28 Night Engineer jobs in Ireland
Quality Engineer 1 (Night Shift)
Galway, Connacht
Medtronic
Posted today
Job Viewed
Job Description
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
**Medtronic**
At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress and deliver meaningful innovations.
**Our Purpose**
At our Quality Department in Medtronic, plc, we focus on supporting the product value stream to ensure that customer and patient needs are met every day. Our key focus is on delivering and maintaining a high level of Quality to ensure that business and performance goals are achieved. The Quality Engineer role is critical in supporting key department metrics thus contributing to the global strategy and to deliver on our mission to contribute to human welfare by supporting the manufacture of products that alleviate pain, restore health, and extend life.
**_Come for a job, stay for a career!_**
**A Day in The Life Of:**
+ Responsibilities may include the following and other duties may be assigned.
+ Develops, modifies, applies and maintains quality standards and protocols for processing materials into partially finished or finished materials product.
+ Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
+ Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
+ Work on non-conformance Investigations.
+ Ensures that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.
+ Contribute to continuous improvement activities to support the business.
+ May collaborate in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
+ Ensure compliance to all applicable department and site-wide procedures, and regulations. Support Internal and External audit preparation and activity which includes application and maintenance of quality standards for all activities associated.
**Key Skills & Experience**
+ Minimum of a bachelor's degree (Level 7 NFQ) in Engineering/Science or related discipline with a minimum of 1-year relevant direct Science/Engineering experience within medical device environment.
+ Strong interpersonal, communication and organizational skills.
+ Practical working knowledge of statistical data analysis, problem solving and quality improvement tools and techniques preferable.
+ Technical writing skills.
+ Ability to multi-task and to take initiative is essential.
+ Effective time management skills.
+ Builds and maintains positive relationships with others; shows respect and consideration for others.
**Medtronic offer a competitive salary and flexible Benefits Package**
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email
**A Day in the Life**
**Medtronic**
At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress and deliver meaningful innovations.
**Our Purpose**
At our Quality Department in Medtronic, plc, we focus on supporting the product value stream to ensure that customer and patient needs are met every day. Our key focus is on delivering and maintaining a high level of Quality to ensure that business and performance goals are achieved. The Quality Engineer role is critical in supporting key department metrics thus contributing to the global strategy and to deliver on our mission to contribute to human welfare by supporting the manufacture of products that alleviate pain, restore health, and extend life.
**_Come for a job, stay for a career!_**
**A Day in The Life Of:**
+ Responsibilities may include the following and other duties may be assigned.
+ Develops, modifies, applies and maintains quality standards and protocols for processing materials into partially finished or finished materials product.
+ Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
+ Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
+ Work on non-conformance Investigations.
+ Ensures that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.
+ Contribute to continuous improvement activities to support the business.
+ May collaborate in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
+ Ensure compliance to all applicable department and site-wide procedures, and regulations. Support Internal and External audit preparation and activity which includes application and maintenance of quality standards for all activities associated.
**Key Skills & Experience**
+ Minimum of a bachelor's degree (Level 7 NFQ) in Engineering/Science or related discipline with a minimum of 1-year relevant direct Science/Engineering experience within medical device environment.
+ Strong interpersonal, communication and organizational skills.
+ Practical working knowledge of statistical data analysis, problem solving and quality improvement tools and techniques preferable.
+ Technical writing skills.
+ Ability to multi-task and to take initiative is essential.
+ Effective time management skills.
+ Builds and maintains positive relationships with others; shows respect and consideration for others.
**Medtronic offer a competitive salary and flexible Benefits Package**
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email
This advertiser has chosen not to accept applicants from your region.
0
Shift Quality Engineer
Dún Laoghaire, Leinster
embecta
Posted today
Job Viewed
Job Description
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. For more information, visit embecta.com or follow our social channels on LinkedIn , Facebook , Instagram and X ( .
**Why join us?**
A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees.
In this role the Shift Quality Engineer ensures quality engineering support for daily manufacturing operations, collaborating with the Quality Engineering team and Shift QC Leads to meet business quality standards.
The position follows a 7am-7pm schedule on a 4-day rotating basis, with occasional night shift coverage as needed.
+ Managing the activities of the Quality Inspectors to ensure optimal efficiency and compliance with all regulatory requirements.
+ Drive root cause analysis of non-conformances with relevant personnel and ensure corrections are implemented before starting back to production after a quality issue.
+ Drive and maintain cGMP practices across all operational departments under your quality responsibility (Incoming, moulding, assembly, packaging sterilization, warehouse) and attend departmental and other meetings as appropriate.
+ Preparation of relevant work sheets and execution of final inspection tests and line clearance verification.
+ Release batches in SAP from packaging to sterilization and final release.
+ Complete DHR reviews and batch releases.
+ Provide GMP guidance in case of rework and/or inspection protocols.
+ Line clearance verification.
+ Complete Product Quality Testing
+ Ensure that maintenance records and process adjustments records are maintained and captured in real time.
+ Ensure all CAPAs under your responsibility are completed in compliance with all regulatory and procedural commitments.
+ Participate in the Change Control Process.
+ Liaise with relevant personnel regarding flow of product through QC department and other issues that arise
+ Preparation, review and approval of technical documentation.
+ Manage and provide support with ongoing changes and continuous improvement projects
+ Perform training as required
+ Ensure the smooth running of functions under your control
+ Review, analyze and report on relevant customer complaints and institute corrective actions
+ Any other reasonable duties which may be required by management from time to time
**Educational Requirements:**
+ Third level qualification in a Science/Engineering discipline
**Relevant Experience:**
+ Strong knowledge and application ISO 9001/2000 or ISO 13485 environment.
+ Demonstrable experience in the preparation of Technical Documentation.
+ Understanding of Statistical Process Control and sampling techniques and standards
+ Experience with SAP and Trackwise is beneficial
+ Good experience in CAPA system management, incident report and MRB
+ Working knowledge of general validation activities
+ Experience in complaints analysis and reporting
+ A working knowledge of FDA requirements and managing FDA audits.
+ Proven ability of working in a cross-functional team environment.
+ Excellent interpersonal and communication skills.
+ High level of computer literacy.
embecta 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.
**Why join us?**
A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees.
In this role the Shift Quality Engineer ensures quality engineering support for daily manufacturing operations, collaborating with the Quality Engineering team and Shift QC Leads to meet business quality standards.
The position follows a 7am-7pm schedule on a 4-day rotating basis, with occasional night shift coverage as needed.
+ Managing the activities of the Quality Inspectors to ensure optimal efficiency and compliance with all regulatory requirements.
+ Drive root cause analysis of non-conformances with relevant personnel and ensure corrections are implemented before starting back to production after a quality issue.
+ Drive and maintain cGMP practices across all operational departments under your quality responsibility (Incoming, moulding, assembly, packaging sterilization, warehouse) and attend departmental and other meetings as appropriate.
+ Preparation of relevant work sheets and execution of final inspection tests and line clearance verification.
+ Release batches in SAP from packaging to sterilization and final release.
+ Complete DHR reviews and batch releases.
+ Provide GMP guidance in case of rework and/or inspection protocols.
+ Line clearance verification.
+ Complete Product Quality Testing
+ Ensure that maintenance records and process adjustments records are maintained and captured in real time.
+ Ensure all CAPAs under your responsibility are completed in compliance with all regulatory and procedural commitments.
+ Participate in the Change Control Process.
+ Liaise with relevant personnel regarding flow of product through QC department and other issues that arise
+ Preparation, review and approval of technical documentation.
+ Manage and provide support with ongoing changes and continuous improvement projects
+ Perform training as required
+ Ensure the smooth running of functions under your control
+ Review, analyze and report on relevant customer complaints and institute corrective actions
+ Any other reasonable duties which may be required by management from time to time
**Educational Requirements:**
+ Third level qualification in a Science/Engineering discipline
**Relevant Experience:**
+ Strong knowledge and application ISO 9001/2000 or ISO 13485 environment.
+ Demonstrable experience in the preparation of Technical Documentation.
+ Understanding of Statistical Process Control and sampling techniques and standards
+ Experience with SAP and Trackwise is beneficial
+ Good experience in CAPA system management, incident report and MRB
+ Working knowledge of general validation activities
+ Experience in complaints analysis and reporting
+ A working knowledge of FDA requirements and managing FDA audits.
+ Proven ability of working in a cross-functional team environment.
+ Excellent interpersonal and communication skills.
+ High level of computer literacy.
embecta 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.
This advertiser has chosen not to accept applicants from your region.
1
Maintenance Engineer
Dublin, Leinster
WM
Posted today
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
Maintenance Engineer
Cork, Munster
PM Group
Posted today
Job Viewed
Job Description
Overview The Outsourced Technical Services (OTS) Department at PM Group partners with Global leaders across a range of industries to find the best people for their current and ongoing business needs. Partnering with PM Group and our clients means that you will gain unrivalled experience working with global brands. We are currently recruiting an Maintenance Engineer who will be responsible for providing technical support to the maintenance, operations and project departments on equipment maintenance and reliability matters for pharmaceutical client in Cork. The Maintenance Engineer. Responsibilities Monitor day to day performance of systems. Troubleshooting of performance trends. Anticipating, solving or escalating problems as appropriate. Perform maintenance and improvement work on all equipment in order to enable full operations schedule adherence. Support the Preventative Maintenance program by carrying out effective maintenance routines and repairs to prolong the useful life and optimise the efficiency of equipment. Support of new product introductions and introduction of new equipment Responsible and accountable for the safe accomplishment of activities to all statutory, environmental, regulatory (cGMP), corporate site and department practices and procedures. Inputting into equipment design, construction, commissioning and qualification activities. Providing technical assistance to maintenance personnel and other departments as required. Developing maintenance procedures and equipment files. Assisting with generation, review and revision of maintenance documentation as necessary. Developing and managing the critical equipment list. Analyzing equipment data to report on equipment performance. Developing, Standardising and Implementing the latest maintenance approaches and techniques Developing a root cause failure analysis system. Engineering out re-occuring equipment problems. Supporting investigation and resolution of problems. Be familiar with daily activities in all areas of Maintenance department. Deputize for Maintenance Manager as necessary. Rotate with other positions in the department, as required. Facilitate an environment of continuous improvement. Lead investigations in work area as necessary. Interface with Manufacturing department (Supervisor, Manager and Director level). Contact with Quality, Logistics and Training departments Qualifications A Degree in Mechanical, Electrical, Instrumentation or Process Engineering. Reliability and/or Maintenance experience within a process or pharmaceutical cGMP regulated environment. Experience of best practices in preventive maintenance, condition monitoring, maintenance planning, reliability engineering, RCM or FMECA. Experience of Delta V, PLC, SCADA and SAP systems
This advertiser has chosen not to accept applicants from your region.
3
Maintenance Engineer Student
Wicklow, Leinster
Takeda Pharmaceuticals
Posted today
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Maintenance Engineer Student_**
This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Bray. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development. To support and contribute to activities in the Maintenance Department, Technical Services. This brief demands flexibility and cross-functional liaison and co-operation, combined with competent technical ability.
**_How you will contribute:_**
+ Work with flexibility within the Maintenance Department and in co-operation with other Departments.
+ Contribute to LEAN maintenance best practices within a continuous improvement environment.
+ Assist in developing and improving new and existing maintenance routines within a cGMP environment, using the sites computerised maintenance management system.
+ Assist in developing a digital mobile platform for the companies CMMS system and developing bar-coding for assets/spare parts.
+ Practical support of planning, execution and review of the site's annual maintenance shutdown event.
+ Regular reporting of activities to direct line manager and working closely with same to achieve targets / objectives throughout the internship
+ Develop and maintain a strong working relationship with all the departments' customers both internally and across the site.
In this position you will report to the **Maintenance Planner.**
**_What you bring to Takeda_** **:**
+ Excellent spoken and written English is essential.
+ Excellent communication and interpersonal skills.
+ Strong organizational skills. Drive and promote the corporate values of Takeda-ism within the workplace.
+ Ensure timely completion of all SOPs, reading, training and assessment.
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Previous experience in an engineering role is advantageous
**What Takeda can offer you:**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**More about us:**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**How we will support you:**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Maintenance Engineer Student_**
This role offers a unique opportunity to gain hands-on experience with cutting-edge analytical techniques in a dynamic, supportive team at Takeda's world-class facilities in Bray. Join us to develop your skills, contribute to life-changing medicines, and grow your career in an environment that values innovation, safety, and personal development. To support and contribute to activities in the Maintenance Department, Technical Services. This brief demands flexibility and cross-functional liaison and co-operation, combined with competent technical ability.
**_How you will contribute:_**
+ Work with flexibility within the Maintenance Department and in co-operation with other Departments.
+ Contribute to LEAN maintenance best practices within a continuous improvement environment.
+ Assist in developing and improving new and existing maintenance routines within a cGMP environment, using the sites computerised maintenance management system.
+ Assist in developing a digital mobile platform for the companies CMMS system and developing bar-coding for assets/spare parts.
+ Practical support of planning, execution and review of the site's annual maintenance shutdown event.
+ Regular reporting of activities to direct line manager and working closely with same to achieve targets / objectives throughout the internship
+ Develop and maintain a strong working relationship with all the departments' customers both internally and across the site.
In this position you will report to the **Maintenance Planner.**
**_What you bring to Takeda_** **:**
+ Excellent spoken and written English is essential.
+ Excellent communication and interpersonal skills.
+ Strong organizational skills. Drive and promote the corporate values of Takeda-ism within the workplace.
+ Ensure timely completion of all SOPs, reading, training and assessment.
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Previous experience in an engineering role is advantageous
**What Takeda can offer you:**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**More about us:**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**How we will support you:**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
4
Facilities Maintenance Engineer
Ballina, Connacht
Gertek Project Management
Posted today
Job Viewed
Job Description
About GerTEK: GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & have multiple projects that we support. We're looking for a hands-on and proactive Facilities Engineer to join our team! In this role, you'll be the go-to person for keeping our building's systems and infrastructure running smoothly. You'll ensure our facility is safe, efficient, and well-maintained, playing a vital part in our company's daily success. If you're a problem-solver with a strong technical background, we'd love to meet you. Key Responsibilities System Maintenance: Oversee the operation and maintenance of key building systems, including HVAC, electrical distribution, plumbing, and life safety systems. Preventative Maintenance: Develop and manage a preventative maintenance (PM) schedule to minimise downtime and ensure equipment reliability. Project Management: Manage small to medium-sized facilities projects, from system upgrades and equipment installations to office reconfigurations. Vendor Coordination: Liaise with and manage external contractors and service providers for specialised maintenance and repair work. Compliance & Safety: Ensure the facility complies with all health, safety (EHS), and environmental regulations. Qualifications & Skills A degree (Level 7 or 8) in Mechanical, Electrical, or Facilities Engineering, or a related technical field. 3+ years of experience in a facilities engineering or maintenance role, preferably in a manufacturing, corporate, or industrial environment. Strong technical knowledge of mechanical and electrical (M&E) systems. Experience with building management systems (BMS) is a plus. Excellent troubleshooting skills and a proactive approach to problem-solving. Strong organisational and communication skills. To start the process click the Continue to Application or Login/Register to apply button below.
This advertiser has chosen not to accept applicants from your region.
5
Electrical Maintenance Engineer
Limerick, Munster
Vickerstock UK
Posted today
Job Viewed
Job Description
Job description: Responsibilities: Work with Site Maintenance Managers, Planners and API Maintenance Lead on execution of the site maintenance program to deliver compliant, reliable and efficient operation of all plant and equipment. Support the Reliability Engineer in the execution of Reliability Centered Maintenance initiatives. Develop and lead a Root Cause Failure Analysis Program to reduce general equipment breakdowns and support maintenance personnel to conduct real time Root Cause Analysis. Work with the Reliability Engineer & Planning to establish and use reliability & work planning metrics/KPI's to monitor improvement and resource optimization e.g. PM/CM ratio, schedule adherence, etc. To carry out start up checks on machinery throughout the plant on a daily basis. Ensure that all breakdowns are carried out swiftly and safely at all times. Ensure that all servicing and maintenance throughout the site is done in an efficient, safe and hygienic manner. Smooth running of the factory. Repairs, servicing and good maintenance of machinery. Work on refrigeration, plumbing and all breakdowns is carried out in a safe and tidy manner. To implement and follow the preventative maintenance schedule To ensure that records are completed. Other duties as assigned. Refrigeration experience an advantage but not essential To ensure that the staff comply with the Company Health & Safety policy. The above job description is designed to give an appreciation of the main functions of the job. It is not intended to be exclusive or exhaustive. Qualifications Completion of a 4 year approved technical training program in mechanical or electrical repair and maintenance and 2 years electrical/mechanical experience; Or, Any equivalent combination of experience and/or education from which comparable knowledge, skills and abilities have been achieved including third and fourth year apprentices. Leaving Cert, School Diploma or Equivalent. Experience in a fast paced manufacturing environment Good communication and interpersonal skills, with the ability to take direction Ability to work well in a team Ability to challenge others in a professional and constructive manner Knowledge and experience in a food manufacturing environment an advantage, but not essential Skills: Electrical Maintenance Maintenance Management Site Management Engineering Troubleshooting
This advertiser has chosen not to accept applicants from your region.
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About the latest Night engineer Jobs in Ireland !
6
Electrical maintenance engineer
Limerick, Munster
Vickerstock UK
Posted today
Job Viewed
Job Description
A Large manufacturing company based in Limerick ROI is looking to employ and experienced Electrical Maintenance engineer Work with Site Maintenance Managers, Planners and API Maintenance Lead on execution of the site maintenance program to deliver compliant, reliable and efficient operation of all plant and equipment.
Support the Reliability Engineer in the execution of Reliability Centered Maintenance initiatives.
Develop and lead a Root Cause Failure Analysis Program to reduce general equipment breakdowns and support maintenance personnel to conduct real time Root Cause Analysis.
Work with the Reliability Engineer & Planning to establish and use reliability & work planning metrics/KPI's to monitor improvement and resource optimization e.g.
PM/CM ratio, schedule adherence, etc.
To carry out start up checks on machinery throughout the plant on a daily basis.
Ensure that all breakdowns are carried out swiftly and safely at all times.
Ensure that all servicing and maintenance throughout the site is done in an efficient, safe and hygienic manner.
Smooth running of the factory.
Repairs, servicing and good maintenance of machinery.
Work on refrigeration, plumbing and all breakdowns is carried out in a safe and tidy manner.
To implement and follow the preventative maintenance schedule To ensure that records are completed.
Other duties as assigned.
Refrigeration experience an advantage but not essential To ensure that the staff comply with the Company Health & Safety policy.
The above job description is designed to give an appreciation of the main functions of the job.
It is not intended to be exclusive or exhaustive.
Non Negotiables Must have previous Electrical Maintenace experience - Manufacturing Must live and eligible to work in the republic of Ireland Completion of a 4 year approved technical training program in mechanical or electrical repair and maintenance and 2 years electrical/mechanical experience; Or, Any equivalent combination of experience and/or education from which comparable knowledge, skills and abilities have been achieved including third and fourth year apprentices.
Leaving Cert, School Diploma or Equivalent.
Skills: Electrical Electrical Engineering Maintenance Maintenance Management
Support the Reliability Engineer in the execution of Reliability Centered Maintenance initiatives.
Develop and lead a Root Cause Failure Analysis Program to reduce general equipment breakdowns and support maintenance personnel to conduct real time Root Cause Analysis.
Work with the Reliability Engineer & Planning to establish and use reliability & work planning metrics/KPI's to monitor improvement and resource optimization e.g.
PM/CM ratio, schedule adherence, etc.
To carry out start up checks on machinery throughout the plant on a daily basis.
Ensure that all breakdowns are carried out swiftly and safely at all times.
Ensure that all servicing and maintenance throughout the site is done in an efficient, safe and hygienic manner.
Smooth running of the factory.
Repairs, servicing and good maintenance of machinery.
Work on refrigeration, plumbing and all breakdowns is carried out in a safe and tidy manner.
To implement and follow the preventative maintenance schedule To ensure that records are completed.
Other duties as assigned.
Refrigeration experience an advantage but not essential To ensure that the staff comply with the Company Health & Safety policy.
The above job description is designed to give an appreciation of the main functions of the job.
It is not intended to be exclusive or exhaustive.
Non Negotiables Must have previous Electrical Maintenace experience - Manufacturing Must live and eligible to work in the republic of Ireland Completion of a 4 year approved technical training program in mechanical or electrical repair and maintenance and 2 years electrical/mechanical experience; Or, Any equivalent combination of experience and/or education from which comparable knowledge, skills and abilities have been achieved including third and fourth year apprentices.
Leaving Cert, School Diploma or Equivalent.
Skills: Electrical Electrical Engineering Maintenance Maintenance Management
This advertiser has chosen not to accept applicants from your region.
7
Facilities maintenance engineer
Mayo, Connacht
Gertek Project Management
Posted today
Job Viewed
Job Description
About Ger TEK: Ger TEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services.
We partner with many of the world's largest life science & have multiple projects that we support.
We're looking for a hands-on and proactive Facilities Engineer to join our team! In this role, you'll be the go-to person for keeping our building's systems and infrastructure running smoothly.
You'll ensure our facility is safe, efficient, and well-maintained, playing a vital part in our company's daily success.
If you're a problem-solver with a strong technical background, we'd love to meet you.
Key Responsibilities System Maintenance: Oversee the operation and maintenance of key building systems, including HVAC, electrical distribution, plumbing, and life safety systems.
Preventative Maintenance: Develop and manage a preventative maintenance (PM) schedule to minimise downtime and ensure equipment reliability.
Project Management: Manage small to medium-sized facilities projects, from system upgrades and equipment installations to office reconfigurations.
Vendor Coordination: Liaise with and manage external contractors and service providers for specialised maintenance and repair work.
Compliance & Safety: Ensure the facility complies with all health, safety (EHS), and environmental regulations.
Qualifications & Skills A degree (Level 7 or 8) in Mechanical, Electrical, or Facilities Engineering, or a related technical field.
3+ years of experience in a facilities engineering or maintenance role, preferably in a manufacturing, corporate, or industrial environment.
Strong technical knowledge of mechanical and electrical (M&E) systems.
Experience with building management systems (BMS) is a plus.
Excellent troubleshooting skills and a proactive approach to problem-solving.
Strong organisational and communication skills.
To start the process click the Continue to Application or Login/Register to apply button below.
We partner with many of the world's largest life science & have multiple projects that we support.
We're looking for a hands-on and proactive Facilities Engineer to join our team! In this role, you'll be the go-to person for keeping our building's systems and infrastructure running smoothly.
You'll ensure our facility is safe, efficient, and well-maintained, playing a vital part in our company's daily success.
If you're a problem-solver with a strong technical background, we'd love to meet you.
Key Responsibilities System Maintenance: Oversee the operation and maintenance of key building systems, including HVAC, electrical distribution, plumbing, and life safety systems.
Preventative Maintenance: Develop and manage a preventative maintenance (PM) schedule to minimise downtime and ensure equipment reliability.
Project Management: Manage small to medium-sized facilities projects, from system upgrades and equipment installations to office reconfigurations.
Vendor Coordination: Liaise with and manage external contractors and service providers for specialised maintenance and repair work.
Compliance & Safety: Ensure the facility complies with all health, safety (EHS), and environmental regulations.
Qualifications & Skills A degree (Level 7 or 8) in Mechanical, Electrical, or Facilities Engineering, or a related technical field.
3+ years of experience in a facilities engineering or maintenance role, preferably in a manufacturing, corporate, or industrial environment.
Strong technical knowledge of mechanical and electrical (M&E) systems.
Experience with building management systems (BMS) is a plus.
Excellent troubleshooting skills and a proactive approach to problem-solving.
Strong organisational and communication skills.
To start the process click the Continue to Application or Login/Register to apply button below.
This advertiser has chosen not to accept applicants from your region.
8
Operations Quality Engineer Shift
Kilkenny, Leinster
Abbott
Posted today
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.
**This is how you can make a difference at Abbott:**
As an Operations Quality Engineer you will Analyse quality standards for components, materials or services. Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. Provide Quality expertise and guidance to Manufacturing/Operations, Technical/Product Test and Incoming Materials to support the manufacture and delivery of quality and compliant products on time, in full and cost effectively to meet the needs of the business and customers.
This is a shift based role on 4 cycle shift.
**Responsibilities:**
+ Apply quality principles, analyses quality records, prepares reports and recommends improvements.
+ Conduct inspection, verification and validation of components or materials used in development processes.
+ Identify and address recurring problems either with the quality of the product or the reliability of testing procedures.
+ Document quality issues and performance measures for management review.
+ May liaise with external vendors.
+ Monitor and maintain the validation status of site products, processes and systems and monitor and maintain process FMEA and Critical Quality Attribute systems. Maintain site validation plans and periodic review process. Support Equipment and Software validation activities and support Process validation activities
+ Provide regular updates to peers and colleagues on project resource requirements and ensure other quality functions are brought into project teams at appropriate points.
+ Report on and support the implementation of actions to reduce the occurrence/reoccurrence of non-conformances within Manufacturing, Product Test and Incoming Material and initiating Exception Reports for discrepancies observed during inspection / testing & review activities.
+ Present and communicate status, report metrics, identify trends potential issues, improvement initiatives and CAPA requirements.
+ Investigating customer complaints and forwarding reports to PQA group and responsible for maintaining Corrective and Preventive Action programs.
+ Responsible for maintaining an appropriate balance of quality, compliance and business risk and responsible for ensuring teams use appropriate risk management tools to prioritize certain activities and justify the level of effort required.
+ Monitor and maintain the quality and compliance status of associated quality records and ensure project teams maintain project records in compliance with Quality System and planned requirements.
+ Support DMR change control and calibration activities.
**Qualifications and Experience**
+ Minimum NFQ Level 7 Qualification in Engineering or Manufacturing qualification
+ 3 years in a Manufacturing / Science or Engineering environment
+ GMP/GDP experience
+ ISO 13485 experience
+ Yellow belt qualification desired.
**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
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.
**This is how you can make a difference at Abbott:**
As an Operations Quality Engineer you will Analyse quality standards for components, materials or services. Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. Provide Quality expertise and guidance to Manufacturing/Operations, Technical/Product Test and Incoming Materials to support the manufacture and delivery of quality and compliant products on time, in full and cost effectively to meet the needs of the business and customers.
This is a shift based role on 4 cycle shift.
**Responsibilities:**
+ Apply quality principles, analyses quality records, prepares reports and recommends improvements.
+ Conduct inspection, verification and validation of components or materials used in development processes.
+ Identify and address recurring problems either with the quality of the product or the reliability of testing procedures.
+ Document quality issues and performance measures for management review.
+ May liaise with external vendors.
+ Monitor and maintain the validation status of site products, processes and systems and monitor and maintain process FMEA and Critical Quality Attribute systems. Maintain site validation plans and periodic review process. Support Equipment and Software validation activities and support Process validation activities
+ Provide regular updates to peers and colleagues on project resource requirements and ensure other quality functions are brought into project teams at appropriate points.
+ Report on and support the implementation of actions to reduce the occurrence/reoccurrence of non-conformances within Manufacturing, Product Test and Incoming Material and initiating Exception Reports for discrepancies observed during inspection / testing & review activities.
+ Present and communicate status, report metrics, identify trends potential issues, improvement initiatives and CAPA requirements.
+ Investigating customer complaints and forwarding reports to PQA group and responsible for maintaining Corrective and Preventive Action programs.
+ Responsible for maintaining an appropriate balance of quality, compliance and business risk and responsible for ensuring teams use appropriate risk management tools to prioritize certain activities and justify the level of effort required.
+ Monitor and maintain the quality and compliance status of associated quality records and ensure project teams maintain project records in compliance with Quality System and planned requirements.
+ Support DMR change control and calibration activities.
**Qualifications and Experience**
+ Minimum NFQ Level 7 Qualification in Engineering or Manufacturing qualification
+ 3 years in a Manufacturing / Science or Engineering environment
+ GMP/GDP experience
+ ISO 13485 experience
+ Yellow belt qualification desired.
**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.
9