126 Process Engineer jobs in Ireland

Are you a process or manufacturing engineer looking to progress your career? Are you interested in taking the next step in your professional journey with a global leader in the medical device industry? Are you familiar with remediation tasks? Are you ready to challenge yourself in a fast-paced and high-regulated environment? You could be the perfect candidate for this opportunity! Don't hesitate, apply today! Job Description Our client in Cork require experienced Process Engineers to support an upcoming project. This role will focus on manufacturing process validation, quality system updates, and documentation remediation. You will be based onsite and work directly with manufacturing and quality process owners to identify compliance gaps, implement corrective actions, and ensure documentation is accurate and audit-ready. Key ResponsibilitiesAnalyse process, product, material or equipment specifications and performance requirementsUnder broad supervision / guidance compile and analyse operational, test and experimental data to establish performance standards for newly implemented or modified products / processesSummarise, analyse and draw conclusions from test results leading to effective technical resolutionTroubleshoot new products / process working closely with product developmentContinually seek to drive / improvements in process design, layout and operational performanceDemonstrate good working knowledge and application of validation techniques and associated regulatory requirementsActively promotes and participates in a cross -functional teamwork environmentEvaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effectsUnderstands and comply with all the regulations governing the quality systems Key RequirementsEngineering or Quality degree with 2-3 years' relevant industry experienceBackground in remediation, process validation, CAPA, NCRs.Strong technical writing and documentation skills.Knowledge of 21 CFR Part 820, ISO 13485. BenefitsCompetitive and attractive employee compensation packagePension contributionsHealth insurancePaid public holidays Location: Cork, Ireland | onsite

**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.
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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 ABOUT ITW MEDICAL: Founded in 1912, Illinois Tool Works Inc. (NYSE: ITW) is a diversified, Fortune 200 manufacturing company that delivers specialized expertise, innovative thinking, and value-added products to meet critical customer needs in a variety of industries. Ranked among Fortunes Magazines most admired companies, the company focuses on solid growth, improving profitability and strong returns across its worldwide platforms and divisions. These divisions serve customers and markets around the globe, with a significant presence in developed as well as emerging markets. ITWs revenues totalled $12.6 billion in 2020. ITW Medical is comprised of two highly-respected medical product brands - Coeur & Filtertek supplying medical devices and components to global medical device brands. Filtertek manufactures moulded filtration and flow control components. Coeur is a leading provider of disposable diagnostic imaging consumables. General Accountability: Reporting to the Manufacturing Engineering Manager, the ProcessEngineeris responsible for providing engineering support. Responsibilities include the initial development of manufacturing processes for new products and providing technical expertise for troubleshooting current manufacturing processes. The candidate should have mechanical / manufacturing aptitude manufacturing process development. Typical manufacturing processes include Ultra sonic welding, and other automated processes. Duties and Responsibilities: Complete process development and testing through the use of a systematic process, employing Design of Experiments (DOEs) and other relevant techniques to achieve optimum manufacturing processes. Provide input to process specifications, equipment specifications, request for quotations, factory/site acceptance plans, engineering processes, etc. Provides technical consultation and support to New Product Development or Operations, regarding product designs and manufacturing process parameters and specifications. Using process expertise must be able to input into initial new product designs for Design for Manufacturability, Assembly and Cost. Specifies and/or designs/details proof of concept equipment, components or tooling as required to meet project assignments. Conduct process/equipment troubleshooting and root cause analysis. Ability to work closely with plant engineers, operators, and maintenance to troubleshoot machine and/or process issues and to provide training and mentoring to broaden their skills. Lead or coordinate the design and testing of pilot or mock-up processes for proof-of-concept work. Coordinate and conduct validations (IQ, OQ, PQ) Develop and implement work instructions and standardization of processes. Comply with OSHA Safety and Health regulations, along with other federal, state, and local regulations regarding environmental, industrial, and electrical mandates. May provide direction and training to entry level engineers and technicians to strengthen skill sets and assist in the talent development activities to ensure a strong pipeline of engineering talent. Qualifications: Bachelors Degree in Engineering (Manufacturing, Plastics, Biomedical or Mechanical) required. A minimum of 3+ years related work experience in a Process Engineering type role in a high-volume manufacturing environment required. Experience with medical device manufacturing is strongly preferred. Must be able to manage strategic manufacturing projects in a broad range of technologies. Ability to read and understand complex instructions such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to apply problem solving techniques to make independent decisions and suggestions on ways to improve services and processes and address complex issues. Independent and organized work style: effectively manage time and prioritize workload, adapt to change, and consistently meet deadlines Ability to carry out detailed, complex oral or written instructions Proven business aptitude, must be a decision-maker, willing to take calculated risks and can take advantage of business opportunities as they arise Possess ability to forge strong working relationships and successfully interact with operational functions, business areas, external partners, employees, and senior management Excellent written and verbal communication skills and good listening skills Computer experience is preferred with knowledge of Microsoft office. AutoCAD or other drafting software experience is preferred Novice electrical and mechanical knowledge needed Physical Requirements: Work may be performed in an office or manufacturing/cleanroom environment Must be able to stand, walk, bend, stoop, or climb for extended periods of time Must be able to lift 20-50 lbs.

LSC have a great contract opportunity for a Process Engineer to join a global Biopharmaceutical company in Carlow. This is a state-of-the-art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia, and infectious disease. ABOUT THE PROJECT - KEY RESPONSIBILITIES: Design/Author/Review/Approve/Execute qualification/validation documentation and process development studies in line with the standard approval process Design/Author/Review/Approve/Execution/development of change controls Contribution to Kaizen events as appropriate Technical input into quality notification by authoring/reviewing/approving investigations Execution of equipment/qualification validation programs; including re-qualification and re-validation Support continuous improvement through Lean Six Sigma methodologies ABOUT YOU - ARE YOUR SKILLS A MATCH? Bachelor's Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline Min 3 years' experience ideally in manufacturing, preferably GMP Setting Demonstratable experience of leading technical related projects Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply! Apply via this advert or contact Adam Murphy at if you have any more questions about this opportunity!

Job title:Process Engineer Location:Dublin 15 Benefits:Excellent hourly rate Company: My client are a global specialty pharmaceutical and medical device company dedicated to improving patient health through innovative therapies and technologies. Their Blanchardstown campus in Dublin serves as a key hub for advanced manufacturing and global R&D, delivering high-quality medical devices to patients worldwide. With a strong commitment to operational excellence, regulatory compliance, and continuous innovation, my client offer an inclusive, collaborative work environment where employees can make a real impact. Duties & Responsibilities include but are not limited to: The position requires effective cross-functional collaboration with internal partners including Site Engineering, Facilities Management, Manufacturing Operations, Technical Operations, and Quality and external contractors. Manage all process engineering activities and utility activities to meet and optimize manufacturing schedules while maintaining a high level of GMP compliance and cost efficiency. Manage process engineering activities includes all planned and unplanned works on process equipment. Coordinates with maintenance all utilities equipment activities including all planned and unplanned works on utility equipment associated with the clean areas. In addition to vendor training provide training to the process and utility technicians on process equipment. Collaborate with the maintenance and utlities lead to optimise the preventative maintenance program across process and utility systems including a review of executed maintenance activities and identify improvements to the maintenance job plan content. Implement equipment and maintenance reliability improvements. Development and implementation of area / equipment improvement plans to repeat failures and other maintenance problems. Life cycle management of the validation of qualified equipment and ongoing process engineering support for this equipment. Provide support to Manufacturing, Validation, and Maintenance on process equipment and utility systems when required. Manage all process engineering and validation activities associated with qualified equipment on site. Coordinate with quality and other areas on the requalification program. Manage vendors supporting/executing the works. Provide Engineering expertise in trouble shooting activities to support manufacturing during process transfer activities or deviation investigations. Provide support and participate in regulatory inspections. Lead and support system improvements, development of specifications, engineering documents and standard operating procedures. Identify and support process optimization initiatives and address opportunities for efficiency and capacity improvements in all areas of manufacturing support equipment. Education & Experience Required : A third level degree in Process Engineering or equivalent experience Relevant experience working in a technical engineering role in the Pharmaceutical / Biotechnology industry. Evidence of continuous professional development. Team leadership experience. Experienced in identifying priorities for assignment of resources and time. Experienced in the application of lean principles and structured problem-solving techniques. Strong technical capabilities, communication skills, teamwork abilities and initiative. Demonstrated ability to work effectively with vendors and resolve issues in a timely and structured manner. Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR

Our Client a global leader in advanced materials and engineered solutions. They are now seeking a Process Engineer to join their team in Limerick and contribute to driving operational excellence and innovation. Summary Under the direction of the Plant Manager, the Process Engineer will provide the Operations and Sales Teams with engineering support related to service products and process developments/qualifications. The Process Engineer will provide engineering support to drive cost/efficiency (yield and labour) improvements and cycle time reduction in our existing product and service portfolio, as well as to support new business opportunities. He/she will also assist with investigation and proposal of new equipment, procedures and methods to improve our processes. Essential Duties and Responsibilities Continuous Improvement: Troubleshoot problems with existing equipment and processes. Recommend solutions to such problems and implement solutions after review. Investigate and propose new production procedures and methods to automate, improve, and bring efficiencies to existing processes. Utilising the General Process Change control system, complete implementation of changes, providing progress reports and outcome evaluations. Runs test programs to identify key variables for process optimization using sound Continuous Improvement techniques (such as ANOVA, DOE). Collect and analyze data from tests. Develops conclusions and recommendations for process improvement(s). Assist with Ramp Plan, Control Plan and Sourcing Plan processes. Completes Continuous Improvement projects utilizing Six Sigma & Lean techniques that improve key metrics (Cost of Quality, Customer Complaint metrics, Yield, Productivity) that increase organizational effectiveness and reduces cycle time. Act as the 8D champion for complaint resolution including root cause analysis, corrective action, and preventative actions for any complaints for the assigned area. Product & Process Development: Working with Product Development and T&I to follow the New Product Development process completing the Manufacturing sections related to Process Travelers, Work Instructions, SOP, training, etc. Develops SOPs and Process Flow Diagrams for new products/services or modified equipment and procedures. Complete General Process Change control documents when implementing process changes on assigned production processes. Develop standard work and assist with training operators. Communicate and work with Sales and off-site teams where required to link in with our customers engineering teams Process Control: Complete Process Audits and resolve audit findings. Determines critical process metrics that can be monitored on a regular basis. Ensure that safety and process hazard reviews are conducted for new or modified equipment and procedures. Develops and maintains Value Stream Maps, FMEAs, Control Plans etc. for assigned processes. Apply Six Sigma principles to drive process improvements. Supervisory Requirements: Act as Project Leader for continuous improvement and corrective action teams. Act safely and ethically at all times and work in partnership with the EHS & Quality Depts. Uphold and act according to our values, mission, and vision. Assists T&I in New Process Development Stage Gate reviews. Assists in all Change Control processes. Capital Investment: Assist local leadership team in development and execution of Capital Investment Plans for the Facility; Partake in development of investment strategies aligned with corporate and local goals. Partake in individual project budgeting and planning Partake in managing individual projects through execution, ensuring on-time and within-budget delivery. Partake in establishing and maintaining relationships with vendors, contractors and other stakeholders General support for all EHS, Continuous Improvement or Growth opportunity projects. Qualifications Bachelors degree in Engineering. Prefer field of study in: Materials Engineering, Chemical Engineering, Mechanical Engineering or Manufacturing Engineering. Experience: Experience in manufacturing processes required. Direct technical experience working in the PVD industry preferred but not necessary Previous experience in the Semiconductor or Data Storage Device Industry preferred but not necessary Strong materials/metallurgy background preferred but not necessary Experience in Lean Six Sigma practices Green or Black Belt certified preferred Advanced CAD (Solid Works or AutoCAD), MS Office IT skills and Statistical Software. Excellent interpersonal, written & ICT skills Strong communication skills both with customers and internally Able to work cross functionally across technology, operations, quality Detail oriented, & self-motivated Ability to manage multiple tasks and to meet deadlines Ability to lead project groups that consist of team members with varying skills and knowledge. All applicants must be eligible to work in Ireland and hold a valid work visa as no sponsorship available for this position. Skills: Process Optimization & Continuous Improvement Process & Product Development Technical & Analytical Proficiency

Process Engineer What you need to know: An industry leader in environmental and infrastructure services is seeking a Process Engineer to join their based in Dublin 4. This full-time, on-site role offers the opportunity to join a well-established organisation delivering vital services across Ireland, with a strong focus on sustainability, operational excellence, and long-term partnerships. Your New Job: The Process Engineer will play a key role overseeing and managing processes, as well as implementing process improvements, across all stages of the wastewater treatment system. Process Engineer Responsibilities: Oversee and optimise wastewater treatment processes, including water, sludge, and thermal streams. Manage and lead a team of sampling and odour technicians. Conduct process improvement projects and analyse operational data to enhance performance. Prepare reports, present findings, and engage with stakeholders, contractors, and operations teams. What are we looking for? Postgraduate qualification (MSc or PhD) in chemical engineering, environmental or microbiological science, or a related field. Knowledge of wastewater treatment processes and process optimisation. Relevant industrial experience, preferably with process safety. Willingness to travel occasionally to other company locations in Ireland and the UK. Apply for this job now by sending in a Word version of your CV. By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are kept confidential and will not be submitted to any clients without your knowledge and consent. We Value Your Trust. Skills: Process Engineering process improvement projects enviromental water treatment

New exciting opportunity now exists on our Carlow Site for a Process Engineer to join the Process Engineering Group on site and report to the Technical Engineering Manager Our new team member will serve as technical support for new product introduction (NPI) and commercial manufacturing and will participate and/or lead cross functional or single function teams including liaising with vendors or above site groups. You will typically have prior related work experience; ideally in manufacturing, preferably GMP Setting but we will consider applicants from other working environments as long as they have technology transfer experience Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable but not a necessity for this role Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. What you will do: Bring energy, knowledge, innovation, and leadership to carry out the following: Design/Author/Review/Approve/Execute qualification/validation documentation and process development studies in line with the standard approval process Design/Author/Review/Approve/Execute Execution/development of change controls Contribution to Kaizen events as appropriate Technical input into quality notification by authoring/reviewing/approving investigations Execution of equipment/qualification validation programs; including re-qualification and re-validation Support continuous improvement through Lean Six Sigma methodologies Perform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues Serve as technical engineering representative for internal technical group discussions and represent technical Operations Carlow at global technical forums Drive compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, ensuring consideration of the impact on GMP and compliance and decisions made. Accountable for compliance via documentation completion, risk assessments, closing out corrective action, participate in audits and inspections and proactively highlighting any issues around compliance Work collaboratively to drive a safe and compliant culture in Carlow May be required to perform other duties as assigned What skills you will need: In order to excel in this role, you will more than likely have: Bachelors Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline Min 3 years experience ideally in manufacturing, preferably GMP Setting Demonstrable experience of leading technical related projects Evidence of continuous professional development is desirable Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable but not a necessity Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices Report, standards, policy writing skills required Equipment and process validation Sterile filling processes and equipment Proficiency in Microsoft Office and job-related computer applications required Excellent communication, presentation, and interpersonal skills, to interface effectively with all levels of colleagues and with external customers in a team orientated manner Hybrid role once successful completion of training, occasional shift support as required based on program needs Skills: process monitoring systems operational intelligence GMP manufacturing