**
3+ Years of Experience.
Broad extensive knowledge of theories and techniques of a function.
Minimum requirement formal qualification in Mechanical Engineering (e.g. City & Guilds or equivalent) Hydraulics maintenance / fault finding.
Working Knowledge of steam systems on a waste to energy plant.
Pneumatics experience.
Welding MMA/MIG/TIG experience.
Oxy/propane cutting experience.
Electrical fault-finding experience (desirable)
16th/17th Edition Electrical Qualification (desirable)
FLT Licence
Heavy industrial plant experience (desirable)
A willingness to develop in the role.
Robotics
**Certifications and/or Licenses:**
**Benefits:**
Stericycle offers you:
+ Contributory Pension Scheme
+ Life Insurance
+ Access to SteriCares, our employee support fund
+ Stericycle University - Our online library of self-development & learning
+ Annual performance related pay review.
+ Referral Scheme (Earn by introducing people in your network to the Stericycle family)
+ Flu voucher
+ Eye Test voucher
And more.
**_Disclaimer:_**
The above description is meant to provide a summary of the nature and level of work being performed; it should not be construed as an exhaustive list of all responsibilities, duties and requirements of the job. This document does not create an employment contract, implied or otherwise, and it does not constitute any right or guarantee of employment condition. This position is open to people with disabilities. Stericycle will consider requests for workplace accommodations for protected physical or mental limitations in accordance with its human resources and risks prevention policies and local laws. To the extent permissible under local law, and consistent with business necessity, Stericycle reserves the right to modify the content formally or informally, either verbally or in writing, at any time with or without advance notice.
Stericycle is a U.S. based business-to-business services company and leading provider of compliance-based solutions that protects people and brands, promotes health and well-being, and safeguards the environment. Since our founding over 30 years ago, we have grown from a small start-up in medical waste management into a leader across a range of increasingly complex and highly regulated arenas, serving healthcare organizations and commercial businesses of every size. Every day, we help our customers solve complex challenges by safely managing materials that could otherwise spread disease, contaminate the environment, or compromise one's identity.
Join us on our mission to protect health and well-being in a safe, responsible, and sustainable way.
**Position Purpose:**
Responsible for the day to day maintenance activities within the plant to keep downtime to a minimum using preventive and reactive maintenance procedures in line with site specific maintenance schedules. Ensure that the plant availability is optimised through constant and sustained programmes of maintenance to company safety and operational procedures and fully comply with HSE legislation and WID regulations. To carry out planned and breakdown maintenance at the plant prioritising works utilising the onsite defect reporting system and in agreement with the Shift Supervisor or Plant Manager. To assist in the operation of the planned maintenance system, including appropriate record keeping either by electronic or other means. Contribution to the forward planning of shut down and capital works within the operational site confines is of paramount importance.
**Key Job Activities:**
To provide first line breakdown/defect repairs and or support to Shift Supervisors, acting immediately and effectively to minimize the loss of plant availability.
To closely monitor the safe running of the plant and report to the Supervisor or Manager any engineering concerns.
To inspect, co-ordinate and maintain the plant maintenance documentation in conjunction with the Plant Manager.
To prepare and co-ordinate the inspection and effective repairs if required to all statutory and non-statutory testing actions required to plant and equipment.
To review and update where required or as and when necessary site maintenance procedures (site specific).
To ensure pending unsafe conditions are note and reported to the Plant Manager.
To maintain the workshop area and subsequent spares availability to ensure minimum downtime.
To provide the Plant Manager with appropriate stock lists as and when required for audit purposes.
To be involved with the 'out of hours' engineering support group in providing frontline maintenance support both commercially and physically when required.
To liaise with the Plant manager on improvement initiatives for company equipment.
To complete maintenance logs in line with company system.
To stand in for Shift Supervisor in their absence (site specific requirement).
**Education:**
Required Education: High School or equivalent.
Preferred Education: Bachelor's or equivalent.
**Experience (EMEAA):**
3+ Years of Experience.
Broad extensive knowledge of theories and techniques of a function.
Minimum requirement formal qualification in Mechanical Engineering (e.g. City & Guilds or equivalent) Hydraulics maintenance / fault finding.
Working Knowledge of steam systems on a waste to energy plant.
Pneumatics experience.
Welding MMA/MIG/TIG experience.
Oxy/propane cutting experience.
Electrical fault-finding experience (desirable)
16th/17th Edition Electrical Qualification (desirable)
FLT Licence
Heavy industrial plant experience (desirable)
A willingness to develop in the role.
Robotics
**Certifications and/or Licenses:**
**Benefits:**
Stericycle offers you:
+ Contributory Pension Scheme
+ Life Insurance
+ Access to SteriCares, our employee support fund
+ Stericycle University - Our online library of self-development & learning
+ Annual performance related pay review.
+ Referral Scheme (Earn by introducing people in your network to the Stericycle family)
+ Flu voucher
+ Eye Test voucher
And more.
**_Disclaimer:_**
The above description is meant to provide a summary of the nature and level of work being performed; it should not be construed as an exhaustive list of all responsibilities, duties and requirements of the job. This document does not create an employment contract, implied or otherwise, and it does not constitute any right or guarantee of employment condition. This position is open to people with disabilities. Stericycle will consider requests for workplace accommodations for protected physical or mental limitations in accordance with its human resources and risks prevention policies and local laws. To the extent permissible under local law, and consistent with business necessity, Stericycle reserves the right to modify the content formally or informally, either verbally or in writing, at any time with or without advance notice.
This advertiser has chosen not to accept applicants from your region.
2
Stability Storage Technician
Athlone, Leinster
ThermoFisher Scientific
Posted 2 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Are you looking to be part of a top-tier team and make a difference in groundbreaking projects within an encouraging and diverse setting? Thermo Fisher Scientific Inc. is searching for an outstanding and dedicated Stability Storage Technician to join our team in Athlone, Ireland. This is an outstanding opportunity to work in a proven and innovative environment where your contributions will strictly determine our success!
**Responsibilities**
+ Ensure accurate preventative maintenance, qualification, calibration, and operation of temperature/humidity chambers, analytical instrumentation, environmental monitoring systems, and related equipment.
+ Independently complete assigned preventative maintenance, calibration, and qualification protocols.
+ Troubleshoot, document, and accurately address significant temperature/humidity chambers, analytical instrumentation, and related equipment anomalies.
**Requirements**
+ Strong troubleshooting skills to address and resolve equipment anomalies.
+ Collaborative approach to working effectively within a diverse team.
+ Outstanding documentation skills to ensure compliance and accuracy.
+ Familiarity with Microsoft Office including Word and Excel.
+ Ability to train and guide others on equipment use and maintenance.
+ Occasional on call requirements.
**The following would be an advantage**
+ GMP knowledge and understanding of FDA, ICH, and USP guidelines.
+ Familiarity with environmental monitoring systems.
+ Previous experience of addressing non-conformance and quality-related issues.
+ Knowledge of qualifications and validation procedures.
+ Previous experience of temperature mapping.
+ Familiarity with water treatment processes to meet laboratory standards.
Join us and be part of a team that values integrity, innovation, and involvement. At Thermo Fisher Scientific, we strictly adhere to the highest standards to ensure our customers can succeed in their missions. Your contributions will help us compete in a global market and implement solutions that make the world healthier, cleaner, and safer. Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Are you looking to be part of a top-tier team and make a difference in groundbreaking projects within an encouraging and diverse setting? Thermo Fisher Scientific Inc. is searching for an outstanding and dedicated Stability Storage Technician to join our team in Athlone, Ireland. This is an outstanding opportunity to work in a proven and innovative environment where your contributions will strictly determine our success!
**Responsibilities**
+ Ensure accurate preventative maintenance, qualification, calibration, and operation of temperature/humidity chambers, analytical instrumentation, environmental monitoring systems, and related equipment.
+ Independently complete assigned preventative maintenance, calibration, and qualification protocols.
+ Troubleshoot, document, and accurately address significant temperature/humidity chambers, analytical instrumentation, and related equipment anomalies.
**Requirements**
+ Strong troubleshooting skills to address and resolve equipment anomalies.
+ Collaborative approach to working effectively within a diverse team.
+ Outstanding documentation skills to ensure compliance and accuracy.
+ Familiarity with Microsoft Office including Word and Excel.
+ Ability to train and guide others on equipment use and maintenance.
+ Occasional on call requirements.
**The following would be an advantage**
+ GMP knowledge and understanding of FDA, ICH, and USP guidelines.
+ Familiarity with environmental monitoring systems.
+ Previous experience of addressing non-conformance and quality-related issues.
+ Knowledge of qualifications and validation procedures.
+ Previous experience of temperature mapping.
+ Familiarity with water treatment processes to meet laboratory standards.
Join us and be part of a team that values integrity, innovation, and involvement. At Thermo Fisher Scientific, we strictly adhere to the highest standards to ensure our customers can succeed in their missions. Your contributions will help us compete in a global market and implement solutions that make the world healthier, cleaner, and safer. Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
3
Maintenance Technician (Night Shift)
Dundalk, Leinster
PCI Pharma Services
Posted 2 days ago
Job Viewed
Job Description
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
We are now looking for a **Maintenance Technician** (Permanent role) to join our team in Dundalk, County Louth.
This is a **Night Shift** role, covering Monday to Wednesday 12 hours shift (7pm to 7am).
**Summary of Role:**
+ Responsible for ensuring machine change over's, stoppages and breakdowns are undertaken in a timely manner to targets and with minimum disruption to production schedules.
+ Undertake planned routine maintenance and maintain schedules ensuring that all equipment and plant are able to operate safely, efficiently, and in compliance with GMP practices.
+ Fault find to an expert level on Electrical and Mechanical systems.
+ Multiskilled able to program PLC's and to participate in technically involved projects to improve or create new processes.
+ Mechanically able to design systems and develop to implementation.
+ Implement continuous improvements on equipment and carry out to a high standard within GMP guidelines.
+ Create MOC's and manage through the QMS.
+ Create design of experiments and use other fault-finding techniques to improve processes.
**Responsibilities:**
+ Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
+ Ensure that maintenance areas and equipment are kept in a clean, tidy and secure state (including storage areas).
+ Adherence and recording of defined routine maintenance schedules; covering all equipment and plant.
+ Rapid and flexible attention to all breakdowns/stoppages to minimise loss of production, liaising with Engineering Supervisor and Operational Engineering Manager.
+ Carry out/Participate in A3 Problem solving activities on major issues and lead to Root cause.
+ Analysis of equipment redesign of any systems/equipment to improve process.
+ Planning and implementation of engineering improvement projects, designing and developing to Validation.
+ Advise Engineering Supervisor and Operational Engineering Manager of any machine or plant which requires major repair or maintenance.
+ Highlight potential areas for improvement within Production area regarding equipment or procedural changes.
+ Liaise with Production on identifying areas for continuous improvement and implement changes using correct change procedure.
+ Strip down, cleaning and reassembling of production equipment as per routine maintenance schedules.
+ Perform machine set-ups and changeovers to target times as required in line with production requirements.
+ To actively assist in looking at ways to improve changeover times by procedure and method.
+ Ensure the timely and accurate completion of all documentation and paperwork such as tooling logs, setting sheets, online working sheets, PPM sheets.
+ Improve and maintain the levels of current Good Manufacturing Practice.
+ Assist with the training of colleagues as required.
+ The use of workshop equipment to manufacture piece parts and repair as required.
+ Assist with projects on trials, and new product introductions as required.
+ Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
**Knowledge / Skills & Experience:**
**Essential:**
+ Bachelor's or Associate Degree or Diploma / Certificate in Engineering. May substitute experience in lieu of educational requirements.
+ 4 years' experience.
+ Proven track record of showing how results were delivered through management/leadership.
+ Capability to follow set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
+ Ability to manage multiple tasks.
+ Problem Solving and Troubleshooting skills. The successful candidate should display a dynamic and proactive approach to manage problems.
+ Self-motivated with a results driven approach.
+ Flexibility to work across different shifts on request in line with business needs.
+ Adaptable and ability to work collaboratively.
+ Proficient in Microsoft Office products (incl. Excel, PowerPoint, Word, etc.)
+ Take care of your own health and safety and that of people who may be affected by what you do (or do not do).
+ Co-operate with others on health and safety, and not interfere with, or misuse, anything provided for your health, safety, or welfare.
**Desirable:**
+ Experience in a GMP or Regulated Environment.
+ Experience in Lean Manufacturing, including experience in Lean tools to develop continuous improvements.
#LI-VR1
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services 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._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
We are now looking for a **Maintenance Technician** (Permanent role) to join our team in Dundalk, County Louth.
This is a **Night Shift** role, covering Monday to Wednesday 12 hours shift (7pm to 7am).
**Summary of Role:**
+ Responsible for ensuring machine change over's, stoppages and breakdowns are undertaken in a timely manner to targets and with minimum disruption to production schedules.
+ Undertake planned routine maintenance and maintain schedules ensuring that all equipment and plant are able to operate safely, efficiently, and in compliance with GMP practices.
+ Fault find to an expert level on Electrical and Mechanical systems.
+ Multiskilled able to program PLC's and to participate in technically involved projects to improve or create new processes.
+ Mechanically able to design systems and develop to implementation.
+ Implement continuous improvements on equipment and carry out to a high standard within GMP guidelines.
+ Create MOC's and manage through the QMS.
+ Create design of experiments and use other fault-finding techniques to improve processes.
**Responsibilities:**
+ Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
+ Ensure that maintenance areas and equipment are kept in a clean, tidy and secure state (including storage areas).
+ Adherence and recording of defined routine maintenance schedules; covering all equipment and plant.
+ Rapid and flexible attention to all breakdowns/stoppages to minimise loss of production, liaising with Engineering Supervisor and Operational Engineering Manager.
+ Carry out/Participate in A3 Problem solving activities on major issues and lead to Root cause.
+ Analysis of equipment redesign of any systems/equipment to improve process.
+ Planning and implementation of engineering improvement projects, designing and developing to Validation.
+ Advise Engineering Supervisor and Operational Engineering Manager of any machine or plant which requires major repair or maintenance.
+ Highlight potential areas for improvement within Production area regarding equipment or procedural changes.
+ Liaise with Production on identifying areas for continuous improvement and implement changes using correct change procedure.
+ Strip down, cleaning and reassembling of production equipment as per routine maintenance schedules.
+ Perform machine set-ups and changeovers to target times as required in line with production requirements.
+ To actively assist in looking at ways to improve changeover times by procedure and method.
+ Ensure the timely and accurate completion of all documentation and paperwork such as tooling logs, setting sheets, online working sheets, PPM sheets.
+ Improve and maintain the levels of current Good Manufacturing Practice.
+ Assist with the training of colleagues as required.
+ The use of workshop equipment to manufacture piece parts and repair as required.
+ Assist with projects on trials, and new product introductions as required.
+ Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company.
**Knowledge / Skills & Experience:**
**Essential:**
+ Bachelor's or Associate Degree or Diploma / Certificate in Engineering. May substitute experience in lieu of educational requirements.
+ 4 years' experience.
+ Proven track record of showing how results were delivered through management/leadership.
+ Capability to follow set clear goals, communicate these clearly and ensure progress to completion meeting predefined targets.
+ Ability to manage multiple tasks.
+ Problem Solving and Troubleshooting skills. The successful candidate should display a dynamic and proactive approach to manage problems.
+ Self-motivated with a results driven approach.
+ Flexibility to work across different shifts on request in line with business needs.
+ Adaptable and ability to work collaboratively.
+ Proficient in Microsoft Office products (incl. Excel, PowerPoint, Word, etc.)
+ Take care of your own health and safety and that of people who may be affected by what you do (or do not do).
+ Co-operate with others on health and safety, and not interfere with, or misuse, anything provided for your health, safety, or welfare.
**Desirable:**
+ Experience in a GMP or Regulated Environment.
+ Experience in Lean Manufacturing, including experience in Lean tools to develop continuous improvements.
#LI-VR1
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services 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._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
This advertiser has chosen not to accept applicants from your region.
4
Senior Supervisor, Maintenance
Cork, Munster
Stryker
Posted 2 days ago
Job Viewed
Job Description
Senior Supervisor, Maintenance (Stryker, Anngrove)
Position Summary
This is a senior supervisory role within the Maintenance function. The position carries direct responsibility for leading a team of technicians and engineers in delivering a high-performance maintenance program. The Senior Supervisor will ensure consistent execution of preventive and corrective maintenance activities across the site, with a strong focus on asset uptime, reliability, and continuous development of team capability. The role requires a technically strong leader with excellent interpersonal and communication skills to engage both the maintenance team and cross-functional stakeholders.
**Key Areas of Responsibility**
+ Responsible for the leadership and management of the Maintenance team, ensuring operational objectives are met through the delivery of a robust and efficient maintenance program.
+ Accountable for ensuring Preventive Maintenance (PM) activities are completed on schedule and to a high standard.
+ Oversee timely execution of Corrective Maintenance (CM), minimizing equipment downtime and maximizing overall equipment effectiveness.
+ Monitor, report, and act on key performance metrics, including Equipment Uptime, Mean Time To Failure (MTTF), and Mean Time To Repair (MTTR).
+ Ensure machine safety concerns are addressed promptly and effectively, supporting investigations and follow-up actions related to any safety incidents or hazards.
+ Lead continuous improvement initiatives within the maintenance function, using lean tools and root cause analysis to improve processes and performance.
+ Foster a culture of development through structured upskilling, technical training, and mentoring of technicians and engineers.
+ Develop Individual Development Plans (IDPs) and conduct performance reviews to support growth and engagement of team members.
+ Partner with Operations, Engineering, Quality, and other support functions to ensure maintenance requirements are integrated into business planning and execution.
+ Ensure team compliance with GMP, GDP, EHS, and other regulatory and safety requirements.
+ Represent the Maintenance department in cross-functional forums and site-wide initiatives.
+ Drive the use of Computerized Maintenance Management Systems (CMMS) for planning, execution, and reporting of all maintenance activities.
+ Provide out-of-hours and shutdown support as required, ensuring adequate response and continuity of operations.
+ Lead technical investigations and support cross-functional troubleshooting efforts to resolve chronic or complex equipment issues.
+ Support the integration of reliability engineering principles into the maintenance function, with a focus on proactive asset care, failure mode analysis, and predictive maintenance strategies.
**Qualifications Knowledge Skills**
+ Level 8 Degree in Engineering or related technical discipline.
+ Minimum of 6 years' experience in a manufacturing environment, with ideally 3 years in a supervisory or leadership role.
+ Experience in a regulated manufacturing environment highly advantageous.
+ Proven technical background in maintenance of production equipment, ideally within medical device, pharmaceutical, or high-tech manufacturing sectors.
+ Strong understanding of CMMS systems, equipment reliability metrics, and maintenance planning principles.
+ Good knowledge of GMP / FDA regulatory requirements and current Health and Safety Regulations legislation.
+ Demonstrated ability to lead, motivate, and develop diverse technical teams.
+ Excellent communication skills, with the ability to interface effectively across all levels of the organization.
+ Experience using lean tools and continuous improvement methodologies.
+ High level of emotional intelligence with strong coaching and people management skills.
+ Flexible and adaptable, with effective project management and prioritization capabilities.
+ Strong analytical and problem-solving skills with a structured, self-starting approach to work.
#IJ
This role will be posted for a minimum of 3 days.
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.
Position Summary
This is a senior supervisory role within the Maintenance function. The position carries direct responsibility for leading a team of technicians and engineers in delivering a high-performance maintenance program. The Senior Supervisor will ensure consistent execution of preventive and corrective maintenance activities across the site, with a strong focus on asset uptime, reliability, and continuous development of team capability. The role requires a technically strong leader with excellent interpersonal and communication skills to engage both the maintenance team and cross-functional stakeholders.
**Key Areas of Responsibility**
+ Responsible for the leadership and management of the Maintenance team, ensuring operational objectives are met through the delivery of a robust and efficient maintenance program.
+ Accountable for ensuring Preventive Maintenance (PM) activities are completed on schedule and to a high standard.
+ Oversee timely execution of Corrective Maintenance (CM), minimizing equipment downtime and maximizing overall equipment effectiveness.
+ Monitor, report, and act on key performance metrics, including Equipment Uptime, Mean Time To Failure (MTTF), and Mean Time To Repair (MTTR).
+ Ensure machine safety concerns are addressed promptly and effectively, supporting investigations and follow-up actions related to any safety incidents or hazards.
+ Lead continuous improvement initiatives within the maintenance function, using lean tools and root cause analysis to improve processes and performance.
+ Foster a culture of development through structured upskilling, technical training, and mentoring of technicians and engineers.
+ Develop Individual Development Plans (IDPs) and conduct performance reviews to support growth and engagement of team members.
+ Partner with Operations, Engineering, Quality, and other support functions to ensure maintenance requirements are integrated into business planning and execution.
+ Ensure team compliance with GMP, GDP, EHS, and other regulatory and safety requirements.
+ Represent the Maintenance department in cross-functional forums and site-wide initiatives.
+ Drive the use of Computerized Maintenance Management Systems (CMMS) for planning, execution, and reporting of all maintenance activities.
+ Provide out-of-hours and shutdown support as required, ensuring adequate response and continuity of operations.
+ Lead technical investigations and support cross-functional troubleshooting efforts to resolve chronic or complex equipment issues.
+ Support the integration of reliability engineering principles into the maintenance function, with a focus on proactive asset care, failure mode analysis, and predictive maintenance strategies.
**Qualifications Knowledge Skills**
+ Level 8 Degree in Engineering or related technical discipline.
+ Minimum of 6 years' experience in a manufacturing environment, with ideally 3 years in a supervisory or leadership role.
+ Experience in a regulated manufacturing environment highly advantageous.
+ Proven technical background in maintenance of production equipment, ideally within medical device, pharmaceutical, or high-tech manufacturing sectors.
+ Strong understanding of CMMS systems, equipment reliability metrics, and maintenance planning principles.
+ Good knowledge of GMP / FDA regulatory requirements and current Health and Safety Regulations legislation.
+ Demonstrated ability to lead, motivate, and develop diverse technical teams.
+ Excellent communication skills, with the ability to interface effectively across all levels of the organization.
+ Experience using lean tools and continuous improvement methodologies.
+ High level of emotional intelligence with strong coaching and people management skills.
+ Flexible and adaptable, with effective project management and prioritization capabilities.
+ Strong analytical and problem-solving skills with a structured, self-starting approach to work.
#IJ
This role will be posted for a minimum of 3 days.
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.
This advertiser has chosen not to accept applicants from your region.
5
Manufacturing Maintenance Planning Lead
Abbott
Posted 2 days ago
Job Viewed
Job Description
**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, nutritional 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.
**Abbott Ireland Diabetes Care Division Donegal**
The Abbott Diabetes Care division based in Donegal Town manufactures FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre system.
**Primary Function:**
You are process and system driven and a proven ability to communicate effectively across multiple levels of the organisation. You can assess corrective maintenance and work with engineers and technicians to determine the right actions, spares and people to correct problems. You have a methodical approach and work closely with schedulers to ensure work can be planned and scheduled effectively, with a right first time approach. You have experience working in a regulated environment.
**Main Responsibilities:**
+ Work with Maximo system administrator to develop and manage KPIs and metrics relating to engineering services (and production as required). Plan corrective and preventive maintenance activities by task and priority level:
+ Ensure all EHS/Quality and reliability aspects are considered.
+ Ensure appropriate parts and tools are available.
+ Prepare all permits as required to maintenance activity.
+ Consult with technicians where necessary on corrective work required following PMs or equipment outage.
+ Coordinate with scheduler to ensure PMs and DMs are completed in timely fashion. Manage spare parts and alignment between the maintenance department and stock room. Manage work orders, documentation, and assets within the computerized maintenance management system (CMMS). Engage with contractors as required and ensure all reports, job cards, etc are completed fully in Maximo. Other related tasks as necessary.
+ Manage spares budget to ensure spares budget is adhered too. This includes forecasting and monitoring spend at LBE cycles and on a month-to-month basis.
+ Lead CFT's within Engineering and Operations to annually review reorder points to ensure the correct stock levels are adhered too.
+ Lead the introduction of new process improvement projects ensuring end to end user integration.
+ Lead the onboarding of new production lines to the manufacturing facility.
**Education & Years of Experience:**
+ Third level qualification in engineering/ Science/ Manufacturing/ Supply Chain discipline.
+ Two years work experience in an engineering/ manufacturing environment preferred.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Abbott is a global healthcare leader 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, nutritional 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.
**Abbott Ireland Diabetes Care Division Donegal**
The Abbott Diabetes Care division based in Donegal Town manufactures FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre system.
**Primary Function:**
You are process and system driven and a proven ability to communicate effectively across multiple levels of the organisation. You can assess corrective maintenance and work with engineers and technicians to determine the right actions, spares and people to correct problems. You have a methodical approach and work closely with schedulers to ensure work can be planned and scheduled effectively, with a right first time approach. You have experience working in a regulated environment.
**Main Responsibilities:**
+ Work with Maximo system administrator to develop and manage KPIs and metrics relating to engineering services (and production as required). Plan corrective and preventive maintenance activities by task and priority level:
+ Ensure all EHS/Quality and reliability aspects are considered.
+ Ensure appropriate parts and tools are available.
+ Prepare all permits as required to maintenance activity.
+ Consult with technicians where necessary on corrective work required following PMs or equipment outage.
+ Coordinate with scheduler to ensure PMs and DMs are completed in timely fashion. Manage spare parts and alignment between the maintenance department and stock room. Manage work orders, documentation, and assets within the computerized maintenance management system (CMMS). Engage with contractors as required and ensure all reports, job cards, etc are completed fully in Maximo. Other related tasks as necessary.
+ Manage spares budget to ensure spares budget is adhered too. This includes forecasting and monitoring spend at LBE cycles and on a month-to-month basis.
+ Lead CFT's within Engineering and Operations to annually review reorder points to ensure the correct stock levels are adhered too.
+ Lead the introduction of new process improvement projects ensuring end to end user integration.
+ Lead the onboarding of new production lines to the manufacturing facility.
**Education & Years of Experience:**
+ Third level qualification in engineering/ Science/ Manufacturing/ Supply Chain discipline.
+ Two years work experience in an engineering/ manufacturing environment preferred.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
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6
Technical Services Specialist
Kilkenny, Leinster
Abbott
Posted 2 days ago
Job Viewed
Job Description
**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.
**Abbott Diabetes Care Kilkenny**
Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems.
**Main Purpose of the Role:**
The Technical Services Specialist is responsible for conducting thorough investigations into technical issues and product failures to identify root causes and implement effective corrective and preventive actions. This role requires strong analytical skills, attention to detail, and the ability to collaborate across cross-functional teams to ensure product quality, reliability, and compliance with industry standards. This is a dynamic, multi-disciplinary role, requiring the ability to multi-task, prioritise, and work on own initiative with minimal oversight. The Technical Services Specialist will support the Materials Engineering Manager and wider technical and cross-functional teams, working closely with various ADC stakeholders including Operations, Quality, Controls Systems, Global Engineering, Validation and PMO.
**MAIN RESPONSIBILITIES**
+ Root Cause Analysis: Perform detailed investigations into product failures, process nonconformities, customer complaints, or system anomalies using structured methodologies (e.g., 5 Whys, Fishbone, RCA).
+ Data Analysis: Collect, analyse, and interpret technical data, test results, and performance metrics to identify trends and underlying issues.
+ Collaboration: Work closely with engineering, operations, and quality assurance teams to gather insights and validate findings.
+ Corrective Actions: Develop, recommend, and implement corrective and preventive actions (CAPA) to resolve issues and mitigate future risks.
+ Documentation: Prepare clear, concise, and detailed investigation reports, including findings, root cause analysis, and proposed solutions, ensuring compliance with regulatory and organizational standards.
+ Testing & Validation: Design and execute tests or simulations to replicate issues, validate hypotheses, and verify the effectiveness of solutions.
+ Process Improvement: Identify opportunities to enhance processes, tools, or systems to prevent recurrence of issues and improve overall quality.
+ Compliance: Ensure investigations and solutions adhere to industry regulations, standards, and internal policies (e.g., ISO, FDA, or other relevant frameworks).
+ Training & Knowledge Sharing: Provide guidance and training to teams on investigation techniques, best practices, and lessons learned.
+ Support the development of new processes to ensure the smooth running of the materials function and effective integration with other cross-functional processes.
+ Working with the OpEx team, support the development of Power BI trackers and dashboards to capture relevant materials KPIs and metrics.
+ Apply LEAN methodologies to drive operational excellence
+ Participate in cross-functional activities as necessary, to ensure continual improvement, safety and compliance.
+ Identify areas of improvement and risk.
+ Ensure compliance with industry standards and global regulations.
+ Learn, challenge, develop and maintain a working knowledge of Abbott Quality Policy and Procedures
**Qualifications & Experience:**
+ _Bachelor's degree in Engineering or equivalent technical discipline._
+ _3-5 years of experience in engineering, quality assurance, or a related field, with a focus on investigations, root cause analysis, or failure analysis._
+ _Technical Skills:_
+ _Proficiency in analytical tools and methodologies (e.g., RCA, FMEA, Statistical Process Control)._
+ _Familiarity with data analysis software._
+ _Soft Skills:_
+ _Strong problem-solving and critical-thinking abilities._
+ _Excellent communication skills, both written and verbal, for technical and non-technical audiences._
+ _Ability to work independently and collaboratively in a fast-paced environment._
+ Preferred but not required: Six Sigma Green/Black Belt.
**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 and on LinkedIn , Facebook , Instagram , X and YouTube .
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
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.
**Abbott Diabetes Care Kilkenny**
Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems.
**Main Purpose of the Role:**
The Technical Services Specialist is responsible for conducting thorough investigations into technical issues and product failures to identify root causes and implement effective corrective and preventive actions. This role requires strong analytical skills, attention to detail, and the ability to collaborate across cross-functional teams to ensure product quality, reliability, and compliance with industry standards. This is a dynamic, multi-disciplinary role, requiring the ability to multi-task, prioritise, and work on own initiative with minimal oversight. The Technical Services Specialist will support the Materials Engineering Manager and wider technical and cross-functional teams, working closely with various ADC stakeholders including Operations, Quality, Controls Systems, Global Engineering, Validation and PMO.
**MAIN RESPONSIBILITIES**
+ Root Cause Analysis: Perform detailed investigations into product failures, process nonconformities, customer complaints, or system anomalies using structured methodologies (e.g., 5 Whys, Fishbone, RCA).
+ Data Analysis: Collect, analyse, and interpret technical data, test results, and performance metrics to identify trends and underlying issues.
+ Collaboration: Work closely with engineering, operations, and quality assurance teams to gather insights and validate findings.
+ Corrective Actions: Develop, recommend, and implement corrective and preventive actions (CAPA) to resolve issues and mitigate future risks.
+ Documentation: Prepare clear, concise, and detailed investigation reports, including findings, root cause analysis, and proposed solutions, ensuring compliance with regulatory and organizational standards.
+ Testing & Validation: Design and execute tests or simulations to replicate issues, validate hypotheses, and verify the effectiveness of solutions.
+ Process Improvement: Identify opportunities to enhance processes, tools, or systems to prevent recurrence of issues and improve overall quality.
+ Compliance: Ensure investigations and solutions adhere to industry regulations, standards, and internal policies (e.g., ISO, FDA, or other relevant frameworks).
+ Training & Knowledge Sharing: Provide guidance and training to teams on investigation techniques, best practices, and lessons learned.
+ Support the development of new processes to ensure the smooth running of the materials function and effective integration with other cross-functional processes.
+ Working with the OpEx team, support the development of Power BI trackers and dashboards to capture relevant materials KPIs and metrics.
+ Apply LEAN methodologies to drive operational excellence
+ Participate in cross-functional activities as necessary, to ensure continual improvement, safety and compliance.
+ Identify areas of improvement and risk.
+ Ensure compliance with industry standards and global regulations.
+ Learn, challenge, develop and maintain a working knowledge of Abbott Quality Policy and Procedures
**Qualifications & Experience:**
+ _Bachelor's degree in Engineering or equivalent technical discipline._
+ _3-5 years of experience in engineering, quality assurance, or a related field, with a focus on investigations, root cause analysis, or failure analysis._
+ _Technical Skills:_
+ _Proficiency in analytical tools and methodologies (e.g., RCA, FMEA, Statistical Process Control)._
+ _Familiarity with data analysis software._
+ _Soft Skills:_
+ _Strong problem-solving and critical-thinking abilities._
+ _Excellent communication skills, both written and verbal, for technical and non-technical audiences._
+ _Ability to work independently and collaboratively in a fast-paced environment._
+ Preferred but not required: Six Sigma Green/Black Belt.
**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 and on LinkedIn , Facebook , Instagram , X and YouTube .
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
This advertiser has chosen not to accept applicants from your region.
7
Manufacturing/Maintenance Technician - Kilkenny
Kilkenny, Leinster
Abbott
Posted 2 days ago
Job Viewed
Job Description
**This is how you can make a difference at Abbott:**
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
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
This advertiser has chosen not to accept applicants from your region.
8
Field Service Engineer
Dublin, Leinster
Edwards Lifesciences
Posted 2 days ago
Job Viewed
Job Description
The Field Service Engineer will be responsible for the comprehensive management of the Cordella System, focusing on installation, technical support, and system optimization at clinical sites and patient homes. This role provides critical technical expertise and ensures high performance of the Cordella System by leading system installations, troubleshooting, and maintenance. The Field Service Engineer will serve as a key technical resource, ensuring successful system implementation while collaborating with cross-functional teams to drive continuous improvements in system performance and user experience.
**How you'll make an impact:**
**1. System Installation and Configuration**
+ Lead the **on-site installation** of the Cordella system in hospitals, verification of product performance in catheterization labs, and patient homes, ensuring seamless operation.
+ Oversee **system setup** before clinical use, including **system configuration.**
+ Conduct **pre-procedural equipment checks** to ensure systems are operational before Cordella implant procedures.
**2. Preventive Maintenance and System Health**
+ Perform **preventive maintenance** to optimize performance and prevent downtime.
+ Provide **technical troubleshooting** and on-site support to resolve any system-related issues promptly.
+ Manage and deploy **software and firmware updates** , ensuring compatibility and system efficiency.
**3. Cross-functional Collaboration and Reporting**
+ Collaborate with **R&D, Clinical Specialists, and Quality teams** to report system performance data, identify trends, and suggest areas for improvement.
+ Provide **detailed documentation** on system performance, error resolution, and user feedback to help refine product features and technical protocols.
+ Act as a liaison between **customers and internal teams** to facilitate system enhancements based on field feedback.
**What you'll need:**
+ **Education** :
+ Bachelor's degree in **Biomedical Engineering** , **Electrical Engineering** , or a related technical discipline. A master's degree is a plus.
+ **Experience** :
+ **3+ years** of experience as a field engineer, preferably with **medical devices** or health technology systems.
+ **Proven experience** in installing, maintaining, and troubleshooting complex systems in a healthcare or clinical environment.
+ **Technical Skills** :
+ **Deep knowledge** of medical devices, system integrations, and technical protocols.
+ **Hands-on experience** with clinical equipment, including calibration, setup, and troubleshooting.
+ Proficient in **software troubleshooting** , system diagnostics, and firmware updates.
+ **Communication Skills** :
+ Strong written and verbal communication skills for **effective technical documentation** and **customer interaction** .
+ **Problem-Solving & Analytical Abilities** :
+ Strong **troubleshooting** and **problem-solving** skills
+ Capable of **data analysis** for system performance and creating actionable reports for improvements.
+ **Travel** :
+ Willing to travel extensively across **Europe** to hospital sites and patient homes, with a flexible schedule for support during system failure events.
**What is it like to work at Edwards Lifesciences in Germany?**
As a global leader in patient-focused medical innovations, we offer rewarding opportunities and exciting challenges in a truly international, dynamic and friendly work environment.
We are committed to fostering a diverse and inclusive work environment where all employees can grow, personally and professionally. To achieve this, we offer on-the-job development, training opportunities and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).
Edwards Lifesciences in Germany also offers the following benefits:
+ Competitive Compensation and Benefits package
+ Flexible working hours, remote working
+ Pension plan Risk
+ Insurance Meal Benefits
+ Service Awards Enhanced
+ Leave Benefits
+ Transportation Benefits
+ Employee Stock Purchase Programme
+ Employee Assistance Programme
+ Comprehensive Wellness Programme including onsite gym, yoga classes and massage, preventive health checks, healthy lifestyle webinars, educational events, charity activities and much more.
Benefits are regulated by an internal policy which contains the full details regarding the entitlement and conditions for the benefits. Benefits policy and components may vary by location.
**How you'll make an impact:**
**1. System Installation and Configuration**
+ Lead the **on-site installation** of the Cordella system in hospitals, verification of product performance in catheterization labs, and patient homes, ensuring seamless operation.
+ Oversee **system setup** before clinical use, including **system configuration.**
+ Conduct **pre-procedural equipment checks** to ensure systems are operational before Cordella implant procedures.
**2. Preventive Maintenance and System Health**
+ Perform **preventive maintenance** to optimize performance and prevent downtime.
+ Provide **technical troubleshooting** and on-site support to resolve any system-related issues promptly.
+ Manage and deploy **software and firmware updates** , ensuring compatibility and system efficiency.
**3. Cross-functional Collaboration and Reporting**
+ Collaborate with **R&D, Clinical Specialists, and Quality teams** to report system performance data, identify trends, and suggest areas for improvement.
+ Provide **detailed documentation** on system performance, error resolution, and user feedback to help refine product features and technical protocols.
+ Act as a liaison between **customers and internal teams** to facilitate system enhancements based on field feedback.
**What you'll need:**
+ **Education** :
+ Bachelor's degree in **Biomedical Engineering** , **Electrical Engineering** , or a related technical discipline. A master's degree is a plus.
+ **Experience** :
+ **3+ years** of experience as a field engineer, preferably with **medical devices** or health technology systems.
+ **Proven experience** in installing, maintaining, and troubleshooting complex systems in a healthcare or clinical environment.
+ **Technical Skills** :
+ **Deep knowledge** of medical devices, system integrations, and technical protocols.
+ **Hands-on experience** with clinical equipment, including calibration, setup, and troubleshooting.
+ Proficient in **software troubleshooting** , system diagnostics, and firmware updates.
+ **Communication Skills** :
+ Strong written and verbal communication skills for **effective technical documentation** and **customer interaction** .
+ **Problem-Solving & Analytical Abilities** :
+ Strong **troubleshooting** and **problem-solving** skills
+ Capable of **data analysis** for system performance and creating actionable reports for improvements.
+ **Travel** :
+ Willing to travel extensively across **Europe** to hospital sites and patient homes, with a flexible schedule for support during system failure events.
**What is it like to work at Edwards Lifesciences in Germany?**
As a global leader in patient-focused medical innovations, we offer rewarding opportunities and exciting challenges in a truly international, dynamic and friendly work environment.
We are committed to fostering a diverse and inclusive work environment where all employees can grow, personally and professionally. To achieve this, we offer on-the-job development, training opportunities and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).
Edwards Lifesciences in Germany also offers the following benefits:
+ Competitive Compensation and Benefits package
+ Flexible working hours, remote working
+ Pension plan Risk
+ Insurance Meal Benefits
+ Service Awards Enhanced
+ Leave Benefits
+ Transportation Benefits
+ Employee Stock Purchase Programme
+ Employee Assistance Programme
+ Comprehensive Wellness Programme including onsite gym, yoga classes and massage, preventive health checks, healthy lifestyle webinars, educational events, charity activities and much more.
Benefits are regulated by an internal policy which contains the full details regarding the entitlement and conditions for the benefits. Benefits policy and components may vary by location.
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