130 Equipment Engineer jobs in Ireland

Biologics Process Equipment Engineer We're seeking a Biologics Process Equipment Engineer to join our Engineering team. You'll be a Subject Matter Expert for vial filling and isolator equipment, supporting our pharmaceutical operations. What you'll do: Act as the SME for vial filling and isolator equipment, from design to handover. Lead FAT and SAT activities to ensure equipment meets technical requirements. Develop and execute commissioning plans and review validation protocols. Troubleshoot equipment malfunctions and support continuous improvement initiatives. Collaborate with internal and external teams to optimize equipment and process performance. What you'll bring: Degree in Engineering, Science, or a technical discipline. 5+ years of combined experience in Process, Equipment, or Manufacturing Engineering within a pharmaceutical or healthcare organization. 3+ years in a manufacturing environment (biotechnology, pharmaceutical, or healthcare). Experience with biotechnological or parenteral drug manufacturing, solutions preparation, and sterilization is a plus. Familiarity with new product introductions to pharmaceutical facilities is desirable. To start the process click the Continue to Application or Login/Register to apply button below.

Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. About Technical Operations BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. Senior Equipment Engineer/Equipment EngineerShanbally, Ringaskiddy, CorkOnsite RoleClosing Date: 25th August 2025Biologics Centre of Excellence(CoE), Technical Development Services (TDS) is hiring ahighly skilled and experiencedSenior Equipment Engineer/Equipment Engineerto oversee the management and maintenance of laboratory equipment. The ideal candidate will have a strong background in engineering, exceptional problem-solving skills, and a passion for ensuring the accuracy and reliability of lab instruments. Strategic thinking and the ability to align equipment management with the broader goals of the organization are essential. Key Responsibilities:This person will be responsible for the delivery and operational management of the lab asset management processes & systems. Design and implement the laboratory equipment asset system, along with their supporting lifecycle management processes. Manage and maintain all laboratory equipment, ensuring optimal performance and adherence to safety standards. Provide clear visibility of all laboratory equipment and their associated asset lifecycle costs. Diagnose and troubleshoot equipment/instrument technical issues, collaborating closely with vendors and service providers for repairs and replacements. Using Asset management principles to guide specification of KPI's for Lab Operations program. Deliver dashboard(s) that provide clear performance reporting for each type of lab asset Will be a prominent change leader for new processes interacting with both internal & external vendors, global procurement, and scientific functions. Partner with Automation and IT to align data consistency & reporting relating to lab equipment assets. Apply standard data analysis practices and techniques to establish root cause for product and process failures or to support the justification for improvements to products and processes. Contribute to the strategic planning of laboratory operations, aligning equipment management with the organization's long-term objectives. Review procedures and CAPEX equipment plans prior to implementation as well as existing ones for failure analysis and potential improvements. Oversee equipment asset lifecycle management, ensuring timely preventive maintenance and accurate repair documentation in the Computerized Maintenance Management System. Strong fault-finding expertise to identify faults or issues with lab equipment to ensure quick turnaround of equipment for maximum uptime. Coordinate and/or conduct training sessions for laboratory personnel on the proper use and care of equipment. Stay informed about the latest advancements in laboratory technology and recommend upgrades as necessary. Work in partnership with Engineering Reliability Team to develop and maintain reliability program for lab equipment Develop FMEA's or similar for existing and new lab equipment to identify key objectives or priorities for asset life management Adhere to all safety, environmental, security and quality requirements including, but not limited to: Safety & Environmental Management Systems, Quality Management Systems (QMS) regulations, company policies and operating procedures, and other regulatory requirements. Facilitate or contribute to corrective and preventive actions while supporting the achievement of Biologics CoE SQDEC standards as well as 5S principles. Qualifications & Skills: Bachelor or Master's degree in engineering, preferably in Mechanical, Electrical, Chemical or Biomedical Engineering. Minimum of 5 years of experience in lab equipment management or a related field. Experience of Reliability programs and management Proven expertise in the maintenance and repair of laboratory instruments. Strong strategic thinking abilities and experience in integrating equipment management with organizational goals. Proficient in the use of Excel, Power Point and Visio software. Familiar with basic Data analytics and statistical methods. Proficiency with CMMS & Power BI would be an advantage. Demonstrated results through Lean practices and principles. Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Continue to Application or Login/Register to apply button below.

Overview PM Group is an employee owned, international project delivery firm with a team of 3,600+ people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients and trade partners. Our Vision is to be a highly valued and creative delivery partner, building a more sustainable world with our clients. To do this our people are key and is where you can play a part. We currently have a requirement for a Mechanical Engineer/Equipment Package Engineer to work on various projects. This role will provide the successful applicant with the opportunity to further develop their technical and managerial skills along with excellent opportunities for career advancement. The role is based from our Cork office with hybrid working arrangements. Responsibilities As Mechanical Engineer/Equipment Package Engineer you would be responsible for:- Ownership of equipment modules and packages through design and procurement phases Generation of Data Sheets, Material Requisitions & Enquiry Packages for procurement of equipment Generation of Technical Bid Tab Evaluation of vendors in compliance with Client specifications Developing Technical Specifications in compliance with Client requirements Development of each package through Kick-off meetings, Design Reviews, FAT's etc. Project manage Suppliers to ensure packages are designed, manufactured and tested as per project requirements Interfacing with clients, vendors, client project management and other disciplines ensuring the highest level of service is provided Interfacing with client design team/end users Mechanical optimization/site support Delivery of agreed design scope within budget hours and schedule Qualifications To be considered for this role, you will have: Degree in Mechanical Engineering (Engineers with a primary degree in Chemical/Process Engineering and relevant process experience may also be considered) Some design experience in the Pharmaceutical and Biopharmaceutical sectors Self-starter with confidence in coordinating the efforts of others Good communication skills (ability to lead Technical reviews with Clients and Suppliers) Openness to travel to where equipment is being manufactured Why PM Group? As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy. Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future. Our benefits include: Flexible working arrangements , including a hybrid working policy An employee-owned share scheme . All employees have the opportunity to invest in the company, every one contributing to the success of the company Pension, bonus, educational assistance and many other benefits PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know. Attention Agencies/Search Firms/Third Party Recruiters: Please do not call or email to offer unsolicited resumes, CVs or Bios. PM Group does not require assistance from search firms, agencies or third party recruiters to recruit for employment opportunities or to fill vacancies within PM Group. In the absence of a written agreement setting out specifically negotiated terms and conditions regarding recruitment or placement in respect of one or more specific roles with PM Group and regardless of past practice, the submission of resumes, CVs or bios submitted by search firms, agencies or third party recruiters to any PM Group personnel whether via-email, through the PM Group website or presented directly to hiring managers at PM Group will not give rise to any fee or other entitlement to remuneration to be paid by PM Group in any circumstances. #LI-MC

Overview We are expanding our Mechanical Engineering team due to the ongoing demand that comes with new projects. In particular, we'd like to hear from Senior Mechanical Engineers. You will get the opportunity to work on a range of Pharmaceutical, Biopharmaceutical, Food and Beverage projects; from conceptual stage through to detailed design, commissioning and qualification. Based at our Cork office, you will have a hybrid work pattern. Responsibilities As a Senior Mechanical Engineer/Senior Equipment Package Engineer you will be responsible for:- Ownership of equipment modules and packages through design and procurement phases Generation of Data Sheets, Material Requisitions & Enquiry Packages for procurement of equipment Generation of Technical Bid Tab Evaluation of vendors in compliance with Client specifications Developing Technical Specifications in compliance with Client requirements Development of each package through Kick-off meetings, Design Reviews, FAT's etc. Project manage Suppliers to ensure packages are designed, manufactured and tested as per project requirements Interfacing with clients, vendors, client project management and other disciplines ensuring the highest level of service is provided Interfacing with client design team/end users Mechanical optimization/site support Delivery of agreed design scope within budget hours and schedule There is great scope for developing your skillset and enhancing your career. This can take the shape of becoming a Lead Mechanical Engineering on even larger projects or to become a Subject Matter Expert in your area. At PM Group, there is also the opportunity to mentor and coach junior team members in the Mechanical Department, many are on our award-winning Graduate Programme. Qualifications To be considered for this role, you will have: Degree in Mechanical Engineering (Engineers with a primary degree in Chemical/Process Engineering and relevant process experience may also be considered) Significant design experience in the Pharmaceutical and Biopharmaceutical sectors Self-starter with confidence in coordinating the efforts of others Good communication skills (ability to lead Technical reviews with Clients and Suppliers) Openness to travel to where equipment is being manufactured. Why PM Group? PM Group is an employee owned, international project delivery firm with a team of 3,600+ people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients and trade partners. Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future. Our benefits include: Flexible working arrangements , including a hybrid working policy An employee-owned share scheme . All employees have the opportunity to invest in the company, every one contributing to the success of the company Pension, bonus, educational assistance and many other benefits PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know. Attention Agencies/Search Firms/Third Party Recruiters: Please do not call or email to offer unsolicited resumes, CVs or Bios. PM Group does not require assistance from search firms, agencies or third party recruiters to recruit for employment opportunities or to fill vacancies within PM Group. In the absence of a written agreement setting out specifically negotiated terms and conditions regarding recruitment or placement in respect of one or more specific roles with PM Group and regardless of past practice, the submission of resumes, CVs or bios submitted by search firms, agencies or third party recruiters to any PM Group personnel whether via-email, through the PM Group website or presented directly to hiring managers at PM Group will not give rise to any fee or other entitlement to remuneration to be paid by PM Group in any circumstances. #LI-MC

**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.
**Key Responsibilities**
- Plans and conducts small- to medium-sized assigned projects within engineering specialty requiring conventional types of plans, investigations, and/or equipment validations.
- Maintains a good understanding of customer, business, and technical considerations, incorporating into work/project scoping and planning.
- Coordinates, monitors and manages activity/project implementation, adjusting as required to ensure quality and alignment to plan.
- Estimates and coordinates resources needed (materials, budget, time and people) to accomplish assigned tasks, incorporating contingencies
- Participates in basic economic analysis and feasibility studies related to project alternatives with support.
- Benchmarks and monitors external and internal environments, evaluating changes as potential indicators of future problems and/or opportunities, and preparing for those potential scenarios
- Independently executes the design of products/processes/equipment /systems/facilities using standard engineering theories, concepts, and techniques within the discipline.
- Independently investigates, conducts tests or experiments, gathers data, and performs preliminary analysis, reports findings and communicates recommendations to a variety of stakeholder audiences.
- Creates/modifies designs for intermediate problems, including designing and modifying more complex components/processes, and writing detailed design specifications.
- Reviews and analyzes data for patterns/trends, seeing relationships of growing complexity among the data, drawing insights and making recommendations to pursue opportunities and/or solve problems.
- Conducts root cause analysis to resolve underlying problems, applying a customer-centric lens to identify needs and propose solutions/alterations to meet those needs.
- Implements improvements to methods, designs and processes, proactively sharing and adopting ideas and best practices to reduce cost and optimize efficiencies/effectiveness
- Communicates to a variety of stakeholders using formal and informal media, based on the needs and priorities of the audience
- Builds open, honest, collaborative with a network of colleagues, contractors and vendors by developing an understanding of others' needs, promoting common goals, and following through on commitments.
- Mentors others by sharing technical expertise and providing feedback and guidance within the team and to cross-functional partners
**Minimum Experience Required**
Experience in GMP regulated environment
**Minimum Education Required**
A Bachelors Degree in Engineering, science or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 2+ years of significant engineering and/or operational experience. Additional post-graduate education may contribute towards the desired years of experience.
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

Job Description
**Have you ever wanted to make a difference?**
At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.
**Abbott Ireland**
In Ireland, Abbott employs over 5,000 people across nine sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**Diabetes Care Kilkenny**
Our new manufacturing facility in Kilkenny, opening in 2024, reflects the growing demand for Abbott's global Diabetes Care products. The facility will be a centre for world-class engineering, quality, medical device manufacturing, and other science-based professionals to produce life-changing technologies, including the FreeStyle Libre 3, a system that automatically delivers real-time, up-to-the-minute glucose readings, with the smallest and thinnest wearable glucose sensor that provides unsurpassed 14-day accuracy and optional glucose alarms directly to smartphones. This enables people with diabetes to live the best and fullest lives they can.
At Abbott in Kilkenny, you can shape your career as you help shape the future of healthcare.
**This is how you can make a difference at Abbott:**
In this role you will be in charge to apply subject matter knowledge in the area of Pharmaceutical/Biological Process. You will require capacity to apply skills/knowledge within the context of specific needs or requirements.
It will be a very big plus if you can bring experience in developing projects or sites from square one.
As Process Engineer, you will be responsible to:
+ Implement and maintain pharmaceutical/biological processes.
+ Calculate and organize all data for complex process flow sheets including instrumentation and control considerations.
+ Model processes and units operations.
+ Ensure proper sequence of operation and prepares specifications and operating instructions for processing equipment.
+ Conduct tests and measurements throughout stages of production to determine control over such variables as temperature, density, pressure and viscosity.
+ Service, troubleshoot and solve engineering problems with processes or equipment already in operation.
+ Ensure processes and procedures are in compliance with regulations.
+ May be responsible for corrective and preventive actions and investigation management.
**QUALIFICATIONS AND EXPERIENCE**
+ A relevant third level qualification in Engineering/Manufacturing/Science.
+ Minimum 2 years experience in the Engineering/Manufacturing/ Scientific field.
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

**Process Engineer**
+ _Location Waterford_
+ _24/7 Shift Pattern_
+ _Fixed Term Contract_
**About the Opportunity**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Your job, as Process Engineer, will be to provide support to the Pre filled syringe (PFS) & Multi Format Filling Line (MFFL) line for the aseptic processing of monoclonal antibody (mAb) commercial products. You will support business as usual operations for state of the art equipment, engineering test executions for projects and work as part of a highly focused and integrated Engineering Team in a Sterile Manufacturing environment.
Ready to get started?
**Main responsibilities:**
+ Shift pattern of 2 days, 2 nights (12 hour shift) followed by 4 days off.
+ Execute Process Engineering activities (cycle development protocol/reports, project improvements, deviations, problem solving, change controls, etc) to schedule and to the appropriate compliance and safety standards.
+ The main area of work would be on the Aseptic Syringe Filling Line which includes Debagger / Ebeam / Delid / Deline / Isolator / Syringe filling machine with multi filling technologies.
+ Supporting the day to day operation, data analysis and trending of parameters on equipment.
+ Provide engineering support to other areas of the PFS/ MFFL process such as Filling, Formulation, Autoclaving and Washing.
+ Provide technical support to implement process improvements, new product transfers to the site and production.
+ Support commercial manufacturing through delivery of key performance metrics (SQDCI).
**About you:**
+ Manufacturing engineering experience in a highly regulated GMP environment.
+ Degree in an Engineering discipline.
+ Strong problem-solving skills.
+ Strong documentation/protocol generation and execution skills.
+ Excellent communication skills.
+ Improvement resulting in on-going change.
+ Focused on achieving results.
+ Work well as a team member.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**Process Engineer**
+ _Location Waterford_
+ _Fixed Term Contract_
**About Waterford**
For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.
As Process Engineer you will be responsible for:
**Main responsibilities:**
+ Provide process engineering support to the Lyo APU.
+ Support delivery of continuous improvement projects to existing equipment.
+ Work closely with various departments, such as MSAT, Technical Development, Quality Assurance, and Supply Chain.
+ Lead and coordinate elements of an automated inspection project and contribute to process engineering activities related to the development of new and existing manufacturing capacity.
+ Utilisation of knowledge gained from existing manufacturing technologies to aid in the development of new technologies with the goal of implementing higher output and yield.
+ Ensure safety compliance, providing technical and engineering support for process and equipment failures, identifying, and implementing process and product improvements, supporting qualification of new products/processes, analysing machine performance data, and managing improvement projects within budget and time constraints.
+ Support new product introductions and capacity expansions, including new vendor selections, maintenance planning, design changes, change controls, OEE improvement, yield improvement, etc.
+ Lead systematic technical root cause investigations, Customer Complaints, Vendor Complaint, Change Controls and annual PQR Reports.
+ Support all company safety and quality programs and initiatives.
**About you**
+ Experience in a highly regulated GMP environment.
+ Degree in an Engineering discipline.
+ Strong problem solving and communication skills.
+ Strong documentation/protocol generation and execution skills.
+ Background in high volume inspection with demonstrated experience.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**Have you ever wanted to make a difference?**
At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.
**Abbott Ireland**
In Ireland, Abbott employs over 5,000 people across nine sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**Diabetes Care Kilkenny**
Our new manufacturing facility in Kilkenny, opening in 2024, reflects the growing demand for Abbott's global Diabetes Care products. The facility will be a centre for world-class engineering, quality, medical device manufacturing, and other science-based professionals to produce life-changing technologies, including the FreeStyle Libre 3, a system that automatically delivers real-time, up-to-the-minute glucose readings, with the smallest and thinnest wearable glucose sensor that provides unsurpassed 14-day accuracy and optional glucose alarms directly to smartphones. This enables people with diabetes to live the best and fullest lives they can.
At Abbott in Kilkenny, you can shape your career as you help shape the future of healthcare.
**This is how you can make a difference at Abbott:**
In this role you will be in charge to apply subject matter knowledge in the area of Pharmaceutical/Biological Process. You will require capacity to apply skills/knowledge within the context of specific needs or requirements.
It will be a very big plus if you can bring experience in developing projects or sites from square one.
As Process Engineer, you will be responsible to:
+ Implement and maintain pharmaceutical/biological processes.
+ Calculate and organize all data for complex process flow sheets including instrumentation and control considerations.
+ Model processes and units operations.
+ Ensure proper sequence of operation and prepares specifications and operating instructions for processing equipment.
+ Conduct tests and measurements throughout stages of production to determine control over such variables as temperature, density, pressure and viscosity.
+ Service, troubleshoot and solve engineering problems with processes or equipment already in operation.
+ Ensure processes and procedures are in compliance with regulations.
+ May be responsible for corrective and preventive actions and investigation management.
**QUALIFICATIONS AND EXPERIENCE**
+ A relevant third level qualification in Engineering/Manufacturing/Science.
+ Minimum 2 years experience in the Engineering/Manufacturing/ Scientific field.
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