303 Textile Engineering jobs in Ireland

An experienced Manufacturing Process Engineer is required by Careerwise recruitment to work with our Galway based Electronics Manufacturing client.

THE ROLE:

* Work with customers on NPI projects to improve manufacturability and complete NPI projects to schedule.

* Incorporate Continuous Improvement activity based on business objectives and current cost reduction goals.

* Prepare assembly documentation and work instructions.

* Train Operatives in assembly procedures.

* Support the Maintenance Team in designing planned maintenance routines necessary for all of the SMT equipment, and, as required, perform critical Engineering Maintenance tasks.

* Provide technical support to production.

* Implement process controls such as FMEA and Control plan as part of the Change Management process.

REQUIREMENTS:

* L8 qualification in a manufacturing related engineering discipline or equivalent.

* Experience working with engineering bill of materials and drawings.

* Flexibility to undertake overtime or working on the weekends according to business needs.

* Demonstrable working knowledge of SMT components and processes.

**Join SPX FLOW as Process Engineer

Dunboyne – Ireland**

About The Role
We are currently seeking a talented and motivated
Process Engineer
to join our team. In this role, you will be involved in both project execution and bid proposal development, taking responsibility for the process design of equipment systems and components. You will contribute to the delivery of high-quality, cost-effective process solutions in line with project timelines and customer requirements.

This is an exciting opportunity to be part of a collaborative, multidisciplinary engineering team, where your technical expertise will directly influence the success of our projects across industries such as Dairy, Food, Beverage, and Pharmaceutical.

Key Responsibilities
As a Process Engineer, your main duties will include:

• Process Design:

• Developing process flowsheets, P&IDs, equipment specifications, and operating instructions.

• Performing process calculations (e.g. pipe sizing, pump selection, thermal balances).

• Defining input/output requirements, utilities, KPIs, and performance metrics.

• Safety & Compliance:

• Ensuring plant designs are safe and environmentally responsible.

• Adhering to applicable legislation (e.g. EU Machinery and PED Directives).

• Participating in design and risk reviews.

• Project Delivery:

• Ensuring timely delivery of design outputs to the required quality and within budget.

• Supporting & leading installation and commissioning teams to ensure design intent is met.

• Assisting with documentation handover and support to Aftermarket teams.

• Collaboration & Communication:

• Working closely with internal teams including Mechanical, Electrical, and Automation.

• Participating in project meetings, design reviews, and technical discussions.

• Providing input to sales teams, feasibility studies, and customer site surveys.

• Documentation:

• Preparing operating manuals and spares lists.

• Supporting technical file compilation in line with relevant regulations.

• Leadership (when applicable):

• Acting as Lead Engineer on selected projects, coordinating multidisciplinary teams.

• Managing schedules, resources, and ensuring consistent design standards.

• Engineering Community Engagement:

• Acting as a subject matter expert and mentor where appropriate.

• Supporting continuous improvement initiatives and knowledge-sharing activities.

Qualifications & Experience

• Degree in Process, Chemical, Mechanical Engineering, or a related discipline
• Engineering design experience in hygienic industries (e.g. Dairy, Food, Beverage, Pharma)
• Understanding of hygienic and CIP (clean-in-place) design principles
• Proficiency in Microsoft Office; AutoCAD and SAP experience a plus
• Full driving license
• Fluent in English (spoken and written)
• Strong communication and interpersonal skills
• Ability to manage multiple tasks and work within a matrix structure
• Self-motivated with strong analytical and problem-solving skills
• High ethical standards and a collaborative mindset

What We Offer

• Competitive salary package with annual performance-based bonuses.
• Recognition and performance incentive programs.
• Opportunities for professional growth within a global, innovative company.
• A supportive work environment committed to sustainability and technological advancement.

Next Steps
Does this opportunity align with your career goals? If you're ready to contribute to innovative solutions with a global impact, we would love to hear from you.

Apply now to join a team that is shaping the future of process systems.

For any questions, please feel free to reach out to the recruiter, Olena Kril at

About SPX FLOW
At SPX FLOW, Inc., we specialize in creating innovative flow components and systems. With over 100 years of experience, we offer 20 brands of pumps, valves, mixers, air dryers, hydraulic tools, homogenizers, separators, heat exchangers, filtration solutions, and more. Our products help produce many of your favorite household goods and snacks

Headquartered in North Carolina, we operate in over 25 countries with 5,000 employees worldwide. We are committed to sustainability, holding over 550 patents globally, with 44% focused on clean technology. Join us and be part of a company that values innovation and sustainability.

FULL TIME

Cork, Ireland

Process Engineer (Validation Engineer)

Réalta Technologies are looking for a Process Engineer (Validation Engineer), this role sits within a specialist engineering team supporting the development and manufacture of innovative medical device solutions.

The Process Engineer will provide technical and validation support across manufacturing and project activities, driving process improvements, ensuring compliance, and supporting the introduction of new products and technologies.

Key Responsibilities

• Lead and support process validation activities (IQ, OQ, PQ) and maintain compliant documentation
• Provide engineering input for new product and process introductions
• Drive continuous improvement initiatives to enhance quality, cost, and efficiency
• Support troubleshooting, root cause analysis, and implementation of corrective actions
• Develop and maintain SOPs, work instructions, and other GMP documentation
• Collaborate with cross-functional teams and external partners to deliver on project goals
• Ensure all work complies with Quality and EHS requirements.

Qualifications & Skills

• Level 7/8 Degree in Mechanical, Process, or related Engineering discipline.
• 2–4 years' experience in a regulated manufacturing or medical device environment.
• Strong understanding of process validation and Six Sigma or problem-solving tools.
• Proven project management and analytical skills.
• Excellent communication and collaboration skills.
• Self-motivated, adaptable, and technically curious.

Job Duties Outline job duties/responsibilities below:

• To ensure that engineering, qualification & validation records are developed and maintained as per the cGMP and GDP requirements & SOP.
• Coordination with design consultant as required and respective user department for the design of process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.).
• Review & approval on detailed design as submitted by vendors (e.g. Manufacturing Vessel, Blender, Filling lines etc.).
• To ensure project execution work and follow-ups with different departments (QA, QM, Operations etc.) to meet the project completion within stipulated time frame.
• Effectively communicate & discuss related to day to day activity and concerns within team for efficiency and performance improvement.
• To prepare, review & update of standard operating procedures at regular intervals to meet cGMP requirements.
• To ensure the compliance of current Good Manufacturing Practices of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.).
• To ensure that Preventive Maintenance is developed for relevant equipment/processes in co-ordination with the relevant departments as per schedule.
• Responsible for development, execution and review of Qualification / Re-Qualification and Validation activity of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.)
• To ensure the compliance of Engineering Department activities as per Quality management system.
• Review & verification of Engineering department standard operating procedures at regular intervals to meet cGMP & Regulatory requirements.
• To carry out FAT/SAT activities as required for newly installed equipment/Systems.
• Installation and Operational qualification activity of related process/manufacturing equipment (Manufacturing Vessel, Blender, Filling lines etc.).
• To ensure the calibration of relevant Engineering Department instruments are performed as per validation requirements and documented as required per cGMP requirements.
• To ensure that all Engineering changes are assessed and implemented as per cGMP and local SOP.

Elusav Recruitment have an excellent opportunity for a Process Engineer to join a leading Global Biopharma company in Waterford.

Reporting to the Team Lead, the Process Engineer will play an integral role within the Product Supply Unit's team, ensuring reliable supply of syringe and vial products to our patients globally.

Responsibilities:

• Provide process engineering support to the Product Supply 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 with a distinct focus on AVI inspection.
• 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.
• Support all company safety and quality programs and initiatives.

Requirements:

• Experience in a highly regulated GMP environment.
• Degree in an Engineering discipline.
• Strong documentation/protocol generation and execution skills.
• Automation experience with vision systems is desirable.

Contact:

If you would like to learn more about the vacancy, apply now, or contact Stephen O'Brien on or

Global Biotechnology company, based in south Dublin, Ireland - looking for
Process Engineer Scientist.
The candidate will be responsible for supporting small and large molecule drug product manufacturing at company facilities. As part of our global Process Development organization, they will be key in ensuring the highest standards of process performance, while providing process and product support to inspected drug product operations.

The Job:

• Independently perform design and qualification activities.
• Author and / or reviewer of protocols, reports and technical assessments.
• Supports make-a-batch exercises to determine facility fit and identify gaps in the Visual Inspection process.
• Supports New Product Introduction with visual inspection method development and AVI characterization for new inspection lines.
• Provides expertise on defects identified during batch inspection and supports defect library updates.
• Supports in the development of visual inspection team members by allowing new members to shadow them.
• Support in the characterisation and qualification of AVI vision recipes as part of process improvements.
• Provides support for manufacturing and commercial activities.

Have You:

• Bachelor's degree in Science, Engineering or relevant discipline with 2- 3 year's experience in a similar role OR Master's degree & 2 years of directly related experience.
• Experience in a regulated and or vision related work environment
• 3+ years of drug product process development experience in the pharmaceuticals/biotechnology industry.
• Knowledge of/hands-on experience with end-to-end development for liquid and lyophilized drug products in various presentations.
• Should be interested in working in a team of like-minded inquisitive people who serve the operations team by providing solutions to their inspection needs.
• Independent thinker with demonstrated skills working in teams.
• Strong Interpersonal and communication skills.

The successful candidate must have eligible working VISA in Ireland or European Union (EU) passport.

Berkley Life Science & Engineering is a specialist consultancy, recruiting professionals for organizations throughout Ireland, UK & Europe; for more information go to

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone Aleksas Kremenskas at or send your profile to -

Purpose
New exciting opportunity now exists 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.

Responsibilities

• 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 requalification 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
• May be required to perform other duties as assigned

Qualifications

• 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
• 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 O

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.

Ascend PM are hiring a Process Engineer Scientist to join our clients team, a multinational biopharmaceutical company based in Dublin. This is a great Contract opportunity to join a growing team. Initially 12 Month Contract with view to extend. Contact or email CV to to find out more.

Overview:

The successful candidate will be responsible for supporting small and large molecule drug product manufacturing. As part of our global Process Development organization they will be key in ensuring the highest standards of process performance, while providing process and product support to inspected drug product operations.

Key Responsibilities:

• Independently perform design and qualification activities.
• Author and / or reviewer of protocols, reports and technical assessments.
• Supports make-a-batch exercises to determine facility fit and identify gaps in the Visual Inspection process.
• Supports New Product Introduction with visual inspection method development and AVI characterization for new inspection lines.
• Provides expertise on defects identified during batch inspection and supports defect library updates.
• Supports in the development of visual inspection team members by allowing new members to shadow them.
• Support in the characterisation and qualification of AVI vision recipes as part of process improvements.
• Provides support for manufacturing and commercial activities.
• Leads or assists in process related deviations, exception resolution and root cause analysis to ensure smooth operations & continued supply. Assists in troubleshooting issues with drug product processing technologies and equipment.
• Is Audit ready to support during GMP Audits.

Experience & Qualifications:

• Bachelors degree in Science, Engineering or relevant discipline with 2- 3 years experience in a similar role
• Experience in a regulated and or vision related work environment
• 3+ years of drug product process development experience in the pharmaceuticals/biotechnology industry
• Knowledge of/hands-on experience with end-to-end development for liquid and lyophilized drug products in various presentations
• Should be interested in working in a team of like-minded inquisitive people who serve the operations team by providing solutions to their inspection needs