213 Equipment Engineer jobs in Ireland

PSC Biotech is seeking a
Bioprocess Engineer
to join our client's in Limerick. This role provides both
technical process design support
for bio process systems on new CAPEX projects and
ongoing operational support
for commercial manufacturing processes.

Key Responsibilities

CAPEX / Project Support

• Generate User Requirement Specifications (URS) for assigned systems.
• Review and approve Basis of Design (BOD) and detailed design deliverables (e.g., PFDs, P&IDs).
• Ensure procurement packages (BOMs, datasheets, cutsheets, etc.) meet equipment specifications.
• Track and resolve HAZOP action items, ensuring integration into system design.
• Participate in 30%, 60%, and 90% design model reviews to confirm compliance with operational, safety, and ergonomic standards.
• Review and approve system lifecycle documentation (FS, SDS, IO lists, etc.).
• Support FAT/SAT and commissioning activities, including development of protocols.
• Ensure Vendor Document Requirements (VDR) meet client standards.
• Build Preventative Maintenance (PM) tasks and spare parts lists on CMMS.

Operational / Manufacturing Support

• Act as a technical SME for assigned bioprocess equipment and systems.
• Support manufacturing operations through troubleshooting, deviation resolution, and root cause analysis.
• Monitor process performance, analyze data trends, and recommend improvements.
• Provide technical input to change controls, CAPAs, and risk assessments.
• Support technology transfer activities, ensuring successful scale-up and integration of new processes into manufacturing.
• Collaborate with Manufacturing, QA, and Process Sciences to ensure robust and compliant operations.
• Drive continuous improvement initiatives to enhance reliability, yield, and efficiency.

Requirements

Requirements

• Bachelor's degree in chemical, Process, or Mechanical Engineering (or equivalent).
• 3–5 years of relevant engineering experience; direct experience with biopharmaceutical process equipment preferred.
• Background in process design, commissioning, and/or manufacturing support within the biopharmaceutical sector is highly desirable.
• Strong problem-solving and data analysis skills with the ability to support root cause investigations.
• Familiarity with automation platforms such as DeltaV is an advantage.
• Equivalent experience may be considered in place of formal education.

We are seeking an experienced Senior Equipment Engineer to support a major manufacturing expansion for our pharmaceutical client in Dublin. This role will focus on the engineering implementation and operational setup of new syringe filling, inspection, washing, and formulation systems within a sterile fill-finish environment.

Key Responsibilities

• Support all engineering and equipment activities for the installation and startup of syringe filling, inspection, washing, and formulation systems.
• Lead and participate in FAT, SAT, commissioning, and qualification phases to ensure equipment readiness for GMP manufacturing.
• Coordinate equipment setup, calibration, and functional testing, ensuring alignment with site engineering and quality standards.
• Collaborate closely with Manufacturing, Quality, Automation, PD, and Global Engineering to ensure seamless integration of new systems.
• Support change control, validation, and documentation activities in compliance with cGMP and site procedures.
• Contribute to the development of preventive maintenance and calibration programs for new equipment.
• Provide technical troubleshooting during installation and startup, ensuring timely resolution of engineering issues.
• Prepare and review engineering deliverables including specifications, FAT/SAT protocols, and handover packages.
• Work flexibly, including extended days or two-cycle shift coverage during critical commissioning and qualification phases.

Qualifications & Experience

• Bachelor's Degree (or higher) in Mechanical, Electrical, Chemical, or related Engineering discipline.
• 4+ years' experience in a GMP manufacturing or project engineering role within the biopharmaceutical or sterile fill-finish sector.
• Demonstrated experience with syringe filling, inspection, or formulation systems.
• Proven capability in equipment commissioning, qualification, and validation.
• Strong knowledge of GMP, regulatory, and quality systems.
• Hands-on experience managing FATs, SATs, and vendor interactions.
• Excellent communication, teamwork, and problem-solving skills.
• Self-starter with the ability to work in a small project team and adapt to evolving priorities.
• Flexibility to support on-site and extended-hour work during key project milestones.

Biologics Process Equipment Engineer

We are seeking a highly motivated
Process Equipment Engineer
to join our clients
Biologics Operations
team. This role supports the design, commissioning, validation, and lifecycle management of manufacturing equipment, ensuring alignment with safety, quality, and regulatory standards. The successful candidate will act as the equipment SME from the design phase through to handover, supporting both ongoing operations and new product introductions.

KEY RESPONSIBILITIES

PROJECT & PROCESS ENGINEERING:

• Act as SME for vial filling and isolator systems from design to validation.
• Review and approve PFDs, P&IDs, layouts, and specifications.
• Lead FAT/SAT activities and oversee vendor interactions to ensure compliance with site and regulatory requirements.
• Support equipment integration, installation, commissioning, and validation.

OPERATIONAL SUPPORT:

• Develop and update procedures to align with manufacturing and regulatory needs.
• Troubleshoot equipment issues, investigate process deviations, and coordinate technical resolutions.
• Ensure ongoing equipment performance, process optimization, and adherence to maintenance strategies.

VALIDATION & COMPLIANCE:

• Develop commissioning and validation strategies following Good Engineering Practice (GEP).
• Review and execute validation protocols ensuring alignment with project timelines.
• Ensure readiness for audits and inspections by upholding cGMP, ISO, and FDA standards.

COLLABORATION & LEADERSHIP:

• Work closely with cross-functional teams (Operations, Quality, S&T) to support equipment lifecycle.
• Mentor and provide guidance to peers and contractors; lead training where applicable.
• Drive continuous improvement and support cost-saving initiatives and new technology integration.

QUALIFICATIONS

• Bachelor's or Master's degree in Engineering, Science, or a related technical discipline.
• Minimum 5 years of experience in equipment or process engineering within the pharmaceutical or biotech sector.
• At least 3 years' experience in GMP manufacturing environments.
• Knowledge of parenteral drug manufacturing, sterilisation, and aseptic processing is highly desirable.
• Experience with new product introduction and tech transfer is advantageous.

SKILLS AND COMPETENCIES

• Strong problem-solving ability under pressure.
• Detail-oriented with a focus on compliance and operational excellence.
• Excellent verbal and written communication skills.
• Strong interpersonal and stakeholder management capabilities.
• Ability to work independently and make informed technical decisions.
• High level of integrity and commitment to quality.
• Familiarity with automation/control systems and their impact on processes.

ADDITIONAL EXPECTATIONS

• Support EHS policies, actively report incidents or unsafe conditions, and contribute to a safe working environment.
• Wear appropriate PPE and attend all required safety and compliance training.
• May supervise contractors or lead cross-functional project teams.
• Will have external contact with vendors, engineers, and auditors.

Senior Equipment Engineer

The Senior Equipment Engineer will be responsible for the ownership, qualification, process ownership, and continuous improvement of advanced automated manufacturing equipment. This includes systems that integrate robotics, machine vision, servo motion control, pneumatics, and PLC-based automation. The role requires a hands-on engineer with strong technical expertise to ensure high equipment uptime, process stability, and regulatory compliance.

Key Responsibilities:

• Serve as the primary owner for automated manufacturing equipment, covering mechanical, electrical, pneumatic, and control subsystems.
• Develop and execute equipment qualification protocols (IQ, OQ, PQ) to support regulated manufacturing operations.
• Troubleshoot and resolve equipment issues involving PLCs, servo drives, robotics, HMIs, machine vision systems, and pneumatic circuits.
• Drive preventive and predictive maintenance programs to maximize uptime and equipment reliability.
• Support new product introductions by adapting equipment tooling, automation sequences, and test protocols.
• Collaborate with cross-functional teams to improve throughput, yield, and OEE through equipment enhancements.
• Partner with equipment vendors on upgrades, retrofits, spare parts management, and FAT/SAT processes.
• Provide training and mentorship to technicians and junior engineers on equipment operation and troubleshooting.
• Ensure compliance with EHS standards and lockout/tagout requirements during interventions.

Required Qualifications:

• Bachelor's or Master's degree in Manufacturing Engineering, Mechanical Engineering, Electrical Engineering, Mechatronics, or related field.
• 7+ years of experience in equipment or automation engineering in a regulated manufacturing environment (medical device, pharma, or similar).
• Demonstrated expertise in:
• PLC programming and troubleshooting (Allen-Bradley, Siemens, or equivalent).
• Robotics integration for assembly and material handling.
• Machine vision systems (Cognex, Keyence, or similar).
• Servo and motion control systems.
• Pneumatic control and automation.
• Strong background in equipment validation and regulatory compliance.
• Excellent problem-solving, project management, and cross-functional communication skills.

Preferred Qualifications:

• Experience with high-speed automated assembly and inspection equipment.
• Lean Six Sigma Green or Black Belt certification.
• Knowledge of GMP requirements and cleanroom automation.
• Proven ability to manage vendors and negotiate technical requirements.

Job Description
We are excited to announce a fantastic opportunity for a Senior Equipment Engineer at our state-of-the-art site in Dundalk. Our facility is dedicated to formulating and filling vaccine products that improve and transform lives globally.

This role offers a unique opportunity to provide technical leadership and support for Vial Filling Equipment and associated machinery. By joining our team, you will play a crucial role in improving and transforming lives globally.

Your Core Responsibilities

• Provide technical leadership within a new Vaccine DP facility, ensuring equipment safety, effectiveness, and compliance.
• Adhere to company and site engineering policies and procedures, and review/authorship of testing protocols, reports, and manufacturing SOPs.
• Lead Commissioning & Qualification activities for new equipment and manage Equipment Vendors, including SAT, maintenance visits, and continuous improvement projects.
• Participate in cross-functional teams to troubleshoot technical issues, drive continuous improvement, and process optimization using DMAIC and FMEA tools.
• Manage changes to equipment/process as per site change control procedures and support the establishment of a Preventative Maintenance Program.
• You will have the opportunity to lead/participate in equipment-related manufacturing investigations to ensure root cause analysis, impact analysis, and CAPAs implementation.
• Provide technical expertise during regulatory inspections and support the transition from project to sustaining manufacturing, improving equipment reliability.
• Collaborate with the IPT Leader and multiple partners to ensure effective strategies, direction, and excellence in IPT/maintenance programs.
• Provide technical expertise during regulatory inspections e.g. FDA, HPRA inspections to defend systems, change controls, investigations and qualification packages

Who You Are
You are ready if you have

• Technical expertise in machine and equipment maintenance programs within a regulated cGMP environment.
• Proven ability to lead Commissioning & Qualification activities and manage Equipment Vendors and continuous improvement projects.
• Strong understanding of cGMP activities including RA and CQV protocols/reports.
• Ability to troubleshoot and resolve technical issues using DMAIC and FMEA tools.
• Experience in managing changes to equipment/process as per site change control procedures and leading/participating in equipment-related manufacturing investigations.
• Experience in regulatory inspections (e.g., FDA, HPRA inspections).

Nice to have, but not essential

• Experience in the pharmaceutical or biopharmaceutical industry.
• Knowledge of Preventative Maintenance Programs for equipment in Drug Product suites.
• Lean or Six Sigma experience.

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description
As a company, we are committed to keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to
Invent solutions to meet unmet healthcare needs,
please apply today.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status
Regular

Relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Not Applicable

Shift
Valid Driving License
Hazardous Material(s)
Required Skills
Adaptability, Analytical Problem Solving, cGMP Regulations, Change Control Procedures, Commissioning, Decision Making, FDA Regulations, Manufacturing, Manufacturing Operations, Preventive Maintenance, Process Improvements, Safety Standards

Preferred Skills
Lean Six Sigma (LSS), Pharmaceutical Product Development

Job Posting End Date
09/20/2025

• A job posting is effective until PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID
R

Emerald Catering Equipment Ltd is a leading independent specialist in commercial catering equipment. We provide a full range of services to businesses across the Leinster area. Our clients range from small independent restaurants to large corporate canteens, hospitality venues, and industrial facilities. We pride ourselves on our hands-on expertise, customer-first approach, and commitment to providing reliable, energy-efficient solutions.

We are seeking a skilled Commercial Catering Engineer to join our team. In this role, you will install, service, and maintain a wide range of commercial catering equipment, ensuring it operates safely and efficiently. You will troubleshoot technical issues, deliver effective solutions, and provide high-quality service while maintaining professional communication with clients.

Key Responsibilities:

• Install, commission, and maintain commercial catering equipment, including ovens, fryers, grills, dishwashers, and other kitchen appliances.
• Undertake maintenance, servicing, installation and repair work according to client specifications.
• Diagnose electrical and mechanical faults with a focus on first-time resolution.
• Produce accurate service reports, installation documentation, and client paperwork.
• Participate in on-call, and standby, at weekends only.
• Deliver exceptional customer service professionally and courteously.
• Adhere strictly to health, safety, and environmental regulations on site.
• Maintain company-issued tools and equipment in a clean, safe, and serviceable condition.
• Ensure all documentation is completed accurately in line with statutory compliance.
• Communicate the status of work to the Helpdesk and assist in promoting operational efficiency.
• Attend review meetings and build strong working relationships with clients and colleagues.

Benefits:

• On-call system. There is no mandatory on-call rotation. However, optional overtime is available.
• 21 days of annual leave.
• Company Van and Fuel Card.
• Mobile Phone.

Qualification & Experience:

• Minimum of 7 years' experience in commercial catering equipment industry.
• Full clean driving license.
• Fluency in English is must.
• Prior experience with commercial refrigeration is a significant advantage, but not essential. We will provide training for the right candidate.

Job Types: Full-time, Permanent

Pay: €45,000.00-€65,000.00 per year

Benefits:

• Company car
• Wellness program

Work Location: On the road

The Project / Equipment Engineer reports to the Senior Manager for Strategic Engineering Projects and is responsible for scoping and executing technical projects supporting Drug Product manufacturing within Formulation, Component Preparation, Vial/Syringe Filling, Lyophilisation, Device Assembly, Inspection, Filter/Filter Integrity Testing areas. This includes qualification of new equipment and implementation of associated reliability and maintenance programs.

Key Responsibilities:

• Project management and execution of assigned projects including project prioritization, resources management, status management and external communication.

• Working with various stakeholders, to scope projects and ensure requirements are satisfied. Project input will span from concept, through design, construction, commissioning and operation

• Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification & start-up

• Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.

• Ability to translate strategic/emerging technology solutions into pragmatic executable plans

• Development and management of change controls

• Participate as a member of multidisciplinary site and multisite teams

• Development of detailed specifications, engineering documents, protocols and standard operating procedures

• Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations.

• Works in a collaborative manner with the System Owners, Maintenance Supervisors & Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.

• Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures

• Support a safe working environment by complying with environmental health/safety practice, rules and regulations

• Travel may be required to support execution of projects

Experience and Qualification:

• Bachelor's Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience

• Typically, 3+ years engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment or Automated Inspection and/or Automated Device Assembly,

• Proven project management experience.

• Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous

• Demonstrated experience in a GDP Compliant environment.

• Experience in MS Office, MS Project, Change Control & Document Management Systems

• Proven ability working cross functionally, delivering technical solutions and implementing improvements.

• Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results

• Technical report writing and communication/presentation skills

• Data driven decision maker

• Ability to work to tight deadlines in a fast-moving environment

Sustainability that means business
Who We Are
Sustainability software specialist, AMCS, is headquartered in Ireland, with offices in Europe, USA, Canada and Australasia. With over 1,300 highly-skilled employees across 22 countries, we specialize in delivering technology solutions to facilitate a carbon neutral future.

What We Do
Our innovative SaaS solutions increase efficiency and boost sustainability in resource-intensive industries. Over 5,000 customers across 23 countries already benefit from our Performance Sustainability software, ensuring we deliver practical solutions for improved profitability and environmental resilience across the globe.

Our people
AMCS offers team members more than just a job, but an opportunity to map out a career with a company that is growing, evolving and setting out new ways of working that are having a positive impact on the world around us. AMCS was established in Ireland and holds onto those local roots and 'start-up' mentality with a culture of connection. Connection to our work, our customers, our colleagues and our community that creates a working environment that fosters openness, collaboration and creativity.

The Customer Process Improvement Specialist is responsible for analysing, developing, and implementing strategies to enhance operational efficiency, reduce costs, and improve overall business processes. Initiate & oversee Customer Support Continuous Improvement projects, including defining scope, timelines, and delivery. They will work closely with stakeholders to identify inefficiencies, implement best practices, and drive continuous improvement initiatives across the organization.

Job Specification-Roles & Responsibilities

• Drive continual improvement that guides AMCS to improving the customer experience.
• Investigating, analysing, and documenting the current state of business processes.
• Leveraging Lean Six Sigma tools and methodology as applicable.
• Drive improvements to existing processes and identifying areas of non-value waste.
• Owner of Global process standardisation and optimisation.
• Identify problem customer trends and initiate remediation plans.
• Initiate & oversee Continuous Improvement projects, including defining scope, timelines, and delivery.
• Once process improvements have been identified ensure they are rolled out globally and followed consistently.
• Improvement focus will include streamlining our ServiceDesk system of record, to provide insights into improving processes, usage & training.

Candidate Profile

• Degree in Business Administration, Operations Management, Industrial Engineering, or a related field.
• Certifications in Lean, Six Sigma (Green Belt or higher), or other process improvement methodologies are a plus.
• Proactive, positive, self-starter with a passion for continually improving the processes around you.
• Ability to work independently as well as within a team environment.
• Excellent oral and written communication skills with both technical and non-technical audiences.
• Possess interpersonal skills, successful at developing and managing relationships at all organisational levels, both internally and externally.
• Proven track record of successfully leading process improvement initiatives.
• Experience in the SaaS Operations an advantage.

Overview:

Job Description – Process Improvement Specialist

Short Overview of Job Responsibilities

This role is a key position within a newly created team responsible for the delivery of process

innovation and continuous improvement initiatives across multi-jurisdictions. It will play an important role in helping to foster a culture of sustainable change through the creation and embedding of

Teleperformance methodology and the supporting framework to deliver business transformation.

Responsibilities:

• To identify and deliver service improvement activity across the business through employing

process improvement methodologies and the application of innovative thinking

• To work with key business stakeholders to build a continuous improvement environment to

support an ongoing programme of change

• To support the delivery of better value and greater efficiency through the identification and

elimination of unnecessary complexity within business processes and identification of better

ways of working

• To identify trends and process variations as part of establishing a continuous improvement

monitoring system

• To assist in the development and implementation of a 'best-in-class' continuous improvement

strategy

• To take ownership of change initiatives from evolution/efficiency identification through to

project delivery via internal governance and controls

• To elicit requirements and drive process change using staff interviews, document analysis,

requirements workshops, surveys, site visits, business process descriptions, business analysis

and workflow analysis

• To work with other team members and business services departments to devise new support

material based on the revised processes, to include training, reporting and systems

enhancements

• To actively monitor project risks to foresee/identify potential problems and proactively

identify solutions to address in advance

• To ensure the business impact and project objectives/dependencies are identified, always

reported on and managed

• To set up a program, deliver coaching and run projects
• To complete post implementation reviews to ensure successful delivery has been achieved

and to ensure that improvements can be made for future projects

Requirements:

• Minimum of 3 years of experience in the same field or capacity
• Client-Focused Solutions Experience, Project Management Skills, Ability to Communicate

Client Needs with staff

• Excellent understanding of continuous improvement concepts including Six Sigma, Lean

Ideal Skills

• Process Excellence
• Collaboration
• Communication
• Emotional Intelligence
• Open-Mindedness
• Critical Thinking
• Solution Orientation
• Entrepreneurship
• AI Proficiency
• Data Literacy

value stream mapping

• Talent to influence management and ability to manage multiple projects
• excellent written and oral communication skills
• Preferably with either one of the following certifications – COPC, PMP or Lean 6Sigma
• Proficient in the use of Microsoft Office, including Project, Visio, Word, Excel, Outlook, and

PowerPoint

• Experience of the whole project life cycle, able to operate in the initial conceptual design

stage, in the depths of system testing, and at each stage in between

• Stakeholder management skills