46 Process Engineer jobs in Ireland

Process Engineer required by CareerWise Recruitment for our multinational manufacturing client in Kilrush, Co. Clare. Permanent position. The successful candidate will possess a high level of initiative, ability to handle multiple responsibilities, and have results driven approach to ensure successful completion of projects assigned by the Quality and Technical Manager. THE ROLE: Understand and apply principles of lean & six sigma with the ability to manage projects within a World Class Manufacturing (WCM) program. Implement suitable product and process changes to satisfy Customer Specific Requirements and that of the Quality Management System (QMS). Perform Root-Cause Analysis with process and test data to implement sustainable corrective actions. Understand risk management and the process based approach to quality and drives continuous improvements Respond to manufacturing problems in a timely manner to maintain and support production. Support and coordinate the implementation of capital investment programs. Ensure site compliance to customer requirements as well as ISO9001, Food Safety & Automotive standards. Provide technical support on processing and process capabilities to Customer Service, Sales and Quality Assurance. REQUIREMENTS: A degree in Chemical/Mechanical Engineering, Materials Science or Industrial Chemistry. High level of PC skills (MS Package, Minitab, etc.) Knowledge of pFMEA, 8D, DMAIC & Kaizen processes is desirable. Self-motivated, able to make independent decisions. Strong interpersonal and communication skills. Experience in Auditing internally and externally. Knowledge and experience with IATF core tools is an advantage. Please call James Farrar today for further information on or email: CareerWise Recruitment (In Search of Excellence) Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin. By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your consent. Skills: Process Engineer Composites

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.

SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korean company with revenues of $99 billion in 2023. Our mission is to produce and deliver life-changing therapies that improve patient outcomes and save lives. The SK pharmteco Small Molecule, Europe, facility located in Swords, Co Dublin, Ireland has led the way in the development, scale-up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we have made some of the worlds most important medicines and continue to do so. Further information on SK pharmteco can be Current Need: Cpl in partnership with the SK pharmteco Small Molecule, Europe, facility located in Swords, are looking for two Process Engineers for a 12 month contract for a new API facility which is under construction on the Swords campus. This new facility will contain large scale reactors (8000L), process tanks, filter dryer and associated services/utilities to support. These roles are to support the commissioning, qualification and start-up of this new facility. Essential Responsibilities Ownership of systems during commissioning, qualification and facility start-up Operations support for equipment and automation commissioning and qualification teams Generation and update of documentation to support Project (procedures, risk assessments, post construction equipment cleaning etc.) Engage with Operations shift team to capture their input for the safe and efficient operation of the new facility. Minimum Requirements Process Engineer should have a primary degree in Chemical Engineering, Industrial Chemistry or a related science degree with 2+ years experience. Familiarity and experience of working within the Chemical / Pharmaceutical industry and knowledge of API/small molecule manufacture. Technical writing skills and proficiency in Microsoft Word Communicates directly and works effectively as part of a team Preferred Requirements Strong equipment knowledge for small molecule manufacture Emerson DeltaV experience Commissioning and validation experience Strong verbal and written communication Thorough, diligent, good attention to detail. An Operational Excellence certification (yellow, green, black belt) would be an advantage. Skills: Chemical Engineering API Small molecule Emerson DeltaV Commissioning Validation.

POSITION SUMMARY The Process Engineer reporting to the Manufacturing Operations Manager, takes responsibility and ownership for all activities associated with their assigned Product steps. Their overarching goal is to provide Technical Support within Operations to meet agreed operational targets for safety, quality and customer delivery performance The incumbent will execute restart activities to ensure that all new APIs manufactured at the site are adequately supported in line with Zoetis Policies and Global SOP requirements. POSITION RESPONSIBILITIES 1.Ensures manufacturing operations are continually supported and maintained in compliance with all quality, safety and environmental regulations. 2. Technical transfer, Scale-up & Installation of new processes & new unit operations onto and with-in the plant. 3. Support Process & Facility start-ups, initial campaigns & process optimizations 4. Complete detailed Equipment and Process assessments. 5. Project Management of wide scope cross functional projects 6. Application of Six Sigma and Lean methodologies when undertaking projects and coaching others in use of these tools as part of their application. 7. Ensure campaign preparations for individual processes are achieved to facilitate on-time campaign start-up and adherence of agreed production rate 8. Takes ownership for assigned process steps and provide process technical support as required 9. Lead cross functional investigations within operations. Use lean six sigma tools to drive root cause analysis and CAPA completion 10. The preparation and routine review of Batch Records, Cleaning Procedures, Equipment Operating Procedures, Standard Operating Procedures, Protocols and Summary Reports. These updates include actively making changes to drive improvements, increase in RFT and decrease in deviations 11. The development and update of control system recipes 12. Participation in audits, quality monitoring inspections and self-inspections as required. 13. Participation and driving of Continuous Improvement Activities - including the continuous development and improvement of Documentation, Standards and Processes. 14. Lead cycle time reduction initiatives 15. Drive EHS activities within Operations including participation in Process HAZOP or wider safety initiatives. 16. Preparation of change control packages (incl. those for International and US Markets). 17. Liaise with site Engineering for equipment/control system modification/installation. SYSTEM OWNER / SUBSYSTEM OWNER RESPONSIBILITIES System Owner (SO) System Owners have overall accountability for the site Quality Systems for which they are responsible and in particular for: Providing strategic & proactive direction with respect to the System (across the site) in terms of content and execution. Providing support, guidance & coaching to Sub System Owners (SSO). Ensuring that SSO regularly review sub-systems for their effectiveness, escalating issues where required to site Quality Council (QRC) for action & remediation. Owning relevant System issues in the site Compliance Plan. Defining resources as needed & communicating resource needs to Site Lead. Applying people change control across Sub-Systems within their responsibility. Ensuring that SSO have proactive continuous improvement plans for their Sub-Systems. Sub System Owner (SSO) Sub-System Owners have overall accountability for the site Quality Sub-Systems for which they are responsible and in particular for: Providing strategic & proactive direction with respect to their Sub-System (across the site) in terms of content and execution. Regularly reviewing their Sub-System & presenting Sub-System review to Quality Council (QRC) as required. Escalating issues where required to the System Owner (SO) and site QRC for action and remediation. Owning relevant Sub-System issues in the site Compliance Plan. Defining resources as needed & communicating resource needs to SO. Developing & implementing proactive continuous improvement plans for their subsystem. In partnership with the SO, ensuring that there are clearly defined expert(s) for each sub-system, acting as a point of contact during inspections. Overseeing all documents associated with their sub-system and providing input to the document owners during updates. Providing comments on new/revised draft policies and guidelines and completing impact assessments where required. ORGANIZATIONAL RELATIONSHIPS Experience: ? 3 to 5 years, experience in a technical role in the API industry Education: ? Degree in Chemical/Process Engineering or Chemistry TECHNICAL SKILLS AND COMPETENCIES REQUIRED ? Strong leadership, communication, decision making and problem solving skills ? Experience with 6 sigma or other operational excellence tools ? Experience of working in a cross functional team in a highly regulated environment ? Experience of technology transfer and a new product/equipment start-up ? An understanding of computer control systems, P.I.D loops and interlock devices ? Ability to manage multiple projects simultaneously and prioritise work, goals and tasks in accordance with division and corporate objectives PHYSICAL POSITION REQUIREMENTS ? This is Rathdrum site based position. ? This position will require fluent use of teleconferencing and WebEx tools, as well as SharePoint technologies, to share and manage information with Global GMS and other Zoetis internal API manufacturing network Full time Legal statement as below This job advert indicates the general nature and level of work expected. It is not designed to cover or contain a comprehensive listing of activities or responsibilities required of the incumbent. Incumbent may be asked to perform other duties as required. Additional position specific requirements/responsibilities are contained in approved training curricula. Visa status re must be eligible to work and live in Ireland as below Colleague must be legally eligible to live and work in Ireland. Summary of our Benefits In addition, to being part the world leading animal health company focused on the needs of those who raise and care for animals we offer a range of benefits such as competitive salary, bonus, 25.5 days holiday per annum plus public holidays, a defined contributory pension plan, private medical insurance for you and your family and empowered flexible working, to name a few. Please note that the benefits outlined are subject to change based on organization decision. 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 Apply button below to Login/Register.

A Process Engineer is required by CareerWise Recruitment for our Waterford based Pharmaceutical Client. This is a 12-month contractor position. If you are interested in working in a Sterile environment working and supporting technical transfers then this is the position for you ! THE ROLE: Deliver projects works under the bracket of continuous improvement in the existing thawing, formulation, filling, filter integrity testing and wash/autoclave areas to support NPI and capacity expansion including but not limited to single use technology vendor selection, component introduction and qualification. 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. Provide support on the existing Aseptic Syringe Filling Lines which includes Debagger / Ebeam / Delid / Deline / Isolator / Syringe filling machine with multi filling technologies. Support commercial manufacturing through delivery of key performance metrics (SQDCI). Support and participation in Regulatory Audits REQUIREMENTS: Degree in an Engineering discipline. Strong problem-solving skills. Strong documentation/protocol generation and execution skills. 3 -5 years relevant experience in a highly regulated GMP environment Experience in syringe filling would be a distinct advantage. Ability to lead major investigations Fill Weight Cycle Development experience for a filling machine New product introduction experience to a sterile manufacturing Please call Louise Mulligan today for further information on or email: CareerWise Recruitment (In Search of Excellence) Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin. By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your Skills: Process Engineer Debagger ,Ebeam ,Delid Ebeam

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the worldfrom the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries , extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. This position is based in Waterford. Duties and Responsibilities Subject Matter Expert for high volume, automated, contact lens manufacturing equipment. Support day to day operations through diagnosis and correction of line detractors. Use a data-based approach to identify the top line detractors and drive continuous improvement of existing equipment through uptime, yield and cycle time improvement projects. Organise, control and improve planned maintenance and calibration activities. Critically assess machinery to identify and source appropriate spare parts. Support site strategy and capacity expansion projects. Provide technical training to operations and maintenance personnel on an as-needed basis. Role model good safety and quality behaviours. Own, track and report on safety, quality and operational open items. Develop relevant work instructions and standard operating procedures. Writing and execute process and equipment engineering studies and protocols. Requirements Bachelor of Engineering (or equivalent) with 5+ years of experience. Master of Engineering (or equivalent) with 3+ years of experience. Demonstrated ability to optimise highly automated production lines within a regulated environment. Lean/Six Sigma and/or project management certification is preferred.

Process Engineer - Manufacturing | Limerick My client, a global leader in advanced materials, is currently seeking a Process Engineer to join their growing team in Limerick. This is a fantastic opportunity for a highly motivated and hands-on engineer who enjoys being out on the floor, driving improvements and making a real impact in a fast-paced production environment. Reporting to the Plant Manager, you will play a key role in supporting both operations and sales with process optimisation, cost reduction, and new product development. This role will suit someone who thrives in a collaborative setting, enjoys problem-solving, and wants to take ownership of continuous improvement initiatives. What you'll be doing: Taking a hands-on approach on the production floor, working closely with operators to spot and drive process improvements Troubleshooting issues and proposing solutions to enhance yield, efficiency, and cycle times Leading and supporting continuous improvement projects using Lean and Six Sigma methodologies Contributing to the development of new products, processes, and production procedures Collaborating with Sales and Product Development teams, including direct contact with customer engineering teams Supporting capital investment projects and introducing new equipment and processes What we're looking for: A degree in Engineering - ideally Mechanical, Materials, Chemical or Manufacturing Previous manufacturing experience (semiconductor, PVD or data storage a plus, but not essential) Strong problem-solving and analytical skills; familiarity with Lean Six Sigma is advantageous A proactive and hands-on approach with strong communication and teamwork abilities Confidence working with cross-functional teams and managing multiple projects This role offers the chance to work in a collaborative environment where innovation and continuous improvement are part of the culture. You'll have the opportunity to take the lead on key initiatives and contribute to the ongoing success of a highly regarded manufacturing site. To apply or learn more, please contact Kerry on or send your CV in confidence. Skills: Process Improvements Optimisation Production Benefits: Negotiable Healthcare Bonus Pension

**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
**Abbott Diabetes Care Kilkenny**
Abbott Diabetes Care has opened a new site, in Kilkenny, that is at the forefront of Diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems.
**Main purpose of the role**
Your role as Process Engineer Lead will be to provide the link between the TPM (Third Party Manufacturing) and the ADC internal organisation. You will be responsible for leading the implementation of Process, Equipment and Material Change projects, developing a close understanding of the manufacturing process and interpreting the factors that affect product performance. In addition, the incumbent will provide engineering investigation capabilities for exceptional events and implement change in an environment of continuous improvement, ensuring the site delivers safe and effective biosensor products that meet customer needs whilst maintaining compliance.
It will be a very big plus if you can bring experience in developing projects or sites from square one.
**Main responsibilities**
- As the Specialist in the Pharmaceutical/Biological Process Sub-Function, considered as highly experienced and knowledgeable resource within the organization in implementing and maintaining pharmaceutical/biological processes.
- Calculates and organizes all data for complex process flow sheets including instrumentation and control considerations.
- Models processes and units operations.
- Ensures proper sequence of operation and prepares specifications and operating instructions for processing equipment.
- Conducts tests and measurements throughout stages of production to determine control over such variables as temperature, density, pressure and viscosity.
- Services, troubleshoots, and solves engineering problems with processes or equipment already in operation.
- Ensures processes and procedures are in compliance with regulations.
- May be responsible for corrective and preventive actions and investigation management.
**Qualifications & Experience**
+ Relevant third level qualification. Engineering/Manufacturing/Science is preferred.
+ Minimum 3 years relevant work experience in a manufacturing /industrial environment.
+ Excellent communication / interpersonal skills.
+ Enthusiastic and energetic with the ability to lead a team.
+ Demonstrated flexible and innovative approach to work.
Connect with us at on LinkedIn at , on Facebook at and on Twitter @AbbottNews.
**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

**Position Summary**
+ Executes the innovation and development of assigned project elements with an emphasis on the manufacturing process, technology and procedures required for the manufacture of new products.
+ Uses latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs.
**Key Areas of Responsibility**
+ Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.
+ Ensure quality of process and product as defined in the appropriate operation and material specifications.
+ Will assist in the selection of components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols.
+ Support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
+ Will analyse equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings.
+ Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
+ Complete capability studies for in process inspection and generate subsequent Inspection documentation.
+ Conduct MSA studies for new products and new processes.
+ Provide training for manufacturing team members.
+ Ensure adherence to GMP and safety procedures.
+ Review and approval of validation documentation.
+ All other duties as assigned.
**Qualifications Knowledge Skills**
+ B.S in Mechanical Engineering or related engineering discipline with 2 or more years' experience
+ Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
+ The individual should enjoy working in a fast paced, dynamic and results orientated team environment.
+ Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams.
+ Innovative thinker - should be able to envisage new and better ways of doing things.
+ Excellent analytical skills, ability to plan, organise and implement concurrent tasks.
+ Good knowledge of manufacturing processes, materials, product and process design.
+ Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
+ Experience in an FDA regulated or regulated industry beneficial.
+ High level of PC Skills required.
+ Excellent attention to detail.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.