We are recruiting a BTS specialist to join our clients Biologics site located in Sligo.  The BTS Specialist is responsible for ensuring that all necessary technical support and administration is provided for all IT / BTS plant systems.  This person will provide end-to-end technical solution support and ensure high availability of IT services for Manufacturing, Lab and supporting functions & areas throughout the site.   Responsibilities: <ul><li>Comply with the companies BTS Road map</li><li>Support of manufacturing and laboratory systems including maintenance and backups.</li><li>Lead Abbvie IT manufacturing systems and application projects</li><li>Participation in cross functional teams and initiatives across the site</li><li>Comply with all corporate policies</li><li>Implementation and updating of all IT policies</li><li>Validation / Qualification of hardware and software</li><li>Liaise with project managers to ensure new product introduction projects meet targets</li><li>Liaise with IT Contractors/Consultants and ensure compliance with contractor management site polices</li><li>Training of employees on relevant applications</li><li>Identify and implement process improvement</li><li>Adheres to and supports all EH&S standards and polices</li></ul>   Education and Experience: <ul><li>Bachelor’s degree in computer science or equivalent relevant discipline required</li><li>3 years plus of relevant IT experience essential</li><li>A minimum of 1 years’ experience in IT manufacturing system / application support role</li><li>Strong organisational and planning skills</li><li>Capability to prioritise and multi-task</li><li>Excellent interpersonal communication skills</li><li>High accuracy and attention to detail</li><li>Excellent teamwork skills</li><li>Initiative and innovation to generate and implement continuous improvements.</li><li>ITIL desirable</li><li>GAMP desirable</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

BTS Specialist

We are currently working with a Leitrim based client who is actively recruitng for a Process Engineer to join their manufacturing plant. Reporting to the Moulding Production Manager, the primary function of this role is to assume responsibility for the control and management of all process driven systems within the Injection Moulding department and direct daily activities in accordance with Company policies. Responsibilities: <ul><li>New tool debug, set up and validation</li><li>Process optimisation using DOE and Statistical Methodology</li><li>Responsible for control of overall quality, process capability, and associated documentation</li><li>Troubleshooting of process, equipment and systems problems using sound engineering principles and data driven decisions</li><li>Provide training and support to Production Technicians</li><li>Root cause analysis and corrective action implementation</li></ul> Qualifications/Requirements:  <ul><li>Degree level qualification in Polymer Science or another relevant Engineering discipline and/or proven equivalent experience</li><li>Strong communication and teamwork skills are essential for this role</li><li>Sound analytical, troubleshooting and problem-solving skills</li><li>Proficient in using a variety of moulding machine types and associated ancillary equipment</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Moulding Process Engineer

Job Purpose The Warehouse Department is part of the Supply Chain function with responsibility for the following areas: Receiving, Material handling and storage, issuance of materials to Production / Packaging and shipping and associated documentation.   Responsibilities: <ul><li>Good Organizational skills</li><li>Ability to make decisions and work on own initiative</li><li>Flexible and adaptable to change</li><li>Computer literate</li><li>Maintain a clean and organized work area</li><li>Assist AbbVie in achieving environmental, health, and safety goals by working safely and observing all general plant and department safety</li><li>Ensure accurate Receipt of Materials in a timely manner</li><li>Ensures that all materials are accurately located and controlled both physically and on SAP.</li><li>Issuance of material to manufacturing and Packaging</li><li>Shipping of product and non-inventory items in accordance with SOPs</li><li>Complete area verification in accordance with SOPs and (ie returns/staging/fixed bins etc)</li><li>Perform all assigned duties according to departmental SOP's and cGMP's.</li><li>Remain current on proper procedures by reviewing current, revised, and new SOP's relating to the job and to the</li><li>Complete and remain current with all required cGMP and safety</li><li>Perform tasks in warehouse that complement the manufacturing and business objectives of the Business units and to provide on-time delivery to customers.</li><li>Complete all required documentation associated with the supply of materials.</li></ul>   Qualifications: <ul><li>Leaving Certificate or equivalent</li><li>3 years + industry experience within a warehouse environment, pharma/regulated environment preferred.</li><li>High sense of safety standards within a regulated GMP environment.</li><li>Experienced computer skills, Outlook, Microsoft Excel. Word & Powerpoint.</li><li>Good Knowledge of SAP and Warehouse processes.</li><li>Experienced forklift driver.</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Warehouse Technician

IT Specialist Job description <ul><li>We are thrilled to offer an exciting opportunity for an experienced IT Specialist to join my Clients growing Team! This is a dynamic, hands-on role that involves a high level of activity and responsibility.</li><li>The position has been created to support the continued growth of the business and the increasing demands on our IT department.</li></ul>Key Responsibilities <ul><li>Provide Tier 2 technical support for desktop hardware, software, and peripherals, ensuring escalated issues are resolved promptly and effectively.</li><li>Collaborate with Tier 1 support teams and internal stakeholders to diagnose and resolve complex desktop-related issues, minimizing disruptions to business operations.</li><li>Monitor and maintain desktop security, implementing best practices and ensuring compliance with organizational policies.</li><li>Assist in planning and executing desktop-related projects and initiatives, aligning with business objectives and technical requirements.</li><li>Manage and support PCs across the network, troubleshooting and resolving computer networking issues efficiently.</li></ul>  Qualifications & Experience <ul><li>Network Infrastructure Devices</li><li>Certifications such as CompTIA A+, Microsoft Certified Professional (MCP), or equivalent are highly desirable.</li><li>Azure Cloud Services</li><li>Active Directory (AD) Administration</li><li>Endpoint Protection Solutions</li><li>VMware Virtualization</li><li>Windows Operating Systems (Installation, Configuration, and Troubleshooting)</li></ul>For a confidential conversation about the role contact Karl on +353 86 201 1223 or klippett@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

IT Systems Engineer

Our client is seeking a skilled and motivated Electrician to join our team. The successful candidate will play a key role in maintaining and improving our manufacturing facilities, ensuring all electrical systems operate efficiently and safely. This is an exciting opportunity to work in a dynamic and high-tech environment. Key Responsibilities 
<ul>
<li>Perform routine maintenance, repairs, and troubleshooting of electrical systems, equipment, and machinery.</li>
<li>Install, test, and commission electrical systems and components in line with company and regulatory standards.</li>
<li>Conduct inspections and preventative maintenance to minimize downtime and ensure optimal equipment performance.</li>
<li>Collaborate with engineering and production teams to identify and implement electrical solutions for process improvements.</li>
<li>Ensure all electrical work complies with Irish electrical regulations and health &amp; safety standards.</li>
<li>Maintain accurate records of maintenance and repair activities.</li>
<li>Assist in energy management and sustainability initiatives.</li>
</ul>
&nbsp; Qualifications &amp; Experience Essential: 
<ul>
<li>Fully qualified electrician with a valid trade certification.</li>
<li>Minimum of 3 years of post-apprenticeship experience, preferably in a manufacturing or industrial setting.</li>
<li>Strong knowledge of electrical systems, schematics, and wiring diagrams.</li>
<li>Familiarity with Irish electrical standards and regulations.</li>
<li>Ability to troubleshoot and resolve complex electrical issues efficiently.</li>
<li>Excellent problem-solving skills and attention to detail.</li>
<li>Proficiency in using electrical testing equipment and tools.</li>
</ul>
&nbsp; Desirable: 
<ul>
<li>Knowledge of Lean Manufacturing principles.</li>
<li>Previous experience in energy efficiency or sustainability projects.</li>
</ul>
&nbsp; Skills &amp; Competencies 
<ul>
<li>Strong communication and teamwork abilities.</li>
<li>Ability to work independently and manage time effectively.</li>
<li>Proactive approach to identifying and addressing potential issues.</li>
<li>Commitment to maintaining a safe working environment.</li>
</ul>
 For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Plant Electrician

The Sterilisation Engineer will play a key role in the development, implementation, and maintenance of sterilisation processes for medical devices. The position supports cross-functional teams, ensuring compliance with industry standards and regulatory requirements while driving process improvements. This technical role requires a solid understanding of engineering principles, including electrical, scientific, and general engineering. Responsibilities: <ul><li>Design, implement, and validate sterilisation processes, ensuring compliance with industry standards and regulatory requirements.</li><li>Develop and execute validation protocols, including IQ/OQ/PQ (Installation, Operational, and Performance Qualification), for both new and existing products.</li><li>Provide technical expertise in sterilisation techniques, material compatibility, and process improvement.</li><li>Troubleshoot and resolve issues related to sterilisation processes and equipment, including implementing corrective and preventive actions (CAPA).</li><li>Maintain and prepare technical documentation, including risk assessments and process validations.</li><li>Serve as the subject matter expert (SME) for sterilisation processes during regulatory audits and inspections.</li><li>Collaborate in design reviews to integrate sterilisation requirements early in the product development lifecycle.</li></ul> Qualifications/Experience: <ul><li>Bachelor’s degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or a related scientific/engineering discipline.</li><li>3–5 years of experience in an engineering role within the medical device or healthcare industry, with a focus on sterilisation processes.</li><li>Proven expertise in sterilisation methods and familiarity with industry standards.</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes.

Sterilisation Engineer

Our client is currently seeking a Quality Control Analyst to join the team Tipperary, Ireland. We offer a range of services, from analytical testing and release to manufacturing our own liquid and oral solid dosage formulations.     Responsibilities: <ul><li>Operate within the lab for the analysis of raw materials, in-process and finished products.</li><li>Perform sampling of materials, utilities and the environment.</li><li>Ensure all operations are conducted in accordance with GMP and good scientific principles.</li><li>Assist in method transfers, method development and validations.</li><li>Review chemical analysis data of raw materials, in-process and finished products.</li><li>Participate in out-of-specification investigations and non-conformance management.</li><li>Administer and manage investigations (e.g. deviations, alarms, OOS).</li><li>Write procedures for QC activities (e.g. SOPs, specifications, test methods, calibration assessments).</li><li>Control and manage stability activities.</li></ul> Requirements/Qualifications: <ul><li>BSc in Life Sciences or equivalent.</li><li>5+ years Pharma or Biotech industry experience within a QC lab.</li><li>Experience with instrument set-up.</li><li>Eligibility to live and work in Ireland</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes.

Quality Control Analyst

Our client is currently seeking an experienced Quality Engineer to join our growing team based in our facility in Shannon, Co. Clare. This organisation has worldwide expertise but also a local presence within our specialized field. This will be a key role in the company and requires someone coming from a fast-paced multi-national company background. The successful candidate will have a minimum of 2-3 years experience in a similar role or environment and have a good working knowledge of ISO9001 and/or AS9100 Quality Management Systems. Excellent interpersonal and communication skills and ability to work under strict time constraints and work well in a pressurized environment. Must be computer literate and experienced in using MS office. Experience of NPI activity is desirable.  Key Responsibilities: <ul><li>Maintaining and updating the QMS documentation/records/systems</li><li>Driving process efficiency, resolving/providing feedback on issues</li><li>Conducting and reporting on internal audits as per annual schedule and closing-out of any non-conformances that arise</li><li>Analysing, identify and implement manufacturing and/or business process improvements which will improve capability performance</li><li>Assisting engineering teams on product/process verification for new and existing products. </li><li>Running CAPA systems and all related tasks. Lead quality problem investigations using proven quality tools.</li><li>Assist with operating and maintaining calibration systems.</li><li>Managing and co-ordination of various quality related projects and quality aspects of production programs</li><li>Provide quality support to operations, including leading and supporting root cause driven approaches to problem solving efforts for quality issues </li><li>Developing and implementing quality controls for new and existing product</li><li>Work individually and within teams on various Quality improvement and efficiency projects </li><li>Provide on-going communication through reports and information transfer as needed</li></ul> Requirements and Skills:   <ul><li>Proven to be self-directed, self-motivated and able to prioritize and resolve competing priorities.</li><li>Strong team member with the ability to identify and drive quality improvements.</li><li>Auditing experience in a manufacturing environment</li><li>Excellent interpersonal and organisational skills</li><li>Excellent verbal and written communication skills</li><li>Good investigative and problem-solving skills with excellent attention to detail</li><li>Decision making capability coupled with the ability to work independently and proactively</li><li>Knowledge and experience of materials, sheet metal and machining processes and or aerospace</li><li>Experience in APQP & PPAP’s would be advantageous</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes.

Quality Engineer

Our client is currently seeking an experienced Health and Safety Officer to join our growing team based in our facility in Shannon, Co. Clare. This organisation has worldwide expertise but also a local presence within our specialized field. This will be a key role in the company and requires someone coming from a fast-paced multi-national company background. Key Responsibilities: <ul><li>Manage the development and strategic implementation of health, safety, and environmental policies and procedures in accordance with current and future relevant legislation and industry best practice.</li><li>Serve as a trusted advisor, providing expert guidance and strategic insights on health and safety matters to internal stakeholders, including senior management.</li><li>Facilitate effective consultation through engagement with Safety Committees and Safety Representatives to drive alignment and consensus.</li><li>Act as an ambassador and promote the development of a positive H&S culture of excellence and inclusion within the organisation.</li><li>Manage  and support/deliver comprehensive HSE training programs, including onboarding, company requirements, procedural updates, and new legal requirements, ensuring all employees and contractors are informed and compliant.</li><li>Lead the compilation and analysis of accident investigation reports, utilizing data-driven insights to support accident prevention initiatives and enhance safety practices throughout the plant.</li><li>Conduct regular audits and risk assessments of work areas, operations and systems; monitor and support corrective and preventative actions.</li><li>Oversee the development and execution of Emergency Plans, including evacuation procedures and drills, to ensure readiness and compliance across all operational areas.Provision of health and safety reports and metrics to Senior Management and administer Health and Safety software systems around document control, auditing, incident reporting etc.</li></ul> Requirements and Skills:   <ul><li>Third level qualification in Health & Safety or similar is required or recognised safety qualification</li><li>At least 2-3 years on-site Safety Officer experience (experience in the manufacturing sector would be an advantage but not mandatory)</li><li>Experience in risk assessment and strong understanding of Irish and EU health and safety legal requirements</li><li>Competent auditor and training experience</li><li>Excellent communication and interpersonal skills with experience in delivering training;</li><li>A self-starter with a proven ability to work on own initiative, with problem solving skills and be innovative;</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes.

Health and Safety Officer

Job Summary: The Validation Engineer will play a critical role in ensuring that all medical devices and associated processes meet quality, regulatory, and performance requirements. This role involves developing and executing validation protocols, conducting testing, and ensuring compliance with industry standards, such as ISO 13485, FDA regulations, and GMP guidelines. Key Responsibilities: <ul><li>Develop, write, and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and software used in medical device manufacturing.</li><li>Perform process validation and re-validation activities to ensure continued compliance.</li><li>Prepare and review validation reports, ensuring clear and accurate records of all testing and findings.</li><li>Maintain detailed documentation of validation activities to support audits and regulatory submissions.</li><li>Ensure all validation processes meet regulatory requirements, including FDA, ISO 13485, and other applicable standards.</li><li>Participate in internal and external audits to demonstrate compliance.</li><li>Perform risk assessments (e.g., FMEA) to identify and mitigate potential issues during validation.</li><li>Analyze test results and provide recommendations for process improvements.</li></ul> Qualifications and Experience: <ul><li>Bachelor’s degree in Engineering (Mechanical, Biomedical, Chemical, or related field) or equivalent experience.</li><li>2+ years in validation engineering within the medical device or pharmaceutical industry.</li><li>Familiarity with regulatory frameworks (e.g., FDA 21 CFR Part 820, ISO 13485).</li><li>Strong understanding of validation processes, including equipment and process validation.</li><li>Experience with quality tools such as FMEA, Root Cause Analysis, and CAPA.</li><li>Proficiency in technical writing and documentation.</li><li>Excellent problem-solving and analytical skills.</li><li>Ability to work independently and as part of a team.</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Niall Finnerty on +35386 1980270/ NFinnerty@sterlingengineeringeu.com

Validation Engineer

Company Overview: Our client is a leading company in the Food & Beverage sector. With ongoing expansion and optimisation initiatives, the company is seeking a skilled Project Controls Engineer to join their team for a 12-month contract role to support key projects, including the installation of new equipment, machine builds, and facility upgrades. Position Overview: The Project Controls Engineer will play a pivotal role in supporting the planning, execution, and delivery of critical projects within the Food & Beverage sector. This includes new equipment installations, machine builds, and working closely with controls teams for seamless project integration. You will also provide ongoing front-line shop support and ensure that projects are managed through their entire life cycle—from design and implementation through to commissioning and handover. Key Responsibilities: <ul><li>Project Planning & Scheduling: Develop, manage, and maintain project schedules, particularly for new equipment installations, machine builds, and process optimizations. Use tools like MS Project, Primavera P6, or SAP to ensure projects are delivered on time.</li><li>Cost Control & Budget Management: Monitor project budgets, manage cost forecasts, track expenditures, and recommend actions to control costs. Ensure that project costs are within scope and align with budget expectations.</li><li>Equipment & Machine Builds: Oversee and manage the installation of new machinery and equipment, ensuring projects meet quality, timeline, and budget expectations. Coordinate with engineering teams for design, procurement, and installation phases.</li><li>Collaboration with Controls Teams: Work closely with controls engineers, automation teams, and electrical contractors to ensure that control systems are correctly designed and integrated into new machines and processes.</li><li>Front-Line Shop Support: Provide direct support to the shop floor to resolve any operational or technical challenges. Ensure smooth integration of new equipment and provide troubleshooting support to manufacturing teams.</li><li>Project Life Cycle Management: Manage all phases of the project life cycle, including feasibility, design, procurement, installation, testing, and commissioning. Ensure that projects are completed to required specifications, regulatory standards, and operational readiness.</li><li>Risk Management: Proactively identify project risks, develop risk mitigation strategies, and ensure proper documentation of risks and issues. Maintain focus on minimizing delays and cost overruns.</li><li>Reporting & Documentation: Prepare regular project status updates for management and stakeholders. Document key decisions, scope changes, and project milestones.</li><li>Stakeholder Communication: Liaise with project managers, engineering teams, external contractors, and senior stakeholders to ensure alignment and resolution of issues that may arise during the project execution phase.</li><li>Change Control: Implement and manage project changes in scope, schedule, and cost, ensuring that all changes are approved and documented according to the company’s change control procedures.</li><li>Post-Project Review & Handover: Ensure that all projects are successfully closed out, with appropriate documentation provided to operations teams for long-term support.</li></ul> Qualifications and Experience: <ul><li>Bachelor’s degree in Engineering, Project Management, or a related field.</li><li>3+ years of experience in project controls, ideally in a manufacturing environment with hands-on experience in new equipment installations, machine builds, and controls systems integration.</li><li>Strong background in project planning and scheduling with tools like MS Project, Primavera P6, or SAP.</li><li>Experience with project life cycle management, from design through commissioning and operational handover.</li><li>Knowledge and experience working with controls teams, automation engineers, and electrical contractors to ensure seamless integration of new systems and machinery.</li><li>Strong experience providing front-line shop floor support, particularly in troubleshooting machine or equipment-related issues during installation and operational integration.</li><li>Cost control and budget management experience, including preparing cost forecasts and variance analysis.</li><li>Familiarity with food & beverage manufacturing processes and understanding of relevant industry standards and regulations.</li><li>Experience with risk management and change management in a project environment.</li><li>Proficiency in Excel and other data management tools for project performance tracking.</li></ul> Desirable Skills: <ul><li>Certification in Project Management (e.g., PMP, Prince2).</li><li>Experience in the Food & Beverage or Pharmaceutical industries, especially in equipment installations and machine builds.</li><li>Familiarity with Lean Manufacturing, Six Sigma, or continuous improvement methodologies.</li><li>Working knowledge of automation controls systems, including PLCs, SCADA, or DCS systems.</li></ul> If you are a Project Controls Engineer with experience in machine builds, equipment installations, and project life cycle management, we invite you to apply and join us for this exciting 12-month contract opportunity in Mayo.

Project Controls Engineer

Company Overview: Our client, a leading Medical Device company based in Galway, is dedicated to delivering high-quality medical solutions that improve patient outcomes. The company is committed to innovation and excellence, and they are seeking a talented E&I Instrumentation Engineer to join their growing team. The successful candidate will play a critical role in maintaining and enhancing the electrical and instrumentation systems used in the production of life-saving medical devices. Position Overview: As an E&I Instrumentation Engineer, you will be responsible for the maintenance, troubleshooting, and optimization of electrical and instrumentation systems within a highly regulated environment. You will work closely with cross-functional teams to ensure that all instrumentation systems are operating efficiently, reliably, and in compliance with regulatory standards. This role requires a strong background in electrical and instrumentation engineering, with experience in the medical device or regulated industries. Key Responsibilities:<ul><li>Instrumentation Maintenance: Maintain and troubleshoot instrumentation systems (e.g., sensors, actuators, control systems) to ensure optimal functionality and performance.</li><li>System Calibration: Perform calibration, validation, and qualification of instrumentation and electrical systems in accordance with FDA, ISO, and other regulatory standards.</li><li>Compliance & Documentation: Ensure all activities comply with industry standards and regulations (e.g., ISO 13485, FDA 21 CFR Part 820). Maintain accurate records of maintenance activities, calibration data, and system changes.</li><li>Project Support: Support new equipment installations, upgrades, and system modifications. Provide technical support for the design, testing, and validation of new instrumentation systems.</li><li>Root Cause Analysis: Perform root cause analysis (RCA) for instrumentation-related issues and implement corrective and preventive actions (CAPA).</li><li>Collaboration: Work with manufacturing, quality, and automation teams to ensure seamless integration and operation of electrical and instrumentation systems.</li><li>Continuous Improvement: Identify opportunities for process improvements and efficiency gains in electrical and instrumentation systems.</li><li>Training & Support: Provide training and technical support to operations and maintenance personnel on instrumentation systems and procedures.</li></ul> Qualifications & Experience: <ul><li>Bachelor's degree in Electrical Engineering, Instrumentation, Automation, or a related field.</li><li>3+ years of experience in an instrumentation engineering role, ideally within the medical device or regulated industries (pharmaceutical, biotechnology, etc.).</li><li>Solid understanding of electrical systems, control systems, and instrumentation (e.g., PLCs, SCADA, DCS, sensors, actuators, etc.).</li><li>Experience with GxP environments and regulatory compliance (FDA, ISO, etc.).</li><li>Knowledge of control system architectures, analog and digital signals, and instrumentation design.</li><li>Proficient in AutoCAD, PLC programming, LabVIEW, or other relevant software tools.</li><li>Strong troubleshooting and analytical skills with a proactive approach to problem-solving.</li><li>Excellent written and verbal communication skills.</li></ul> Desirable Skills:<ul><li>Experience with SCADA or DCS systems.</li><li>Project management experience in regulated industries.</li><li>Familiarity with Risk Management processes (e.g., FMEA).</li><li>Six Sigma or Lean Manufacturing experience.</li><li>Certified Automation Professional (CAP) or similar certifications.</li></ul>

E&I Instrumentation

Role: We are recruiting on behalf of a client in Sligo seeking an EHS Specialist for their medical device manufacturing site. This role is on a contract basis and focuses on contractor management, daily EHS activities, and ISO standards compliance, with significant involvement in environmental licensing and sampling/compliance management Responsibilities: <ul><li>Policy & Compliance: Ensure adherence to all company policies, standards, site procedures, and regulatory requirements.</li><li>Incident Management: Assist in incident and accident investigations, providing EHS support for change management processes.</li><li>Documentation & Procedures: Prepare, implement, and review EHS procedures to align with site activities and ensure regulatory compliance.</li><li>Risk & Safety Analysis: Provide technical support for risk assessments and Job Safety Analysis (JSA) programs on site.</li><li>Metrics & Reporting: Gather and report EHS metrics and Key Performance Indicators (KPIs).</li><li>Training & Audits: Develop and deliver EHS training programs, conduct routine walkdowns, audits, and program reviews to maintain compliance with safety and environmental standards.</li></ul>Requirements <ul><li>Education: Bachelor’s degree in EHS, Science, Engineering, or related discipline.</li><li>Experience: Ideally a minimum of 2 years experience in an EHS role within a regulated environment.</li><li>Technical Skills: Proficiency in Microsoft Office (Word, Excel, PowerPoint); knowledge of ISO 14001 and ISO 45001 systems.</li><li>Competencies: Strong communication, analytical, and problem-solving skills with a proactive approach and sound judgment.</li><li>Multitasking & Organisation: Ability to manage multiple tasks efficiently in a dynamic environment.</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes.

EHS Specialist 

The role: The QA Validation Specialist will be responsible for the delivery of Quality Assurance activities to ensure the product is manufactured in accordance with GMP and Regulatory requirements. The role will also include the review and approval of validation documentation and activities related to the qualification of the facility, equipment, and utilities to support start-up and on-going manufacturing. This role will be a key member of the Quality Assurance team, providing hands-on technical support and oversight for validation activities at the manufacturing facility. This role is essential in ensuring that processes and equipment are validated and qualified according to industry regulations while guiding the implementation of the Site Validation Master Plan. This key role is an individual contributor role whereby the individual must be a self-starter with professional and academic experience in QA and Validation activities. This key role must ensure effective interaction with other departments such as Quality Control, Manufacturing, Engineering and Technical Services.   Responsibilities: <ul><li>Site QA point of contact providing technical expertise, feedback and guidance for QA and compliance topics /issues including validation strategy /approach, new product introduction and manufacturing and assist in the resolution of issues commensurate with the level of risk.</li><li>Review and approval of validation documentation and activities related to the qualification of the facility, equipment, and utilities to support start-up and on-going manufacturing.</li><li>Manage assigned areas of Quality Management System (QMS) to ensure the manufacture of product in accordance with GMP and regulatory requirements.</li><li>QMS areas of responsibility include Deviation investigations, Change Control and CAPA management systems; Internal/External audits; Vendor Management; review /approval Manufacturing Batch Records and assessment /approval of production materials.</li><li>Generate, review, and approve SOP's/other documentation as applicable to your areas of responsibility.</li><li>Perform timely review and approval of site procedures and documentation to ensure compliance with GMP and regulatory requirements.</li><li>Ensure schedules for review and approval of GMP /validation documents are maintained to support technology transfers and new product introduction project timelines.</li><li>Ensure application of Quality Risk Management principles including the application of risk assessment tools such as FMEA</li><li>Act as the QA lead in QA activities in project work-streams involving cross-functional, multidepartment teams including Operations, Quality Control, Quality Assurance, Engineering, and others.</li><li>Actively contribute to continuous improvement activities.</li><li>Other duties as assigned.</li></ul>  Requirements: <ul><li>Third level qualification in relevant science and/or engineering discipline</li><li>5 years minimum experience working in a in a GMP Quality environment providing QA technical support and oversight to validation and qualification activities </li><li>Experience in a Validation function with strong knowledge of Project Life Cycle and cGMP Regulations</li></ul> Core Competences <ul><li>Strong understanding of GMP compliance and quality standards</li><li>In-depth knowledge of quality management system (QMS) procedures and technical documentation</li><li>Excellent analytical, problem-solving, and decision-making skills</li><li>Excellent attention to detail and significant document review experience essential</li><li>Excellent technical writing skills including deviation reports and SOPs</li><li>Demonstrate ability to drive the completion of tasks, trouble shooting skills and excellent attention to detail</li></ul>

QA Specialist (Validation)

We are seeking an experienced Senior Quality Manager to oversee the Quality Assurance function within our clients Limerick-based medical device manufacturing facility. This role will be instrumental in ensuring product quality and compliance with regulatory requirements, driving continuous improvement, and leading quality initiatives. The successful candidate will manage a team of quality professionals, work cross-functionally to embed quality into all processes, and ensure that products meet the highest standards of safety and efficacy. Key Responsibilities <ul><li>Quality System Management: Oversee and maintain the Quality Management System (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, MDR, and other relevant standards and regulations.</li><li>Regulatory Compliance: Ensure that all quality assurance activities are in full compliance with regulatory requirements, including documentation, audits, and submissions.</li><li>Audit Management: Lead internal and external audits, including FDA, Notified Body, and customer audits. Address findings promptly, ensuring that corrective and preventive actions (CAPAs) are effectively implemented.</li><li>Team Leadership and Development: Manage, mentor, and develop the quality assurance team, fostering a culture of quality, accountability, and continuous improvement.</li><li>Risk Management: Implement and oversee risk management activities, including Failure Mode and Effects Analysis (FMEA) and risk assessments, ensuring the consistent identification and mitigation of quality risks.</li><li>Supplier Quality: Develop and manage supplier quality programs, conduct supplier audits, and implement quality agreements with suppliers to ensure incoming materials meet specified quality standards.</li><li>CAPA Management: Oversee the CAPA process, ensuring timely investigation, root cause analysis, and implementation of corrective actions, with a focus on reducing recurrence.</li><li>Product Life-cycle Support: Provide quality support across product life-cycle stages, including new product development, manufacturing, and post-market surveillance.</li><li>Process Improvement: Drive continuous improvement initiatives to optimise quality processes, reduce product defects, and improve manufacturing and operational efficiency's.</li><li>Customer and Complaint Handling: Oversee complaint investigations, trend analysis, and customer feedback processes, ensuring timely resolution and compliance with regulatory reporting requirements.</li><li>Data Analysis and Reporting: Develop and monitor key quality metrics (KPIs), prepare quality reports, and present findings and improvements to senior management.</li></ul> Essential Qualifications and Skills <ul><li>Education: Bachelor’s degree in Engineering, Life Sciences, Quality, or a related field. Advanced degree (e.g., Master’s or Ph.D.) is an advantage</li><li>10+ years of experience in quality assurance within the medical device or related regulated sector, with at least 5 years in a managerial role.</li><li>Strong understanding of ISO 13485, FDA 21 CFR Part 820, MDR, and other applicable regulations and standards.</li><li>Demonstrated success in managing a Quality Management System in a highly regulated environment.</li><li>Proven experience in managing internal and external audits, CAPA processes, and supplier quality management.</li></ul> Technical Skills: <ul><li>Proficiency in quality management tools, including QMS software, statistical analysis tools, and risk management methods.</li><li>Familiarity with process validation, design control, risk management techniques (e.g., FMEA), and root cause analysis tools.</li><li>Strong knowledge of product life-cycle quality, including experience with post-market surveillance and complaint handling.</li></ul> Soft Skills: <ul><li>Strong leadership skills with a proven ability to lead and motivate a team.</li><li>Excellent communication and presentation skills for cross-functional collaboration and stakeholder reporting.</li><li>Analytical mindset with attention to detail and the ability to identify and implement improvement opportunities.</li></ul> Preferred Qualifications <ul><li>Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or other relevant quality certifications (e.g., Six Sigma, ASQ).</li><li>Experience in Lean Manufacturing, Six Sigma, or similar methodologies for process improvement.</li></ul>Familiarity with regulatory submission requirements for the medical device industry. What We Offer <ul><li>Competitive salary and comprehensive benefits package.</li><li>A collaborative work environment with opportunities for advancement.</li><li>Support for continuous professional development and training.</li><li>Involvement in meaningful work that positively impacts patients and healthcare.</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Niall Finnerty on +35386 1980270/ NFinnerty@sterlingengineeringeu.com

Senior Quality Manager

The role: Our client is seeking an experienced Staff EHS Specialist to join their medical device manufacturing plant based in Limerick. Responsibilities: <ul><li>Ensure compliance with all health, safety, and environmental regulations, standards, and company policies.</li><li>Conduct regular risk assessments, site inspections, and audits to identify hazards and implement corrective measures.</li><li>Develop and deliver HSE training programs for employees and contractors; conduct comprehensive site inductions.</li><li>Lead investigations into incidents, accidents, and near misses, implementing corrective actions to mitigate reoccurrence.</li><li>Develop, test, and maintain emergency response plans through drills and simulations.</li><li>Monitor and manage environmental aspects, promoting sustainability and ensuring compliance with environmental regulations.</li><li>Maintain HSE documentation, including risk assessments, incident reports, and training records, ensuring accuracy and currency.</li><li>Communicate HSE policies and procedures effectively across all levels of the organization, fostering a culture of safety.</li><li>Stay current on changes in HSE legislation, ensuring alignment of company practices with up-to-date standards.</li></ul> Requirements: <ul><li>Bachelor’s degree in Occupational Health & Safety, Environmental Science, or a related discipline.</li><li>Minimum of 3–4 years of experience in an HSE role.</li><li>Strong knowledge of Irish health, safety, and environmental legislation, with a track record of successfully implementing HSE programs and policies.</li></ul> For a confidential conversation about the role contact Owen Clancy at +353 86 060 2922 or oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes.

Senior Staff EHS Specialist

Responsible for providing technical leadership to solving technical problems for the operations team. A core element of the role is to manage the development of the engineering competencies with direct reports, and also the remaining operations engineers in the Limerick facility. The role will involve developing engineering best practice and coaching and mentoring operations engineers on engineering best practice.  Duties: <ul><li>Be responsible and accountable for the development of the best engineering strategy to deliver the Operational objectives of the Limerick business units. </li><li>Work in harmony with the Operations managers and Quality leaders to provide leadership and a consistent focus on product and process quality.  </li><li>Lead a team of assigned engineers and other functional professionals to deliver specific project objectives which support the operations strategy. </li><li>Work closely with the Limerick Operations Management team to ensure optimum business results in the short, medium and long term. </li><li>Be responsible to manage the engineering competencies of assigned engineers and partner with the Operations managers to ensure consistent development across the business unit ME’s. </li><li>Develop and complete IDP’s and performance reviews with assigned engineers to provide structured development opportunities to improve performance and engagement. </li><li>Be responsible, (with others) for the design and continuous development of the engineering Competency Management Process; be a member of the Engineering Competency certification board.</li><li>Liaise with other function leaders where appropriate to ensure the engineering teams comply with and support cross functional best practice in GMP’s, GDP’s, Finance Processes, Compliance Initiatives and EHS Requirements. </li></ul> Qualifications: Required: <ul><li>An Honours Degree (Level 8) in an Engineering discipline.</li><li>5 years relevant experience in a technical engineering role with a minimum of 3 years’ experience within manufacturing operations.</li></ul> Preferred: <ul><li>A qualification in Lean Manufacturing.   </li><li>Business understanding of operations and their impact is essential. </li><li>A demonstrated ability to coach and guide others and strong communication skills. </li><li>A demonstrated ability to facilitate a team of engineers to deliver a specific objective. </li><li>Strong project management skills. </li><li>Self-starter with demonstrated efficient work methods, analytical & problem solving skills  </li><li>Capable of working as part of a multi-disciplined team</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Gerard Cunniffe on +353 86 190 8885. ''

Associate Engineering Manager

The Automation and Controls Engineer will provide technical support for the site in the field of automation. They will proactively resolve technical issues and collaborate as part of the wider engineering team in the delivery of continuous improvement initiatives and strategic manufacturing improvements. Duties: <ul><li>Provide frontline support to operations for Automation and Controls components within the manufacturing process. </li><li>Identify, evaluate & implement opportunities for continuous improvement.</li><li>Provides support in the selection of new technologies to improve plant efficiencies.</li><li>Participates within project teams, provides technical support and makes informed decisions on hardware and architecture selection.</li><li>Proactively resolve technical issues before they impact business priorities.</li><li>Analyse, understand, fault-find and modify where necessary automation software in line with the sites quality management system.</li><li>Under supervision develop, test, and install control’s software as part of a highly automated and validated production environment.</li><li>Work within a cross functional multi-discipline team environment.</li><li>Ability to use data and metrics to anticipate problems and make data driven decisions in response.</li><li>Support the wider engineering team in completion of project delivery tasks assigned.</li><li>Provide on the job training/support to new team members as required.</li><li>All other duties as assigned.</li></ul>Qualifications: <ul><li>Level 8 Degree in Electrical/Electronic Engineer, Computer Science or related field with equivalent technical experience is required.</li><li>Has 0-2 years’ experience in a manufacturing environment.</li><li>Demonstrated ability to provide technical solutions for complex problems through automation and controls knowledge.</li><li>Working knowledge of PLC and HMI control systems is essential.</li><li>Experience with Allen Bradley and Siemens controls systems would be advantageous.</li><li>Basic understanding of ISA95 and ISA88 design/implementation principles.</li><li>Strong communication and influencing skills with both internal and external stakeholders.</li><li>Capable of working autonomously or as part of a multi-disciplined team in an aggressive, dynamic and results motivated environment.</li><li>A team player, with a flexible approach.</li><li>Must be willing to source, investigate and implement technological and automation advances.</li><li>Experience in an FDA regulated or regulated industry beneficial.</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Gerard Cunniffe on +353 86 190 8885.

Automation & Controls Engineer

Galway €80,000 / €90,000 DOE I am excited to present an opportunity to join a dynamic and forward-thinking team in a fast-paced, evolving market. This role offers the chance to innovate, collaborate with cutting-edge technology, and work in alignment with industry best practices. This is an excellent career opportunity for anyone looking to work on various projects and expand their experience in leading in the embedded firmware space. The successful candidate will have a demonstrated interest in firmware development and design, will thrive on the challenges of learning new technologies in a fast-paced environment and enjoys working as part of a highly skilled and project orientated team. Experience & Qualifications: <ul><li>Experience in leading a Firmware Team</li><li>Proven experience developing and debugging multi-threaded systems</li><li>Linux/C programming skills experience required along with a relevant 3rd level qualification.</li><li>Understanding of UNIX/Linux operating systems and programming environments.</li><li>Developing and testing code using strict development methodologies including unit test driven development, code reuse, maintainability, testing and documentation.</li></ul>Desirables: <ul><li>Linux Kernel and/or driver development</li><li>Unit Test driven development</li><li>Bluetooth classic or BLE development</li><li>Experience with GSM AT Commands / Modem integration</li><li>GPS/Positioning</li></ul>

Lead Firmware Engineer

Dept: QC Pharma Reports to: Quality Lab Supervisor Location: Westport   Responsibilities <ul><li>Perform Chemistry analysis of In process / Final product as per schedule and in accordance with regulatory requirements. Also perform analysis on Stability samples from a wide range of products</li><li>Documenting all testing activities, results and raw data on time, accurately and legibly</li><li>Use of laboratory IT systems including LIMS and Empower</li><li>Reviews and interprets test results</li><li>Adhering to all company standards in the areas of safety, housekeeping and quality, notifying management of any discrepancies</li><li>Ensure good housekeeping and good laboratory practices</li><li>Rotating shifts monthly</li><li>Work with team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance to Quality Management System</li></ul>Education and Experience/Knowledge: <ul><li>3rd Level Qualification in a Science Discipline, preferably Chemistry related.</li><li>1-2 Years’ experience working as an Analyst in a GMP/GLP environment.</li><li>1-2 Years’ experience of working with a range of Analytical Equipment specifically HPLC and GC and well as other laboratory techniques.</li><li>Experience and good knowledge of Empower.</li><li>Good knowledge and understanding of Data Integrity from Laboratory perspective.</li><li>Excellent communication, organization, time-management and teamwork skills</li><li>Demonstrate ability to work on one’s own initiative</li></ul>

Laboratory Technician

Shannon We are now seeking a highly skilled and motivated Program Manager to join our dynamic team. The Program Manager will be responsible for overseeing and managing the portfolio of projects within our Product Development Department, ensuring that they are completed on time, within budget, and meet quality standards. Job Highlights: <ul><li>Establishing Project Management Processes: You'll introduce and customize project management best practices, ensuring a uniform approach across all projects from concept to high-volume manufacturing.</li><li>Comprehensive Project Planning: The role involves developing and managing detailed project plans, covering all phases—objectives, resources, timelines, and deliverables—to ensure successful project execution.</li><li>Resource Management: The position focuses on optimizing resource allocation through effective work estimation and capacity planning, maintaining alignment with budget and project demands.</li><li>Stakeholder & Risk Management: You'll handle the expectations of multiple stakeholders, develop risk mitigation strategies, and ensure seamless communication to keep projects aligned with organizational goals.</li><li>Budget and Quality Oversight: Monitoring project budgets, ensuring quality control, and aligning deliverables with client requirements are crucial to this role.</li><li>Team Leadership: Fostering a collaborative work environment, guiding cross-functional teams, and driving continuous improvement will be integral to ensuring project success.</li></ul> Ideal Candidate Profile: <ul><li>Education & Experience: A degree in Engineering or Project Management, with at least five years of experience, ideally in electronics or a related sector, is essential.</li><li>Project Management Expertise: Knowledge of Agile, Waterfall, and other methodologies, coupled with proficiency in tools like Microsoft Project or Jira, is necessary for managing complex projects.</li><li>Leadership & Communication Skills: Strong interpersonal skills for managing diverse teams and stakeholders, paired with leadership experience, will be critical for success.</li><li>Technical & Analytical Aptitude: Familiarity with high-volume manufacturing is a plus, alongside a strong ability to analyze project data, solve problems, and make informed decisions.</li><li>The role offers an excellent opportunity to shape the future of product development and innovation within one of Ireland’s leading electronics firms, driving both strategy and execution across the department.</li></ul>   By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Tommy McKeown on +35386 2044918/ tmckeown@sterlingengineeringeu.com

Program Manager

Location: Shannon Salary: €60,000 DOE Working as part of the Test Engineering team the Test Engineer will be responsible for the design, assembly, and support of Test Equipment for use in new and existing production lines. They will leverage their electronics and NI LabVIEW knowledge and expertise to deliver Test equipment that will ensure our clients products perform as required in the field. Key responsibilities include: <ul><li>Contribute to the Design, Development & Assembly of Test Equipment for use with new and existing Fire and Gas detection products.</li><li>Test software development.</li><li>Project Management</li><li>Interdepartmental collaboration on product design and test requirements</li><li>Support escalated hardware and software fault finding / trouble shooting of existing automated high-volume manufacturing test equipment.</li><li>Documentation of designed Circuits and Procedures.</li></ul>The Person We are looking for: <ul><li>Third Level Qualification in Electronic Engineering or equivalent experience</li><li>2+ years relevant experience in high volume manufacturing environment.</li><li>Digital and analogue electronics knowledge and experience.</li><li>Familiarity with In-Circuit Test Equipment (desirable but not essential)</li><li>Test software development experience. Labview experience is desirable, or willingness to undertake</li><li>LabView training.</li><li>RF knowledge and experience (desirable but not essential)</li><li>Familiarity with Microsoft office programs such as Outlook, Word & Excel</li><li>Excellent verbal and written communication skills</li><li>A high level of energy and enthusiasm with a strong work ethic.</li><li>Flexible, adaptable with a positive attitude</li><li>Ability to work autonomously or as part of a Team.</li><li>Demonstrated problem-solving skills.</li><li>Ability to work under pressure and meet agreed delivery schedules.</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Niall on +353 86 1980270

Embedded Engineer

Project Engineer - Contract Sligo Primary Responsibilities: <ul><li>To provide Engineering services to the plant, in order to maximise the availability of all Site Process Equipment and Utilities.</li><li>To manage capital engineering projects (typical project value range: anything up to €5 million).</li><li>To support the engineering teams in controlling uptime of process equipment and optimizing efficiencies both in equipment and process performance.</li><li>To support the Engineering team with the emphasis on continual operational improvements.</li><li>To provide process engineering support and technical trouble shooting within the site.</li><li>To improve the operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives.</li><li>To manage the execution of projects within the engineering group including specific Process Safety Projects.</li><li>To support the provision of process safety initiatives to the site.</li><li>To liaise with Production to ensure equipment performance is maximized.</li><li>To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining, troubleshooting and installing/commissioning equipment.</li><li>To provide engineering support and technical trouble shooting to all site operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives.</li><li>Leadership of process equipment commissioning and validation activities.</li><li>Identification and project management of continuous improvement projects.</li><li>Work closely with all site functions and other departments to deliver these continuous improvement projects.</li><li>Preparation of feasibility studies and budget management for all assigned projects.</li><li>Management and negotiation of external contracts and contractors.</li><li>Support all major site initiatives and sites core goals.</li></ul>Requirements/Qualifications: <ul><li>Degree in a relevant Engineering Discipline.</li><li>Strong pharmaceutical experience is essential.</li><li>Must have demonstrated relevant site experience of one or more of the below: o API process equipment trains (reactors, filter dryers, pumps, process pipework, milling, containment technology – gloveboxes, downflow booths, etc). o Drug Product equipment (tablet press, roller compaction, tablet coater, material handling – post hoists, blenders, milling – Quadro Comils, etc) o Cleanroom processing/utilities – HVAC, CIP systems, Purified water generation and distribution systems, etc.</li><li>Knowledgeable/competent with executing change control.</li><li>Experience in process engineering, with relevant experience of batch processing, automation, project management, commissioning and validation, equipment reliability and continuous improvement.</li><li>Working knowledge of distributed control systems, such as Delta V.</li><li>This is a hand-on role requiring a logical and structured approach to resolving day to day engineering issues typical of a live manufacturing environment.</li><li>Knowledge of cGMP and regulatory requirements relating to the Healthcare industry is required.</li><li>Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements.</li></ul>Desirable Requirements: <ul><li>Trackwise change control system experience</li><li>Electrical background – competency with electrical system design & installation (process equipment and site electrical infrastructure), familiar with ATEX regulations and requirements.</li></ul>  By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Gerard Cunniffe on +35386 190 8885 / gcunniffe@sterlingengineeringeu.com

Project Engineer

Senior Automation Engineer Dundalk - Can also be located in Limerick. Salary: DOE - €55,000/85,000 Our Client produce high quality automation solutions that impacts on the execution of real-world machinery and processes. Our automation enables autonomous aqua drones to navigate the seas, robots to assemble complex products, pharmaceuticals to produce life-changing medicines. Our Client are a fast-growing company with great career opportunities, an ideal candidate would want to grow with them and have the vision of building the automation machines and solutions of the future. They are looking for a highly motivated, result-driven and confident Senior Automation Engineer.   As a Senior Automation Engineer, your role will be the development, commissioning and support of automation control systems across a wide spectrum of industries utilising cutting edge technologies. You will be responsible for system designs, standard library roadmap’s, specifications, programming, simulation, testing and overseeing commissioning. The candidate must possess the technical expertise to maintain, develop, troubleshoot and validate these systems in a compliant manner. Responsibilities: <ul><li>Manage the specification, development, installation and validation of automation projects within budget and corporate guidelines.</li><li>Software development of bespoke machines & manufacturing systems.</li><li>Interact with the customers on technical requirements.</li><li>Assess existing technologies and processes.</li><li>Design and deliver best in class automation solutions.</li><li>Work within a team and upskill junior engineers.</li><li>Document the project and manage change control.</li><li>Work independently and manage multiple tasks under tight deadlines.</li><li>Ability to take ownership of projects.</li></ul>  Qualifications: <ul><li>Third level qualification in Automation, Electrical, Mechanical, Electronic, Computer Science</li><li>5+ Years industry experience</li><li>Industry experience with preference for Rockwell Studio 5000, FT View, Ignition, Siemens TIA Portal/Step7, OSI PI Historian, VBA.</li><li>Knowledge of 21 CFR Part 11 and GAMP an advantage</li><li>Cisco Networking qualification and or VMware or equivalent qualification an advantage</li><li>Knowledge of Robotics and safety standards an advantage</li><li>Thorough knowledge of automation principles and procedures</li><li>Ambitious, confident and professional individual with strong communication and organisational skills</li></ul> Renumeration package to reflect experience and qualifications. By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Gerard Cunniffe on +353 86 190 8885.

Snr Automation Engineer

Purpose An engineering professional who, working with little or no supervision, applies advanced scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete complex assignments related to one or more technical fields or disciplines. Contributes to the development of new principles and concepts.   Responsibilities <ul><li>Prepare agenda and reports for PMO meetings to ensure awareness of project progress and issues of interest to the Global Packaging team</li><li>Supports department Long Range Plan (LRP) and Capital Plan submissions by analysing projects for accuracy and detail</li><li>Serves as department spokesperson on projects and/or programs. Acts as advisor to management and customers on advanced technical research studies and applications.</li><li>Ensures awareness of project status and issues. Develops and presents project updates.</li><li>Acts as the system owner for the PMO portfolio SharePoint application.</li><li>Write project justifications (Request for Capital Expenditure),including savings analysis that may be generated with the investment. Initiate capital project ideas dealing with safety and quality improvement, capacity increase, and/or cost reduction.</li><li>Supports department Long Range Plan (LRP) and Capital Plan submissions by analysing projects for accuracy and details.</li></ul>  Qualifications <ul><li>A Bachelors Degree in Engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 5+ years of significant engineering and/or operational experience.</li><li>Has demonstrated excellence in breadth and depth within discipline and across disciplines.</li><li>Interacts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators.</li><li>Strong Project Management skills</li><li>Listens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations.</li><li>Works well with other engineers in a collaborative, fast-paced goal-driven environment.</li><li>Strong presentation and management communication skills</li><li>Possesses interpersonal skills to negotiate and reconcile differences.</li><li>Strong meeting collaboration skills. Interacts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators.</li><li>Has a technical background in health care, medical devices, pharmaceutical, biologics, or similar industries (preferred).</li><li>Has demonstrated competency with financial systems and in fiscal control.</li><li>Computer literacy and proficiency in Microsoft Office applications (Word, Outlook, Excel, PPT)</li></ul>By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Owen Clancy on +353 86 060 2922.

Position: Test Engineer Location: Shannon Working as part of the Test Engineering team the Test Engineer will be responsible for the design, assembly, and support of Test Equipment for use in new and existing production lines. They will leverage their electronics and NI LabVIEW knowledge and expertise to deliver Test equipment that will ensure  our client'sproducts perform as required in the field. Key responsibilities include: <ul><li>Contribute to the Design, Development & Assembly of Test Equipment for use with new and existing Fire and Gas detection products.</li><li>Test software development.</li><li>Project Management</li><li>Interdepartmental collaboration on product design and test requirements</li><li>Support escalated hardware and software fault finding / trouble shooting of existing automated high-volume manufacturing test equipment.</li><li>Documentation of designed Circuits and Procedures.</li></ul> We are looking for: <ul><li>Third Level Qualification in Electronic Engineering or equivalent experience</li><li>2+ years relevant experience in high volume manufacturing environment.</li><li>Digital and analogue electronics knowledge and experience.</li><li>Familiarity with In-Circuit Test Equipment (desirable but not essential)</li><li>Test software development experience. Labview experience is desirable, or willingness to undertake</li><li>LabView training.</li><li>RF knowledge and experience (desirable but not essential)</li><li>Familiarity with Microsoft office programs such as Outlook, Word & Excel</li><li>Excellent verbal and written communication skills</li><li>A high level of energy and enthusiasm with a strong work ethic.</li><li>Flexible, adaptable with a positive attitude</li><li>Ability to work autonomously or as part of a Team.</li><li>Demonstrated problem-solving skills.</li><li>Ability to work under pressure and meet agreed delivery schedules.</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Niall Finnerty on +353 86 1980270.

Test Engineer

Position: Environmental Specialist Type: 6 month FTC - rolling Location: Limerick Rate: Depending on experience Duties: <ul><li>Monitors the environmental program to ensure compliance with IPC Licence</li><li>Compile and submit all regulatory reporting requirements to the EPA within the specified timeframes</li><li>Act as the site’s Environmental contact for the EPA</li><li>Act as the lead on-site environmental contact for all onsite Environmental Audits (both internal & external)</li><li>Report immediately to Senior EHS Manager/ Director any Environmental compliance incidents on site.</li><li>Lead and/or support the investigation of any Environmental incidents /noncompliance events on site.</li><li>Provide DGSA support to the site and act as the environmental lead for onsite DGSA audits.</li><li>Compile and submit all EPA Reports</li><li>Manages / coordinates all Environmental monitoring/sampling on site and analyses and documents all associated results.</li><li>Act as the main point of contact for all on site waste management issues</li><li>Develop, maintain on site environmental documentation, and deliver training programs to ensure environment compliance where applicable.</li><li>Implement ISO 14001: 2015</li><li>Lead the Radiation Protection Program</li><li>Monitoring environment regulations to ensure compliance readiness .</li></ul> Essential : <ul><li>Environmental Science / Engineering Degree or equivalent</li><li>A minimum of 3 years' professional experience required in environment, health, and safety programs.</li><li>A minimum of 2-3 years relevant experience in an EPA regulated facility and in a cGMP environment is desirable</li><li>Knowledge and understanding of environment regulations.</li><li>Knowledge and understanding of environment compliance reporting.</li><li>Specific experience in hazardous waste management or other professional EHS trainings or certifications a plus.</li></ul> Additional Skills: <ul><li>Ability to make effective oral presentations and work as part of a team.</li><li>Proficiency in organizing, communication, problem solving, multitasking and collaborating with others.</li><li>The individual in this position will be able to organize his/her own work on a routine basis. The individual must be able to provide updates and tracking on tasks.</li><li>Good communication skills required, both verbal and written.</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Gerard Cunniffe on +353 86 190 8885.

Environmental Specialist / Limerick / FTC

Role Summary:  The Validation Engineer will play a crucial role in the QA department, reporting directly to the Head of Quality. This position involves reviewing and issuing validation protocols and reports, coordinating the execution of validation activities (process, cleaning, equipment, and computer qualifications) across relevant departments. Key Responsibilities: <ul><li>Contribute to the preparation and review of the Validation Master Plan for Process and Cleaning.</li><li>Manage validation requirements for the company and third-party suppliers/CMOs.</li><li>Oversee the preparation, review, and issuance of Validation Protocols and Reports, including equipment, cleaning, process, and computer system validation.</li><li>Maintain and manage the cleaning validation strategy and master plan, ensuring compliance with EU regulations.</li><li>Implement process validation for new products to meet regulatory submission requirements.</li><li>Coordinate execution of validation protocols with Production, Quality Control, and R&D teams.</li><li>Establish and direct validation and revalidation activities.</li><li>Liaise with contract manufacturing customers for protocol and report approvals as needed.</li><li>Review and manage Change Control Forms and Non-Conformances related to validation.</li><li>Update quality documentation related to validation activities.</li><li>Identify and address training requirements for validation support.</li><li>Ensure completion of validation protocols.</li><li>Conduct internal audits and assist in regulatory and customer audits.</li><li>Lead cross-functional teams in resolving technical issues.</li><li>Execute risk assessments and investigation reports related to validation.</li></ul>Competencies: <ul><li>Strong verbal and written communication skills.</li><li>Ability to work independently in an analytical environment.</li><li>Proficient in Word, Excel, and statistical software.</li><li>Knowledge of process and cleaning validation.</li><li>Experience in conducting internal and external audits.</li></ul>Qualifications: <ul><li>B.Sc. or higher in Science or Engineering.</li><li>Minimum 2 years of relevant experience.</li><li>HPRA/USFDA experience preferred.</li><li>Proven ability to work and communicate effectively across all levels.</li></ul>Health & Safety: <ul><li>Follow health and safety protocols, including PPE use in laboratory and production areas.</li><li>Report any safety concerns or defects promptly.</li><li>Maintain a safe, clean, and tidy work environment.</li><li>Required training: Manual Handling and PC operation.</li></ul>Work Environment: <ul><li>Office-based role.</li></ul> By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Niall Finnerty on +353 86 1980270.

Construction Safety Specialist (18 month Fixed Term Contract) Galway Hourly Rate   Responsibilities: <ul><li>Drive the implementation of initiatives to foster a strong construction safety culture.</li><li>Monitor and ensure fulfilment of client’s legal obligations are met at all stages of construction.</li><li>Work with Main Contractor and Sub-Contractor teams to drive overall Construction EHS program implementation.</li><li>Identifying and mitigating environmental and safety risks at construction sites, as well as the transition from design to construction to operational activities.</li><li>Review the ongoing programs, identify areas for improvements and work towards continual improvements.</li><li>Undertake documentation review (including construction H&S plans, traffic management plans, risk assessments and permits)</li><li>Provide regular on-site project presence.</li><li>Undertake Health and Safety compliance evaluations, inspections, and audits at prescribed intervals.</li><li>Develop and deliver safety training as required.</li><li>Monitor EHS performance and intervene/improve where needed.</li><li>Investigate accidents, incidents and near miss events</li><li>Attend weekly, monthly, and quarterly project reviews related to construction safety.</li></ul>Skills: <ul><li>Bachelor’s degree or equivalent qualification related to Construction Health and Safety.</li><li>Qualified to NEBOSH Diploma level or equivalent.</li><li>Experience in managing construction safety across large multi-site businesses.</li><li>Effectively engage and influence other functional leaders and their teams, to build buy-in to EHS strategies and change processes.</li><li>Experienced in operating throughout all stages of the construction lifecycle.</li><li>Proficient in the implementation of Safety Management Systems and safety reporting.</li><li>Project management qualification / skills.</li><li>Strong communication skills.</li></ul>By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes. For more information and a confidential chat please contact Gerard Cunniffe on +353 86 190 8885.

Construction Safety Specialist

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<h1>Meet The Team</h1>

<h3>Our Leadership Team</h3>

<h2>With over 100+ years experience suppoting Engineering Projects &amp; Resources in Europe.</h2>

<h1>About us</h1>

SKIP THE JOB SEARCH

<h5>INVESTED IN YOUR SUCCESS.</h5><h5>What we do is more than a job.</h5>At Sterling, we work every day to create solutions to our clients&rsquo; business challenges while advancing our employees&rsquo; career objectives. We support your team in everything we do, from cutting-edge process development to hiring for your next success. Sterling drives expected outcomes while ensuring safety and compliance within your most complex projects.

Engineering Services

Professional Services

<h5>WHAT WE BUILD ON</h5><h5>At Sterling, we are driven by our values.</h5>For more than five decades, our commitment to quality has been the cornerstone of our success. We always act with integrity&mdash;taking responsibility for our work, caring for our people, and staying focused on safety and sustainability. Respect for people is at the heart of our business&mdash;clients and employees alike. We have an unrelenting focus on inclusion - we are a diverse, well-rounded team of thinkers and doers that embrace all perspectives. This culminates in a positive impact on the work we do.

WHAT WE BUILD ON<h2>At Sterling, we are driven by our values.</h2>For more than five decades, our commitment to quality has been the cornerstone of our success. We always act with integrity&mdash;taking responsibility for our work, caring for our people, and staying focused on safety and sustainability. Respect for people is at the heart of our business&mdash;clients and employees alike. We have an unrelenting focus on inclusion - we are a diverse, well-rounded team of thinkers and doers that embrace all perspectives. A diverse, well-rounded team of thinkers and doers helps Sterling embrace all perspectives. This culminates in a positive impact on the work we do.

<h5 style="text-align: center;">Since 1969, Sterling has been focused on cultivating relationships and&nbsp;is in the business of building trust.</h5>

INVESTED IN YOUR SUCCESS<h2>What we do is more than a job.</h2>At Sterling, we work every day to create solutions to our clients&rsquo; business challenges while advancing our employees&rsquo; career objectives. We support your team in everything we do, from cutting-edge process development to hiring for your next success. Sterling drives expected outcomes while ensuring safety and compliance within your most complex projects.

<h1>Certifications</h1>

<h1>Certifications &amp; Awards</h1>

<h2>PROUD TO BE WOMAN-OWNED.</h2><div class="flex-shrink-0 flex flex-col relative items-end"><div><div class="pt-0"><div class="gizmo-bot-avatar flex h-8 w-8 items-center justify-center overflow-hidden rounded-full"><div class="relative p-1 rounded-sm flex items-center justify-center bg-token-main-surface-primary text-token-text-primary h-8 w-8">&nbsp;</div></div></div></div></div><div class="group/conversation-turn relative flex w-full min-w-0 flex-col agent-turn"><div class="flex-col gap-1 md:gap-3"><div class="flex max-w-full flex-col flex-grow"><div class="min-h-8 text-message flex w-full flex-col items-end gap-2 whitespace-normal break-words [.text-message+&amp;]:mt-5" dir="auto" data-message-author-role="assistant" data-message-id="497c14f8-4331-4cd4-a0a0-847f5c2bf610" data-message-model-slug="gpt-4o"><div class="flex w-full flex-col gap-1 empty:hidden first:pt-[3px]"><div class="markdown prose w-full break-words dark:prose-invert light">We're excited to announce that Sterling Engineering Limited has officially met the qualifications to be named a Certified Women&rsquo;s Business Enterprise by WeConnect International!This certification reflects our commitment to diversity, leadership, and excellence, reinforcing our dedication to empowering women in business.&nbsp;We&rsquo;re proud to continue building strong partnerships and delivering top-quality engineering and staffing solutions with this recognition.<img src="https://cdn.sourceflow.co.uk/yi17tb2pmbvmyho8k83htie7aurb" alt="" width="400" height="179">&nbsp;</div></div></div></div></div></div>

labor were much more favorable

<h1>Careers</h1>

Options for a Fulfilling Career

<h3>NEED HELP WITH YOUR&nbsp;</h3><h3>JOB SEARCH?</h3>

Careers

<h1>Case Studies</h1>

<h1>Clients</h1>

<h2>Engineering Services</h2><h5>Take your projects from planning to reality.</h5>Every project has a range of challenges that need to be met. If your organisation seeks expertise to identify and implement these solutions, you&rsquo;re looking for Sterling Engineering. With decades of experience and a wide range of knowledge, we analyse problems and design solutions.

<h2>Professional Services</h2>Take your projects from planning to reality.Every project has a range of challenges that need to be met. If your organization seeks expertise to identify and implement these solutions, you&rsquo;re looking for Sterling Engineering. With decades of experience and a wide range of knowledge, we analyze problems and design solutions.

<h2>Professional Services</h2><h6>Take your projects from planning to reality.</h6>Every project has a range of challenges that need to be met. If your organization seeks expertise to identify and implement these solutions, you&rsquo;re looking for Sterling Engineering. With decades of experience and a wide range of knowledge, we analyze problems and design solutions.

<h2>Engineering Services</h2><h6>Take your projects from planning to reality.</h6>Every project has a range of challenges that need to be met. If your organization seeks expertise to identify and implement these solutions, you&rsquo;re looking for Sterling Engineering. With decades of experience and a wide range of knowledge, we analyze problems and design solutions.

<h2>Engineering Services</h2>

<h1 style="text-align: center;">CONTACT US</h1>

Knowledge Hub

Our approach to project planning is characterised by:

<h5>Our process is engineered for your success.</h5>

<h3>Why Choose Sterling?</h3>

<h1>Engineering Services</h1>

<h3 style="text-align: center;">Outsourcing engineering project&nbsp;services enable companies to save time,&nbsp;money, and resources.</h3>

<h2 style="text-align: center;">PROJECT LIFE CYCLE</h2>End-to-end project delivery or a la carte services support all engineering and manufacturing stages.

<h3>Our process is engineered for your success.</h3>

<h2>Why Choose Sterling?</h2>

<h2>Outsourcing engineering project services enable companies to save time, money, and resources.</h2>

<h1>Life Science</h1>

<h1>Manufacturing</h1>

<h1>Equipment Engineering</h1>Let&rsquo;s engineer a solution together.

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<h1>Delivering Engineering Projects and Resources since 1969</h1>

Every project has a range of challenges that need to be met. If your organization seeks expertise to identify and implement these solutions, you&rsquo;re looking for Sterling Engineering. With decades of experience and a wide range of knowledge, we analyze problems and design solutions.

<h2>Professional Services</h2>&nbsp;<h6>Take your projects from planning to reality.</h6>Every project has a range of challenges that need to be met. If your organization seeks expertise to identify and implement these solutions, you&rsquo;re looking for Sterling Engineering. With decades of experience and a wide range of knowledge, we analyze problems and design solutions.

<h2>Delivering Engineering Projects and Resources since 1969</h2>

<h1>Industries We Serve</h1>

Connect with a recruiter

Find Your Career With Sterling

<h1>Industry</h1>

YOUR ENGINEERING SERVICES PARTNER

PROFESSIONAL SERVICES YOU CAN TRUST

Industries We Serve

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Send us CV

Kita Gandhi

<h1>Dolores Connolly</h1>

<h1>Our Solutions</h1>

<h3>Professional Services for Engineering providing Temporary, Contract and Permanent Solutions.</h3>Don&rsquo;t see what you&rsquo;re looking for? Ask us about any skill or discipline.&nbsp;

<h4>THE STERLING ADVANTAGE.</h4><ul><li>Dedicated Delivery Teams:<ul><li>Project Manager</li><li>Coordinator</li><li>Researchers</li><li>Recruiters</li><li>Onsite Coordinator (as needed)</li></ul></li><li style="font-weight: bold;">Coordinate and manage secondary suppliers</li><li style="font-weight: bold;">Highly competitive pricing with centralised invoicing</li><li style="font-weight: bold;">Quality compliance and access to top talent</li><li style="font-weight: bold;">Tracking and analytics</li><li style="font-weight: bold;">Monthly/quarterly status reports</li><li style="font-weight: bold;">Flexible benefit programs</li><li style="font-weight: bold;">Technical expertise to deliver a statement of work</li></ul>

At Sterling, we pride ourselves on our exceptional recruitment process. We build strong partnerships with our clients, providing high-touch communication and in-depth prescreening to ensure the perfect match. Our advanced technology and extensive candidate database allow us to effortlessly locate technical candidates that may be difficult to find through other recruiting means. In addition, our dedicated industry-focused talent teams are profoundly knowledgeable and assess technical skills, cultural fit, and alignment with our client&rsquo;s values. We also provide comprehensive onboarding support for a seamless transition and long-term success. As a result, we deliver top-notch talent that aligns perfectly with our client&rsquo;s goals and culture.

<h3>Empowering Success</h3><h3>Together: Our Collaborative</h3><h3>Journey</h3>

<h5>Empowering Success Together: Our Collaborative Journey</h5>

<h3 style="text-align: center;">Professional Service Offering</h3>As a Managed Service Provider (MSP), we specialise in managing and overseeing the staffing process for our clients. Our primary focus is to partner with you to help you efficiently acquire and manage your contingent workforce.&nbsp;

<h4>THE STERLING ADVANTAGE.</h4><ul><li>Dedicated Delivery Teams:<ul><li>Project Manager Coordinator Researchers Recruiters Onsite Coordinator (as needed)</li></ul></li><li>Coordinate and manage secondary suppliers</li><li>Highly competitive pricing with centralized invoicing</li><li>Quality compliance and access to top talent</li><li>Tracking and analytics</li><li>Monthly/quarterly status reports</li><li>Flexible benefit programs</li><li>Technical expertise to deliver a statement of work</li></ul>&nbsp;&nbsp;

<h2>Empowering Success Together: Our Collaborative Journey</h2>

<h2 style="text-align: center;">Professional Service Offering</h2>

<h1>Partnering with us</h1>

<h5>ENGINEERING SERVICES</h5>Sterling&rsquo;s experienced engineers can guide you from concept to prototype production or testing to manufacturing. With experience in multiple industries, we can deliver a creative approach to the project, accelerating time to market.Our experienced, multi-disciplined team of Project Managers, Engineers and Designers, led by licensed Professional Engineers (PE), provide Project Management, Engineering, Design, Commissioning, Qualification, and Validation (CQV) to Manufacturing, OEM, and R&amp;D customers.&nbsp;<h5>PROFESSIONAL SERVICES</h5>Our recruiters are experts in their related industries and talent skill sets. We leverage our industry relationships built since 1969, propriety database, and invested resources to connect you with the best engineering and technical talent.<ul><li>Recruiting structure driven by industry disciplines</li><li>We fully prescreen &amp; qualify candidates before submittal</li><li>90%+ of our business is from repeat clients</li></ul>

<h3>Why Sterling?</h3>

KEY DIFFERENTIATORS

<h2>Why Sterling?</h2>

Our recruiters are experts in their related industries and talent skill sets. We leverage our industry relationships built since 1969, propriety database, and invested resources to connect you with the best engineering and technical talent.&nbsp;<ul><li style="font-weight: bold;">Recruiting structure driven by industry disciplines</li><li style="font-weight: bold;">We fully prescreen &amp; qualify candidates before submittal</li><li style="font-weight: bold;">90%+ of our business is from repeat clients</li><li style="font-weight: bold;">2022 Manage HR Top Contingent Workforce Services Company</li><li>Best of Staffing Awards <ul><li>Client Satisfaction &ndash; 11 Consecutive Years  Talent Satisfaction &ndash; 10 Consecutive Years  Employee Satisfaction &ndash; 4 Consecutive Years</li></ul></li></ul>

KEY DIFFERENTIATORS

<h1>Pillar page</h1>

<h1>Equipment Engineering</h1>

<h2>Service Summary</h2>Elevate your product development journey with our cutting-edge Product Engineering services. We specialize in guiding your product through every stage of development. Our focus on scalability and future-proofing anticipates growth and technological advancements, providing a solid foundation for sustained success. Choose our Product Engineering services for a strategic partnership that goes beyond development &ndash; it&rsquo;s about shaping the future of your product portfolio with innovation, efficiency, and quality at its core.<table style="border-collapse: collapse; width: 100.17%; height: 35px;" border="1"><colgroup><col style="width: 49.8305%;"><col style="width: 49.8305%;"></colgroup><tbody><tr style="height: 17.5px;"><td style="height: 17.5px;">Concepting</td><td style="height: 17.5px;">Detailing</td></tr><tr style="height: 17.5px;"><td style="height: 17.5px;">Product development</td><td style="height: 17.5px;">Reverse engineering</td></tr><tr><td>Simulation</td><td>Materials selection</td></tr><tr><td>Design for manufacturability</td><td>Prototyping</td></tr><tr><td>&nbsp;</td><td>&nbsp;</td></tr></tbody></table>

<h1>Process Engineering</h1>Let&rsquo;s engineer a solution together.&nbsp;

<h1>Product Engineering</h1>Let&rsquo;s engineer a solution together.&nbsp;

<h1>Life Sciences Staffing Solutions</h1>

<h3>Did you know Sterling also provides outsourced design and engineering solutions for the life science industry?</h3>Sterling Engineering has decades of experience working on complex, highly technical projects across various life science clients. We have streamlined our processes, best practices, and customization of manufacturing systems to meet your needs &ndash; saving you time and money.

<h1>Professional Services</h1>

Organisations may encounter various obstacles when searching for technical and engineering talent, such as:

<h3>Professional Services for Engineering providing</h3><h3>Temporary, Contract and Permanent Solutions.</h3>Don&rsquo;t see what you&rsquo;re looking for? Ask us about any skill or discipline.&nbsp;

At Sterling, we pride ourselves on our exceptional recruitment process. We build strong partnerships with our clients, providing high-touch communication and in-depth prescreening to ensure the perfect match. Our advanced technology and extensive candidate database allow us to effortlessly locate technical candidates that may be difficult to find through other recruiting means. In addition, our dedicated industry-focused talent teams are profoundly knowledgeable and assess technical skills, cultural fit, and alignment with our client&rsquo;s values. We also provide comprehensive onboarding support for a seamless transition and long-term success. As a result, we deliver top-notch talent that aligns perfectly with our client&rsquo;s goals and culture.

<h3>Industry Leading Staffing &amp; Recruiting</h3>

<h1>Project Management</h1>Let’s engineer a solution together.

<h1>Start-Up &amp; Documentation</h1>Let&rsquo;s engineer a solution together.&nbsp;

<h1>Strategy</h1>Let&rsquo;s engineer a solution together.&nbsp;

<h1>Transportation</h1>

<h2>JOIN OUR INTERNAL TEAM</h2>

<h1>Join Our Internal Team</h1>

<h2>Find Your Career With Sterling</h2>Sterling is fortunate to have a diverse and exceptional team of individuals with deep experience and expertise. We welcome professionals looking for new challenges, those starting their career journey, and those eager to seize new opportunities in their professional lives. With Sterling, you&rsquo;ll receive:<ul><li>Full benefits</li><li>Employment opportunities that give you flexibility and new challenges</li><li>Consistent opportunities that provide stability</li><li>Expert recruiters that advocate your unique skills</li></ul>

About Karl
With 19 years in recruitment, Karl is a seasoned professional known for connecting unique talents with the right roles.&nbsp;
His experience spans various regions including Europe, San Francisco, Dublin, and London - where he has recruited for global companies, established talent strategies, and specialised in sectors from hospitality to investment banking and now IT and Engineering.&nbsp;
Key to his success is his ability to actively listen, an approach that helps him understand clients' and candidates' needs. Passionate about tech advancements, he has built a vast network in IT and Engineering, maintaining respected relationships that drive his continued success in placing top talent in dynamic, evolving fields.
Outside of work, Karl is known for being heavily involved with various charities raising much needed funds for the local area and wild camping in beautiful Connemara or other parts of the coast of Ireland.

Karl Lippett

Gerard Cunniffe

Eamon Judge

Owen Clancy

Niall Finnerty

Tommy McKeown

About Gerard
With Sterling&rsquo;s expansion into Ireland &amp; Europe, Gerard joined the Sterling Engineering team in 2023. Gerard is a recruitment professional with over a decade of international experience in the Engineering and Construction sectors. Currently serving as the Recruitment Team Lead at Sterling Engineering , Gerard has been instrumental in driving talent acquisition strategies that align with the company&rsquo;s mission to provide exceptional project support and staffing solutions across various industries, including Life Sciences, Automation &amp; Robotics, Manufacturing, Tech, Food &amp; Beverage, and Construction.
His previous experience includes significant positions at 3D Personnel Ltd, LJB Recruit and Aspect Personnel. Gerard specialised in recruiting for key roles in the construction industry across Ireland, UK, Europe and Melbourne.&nbsp;
Gerard's known for building strong relationships with clients and candidates alike and is passionate about connecting top talent with leading organisations.
Outside of work, Gerard can be found at his local GAA pitch, running the roads or in his garden.
Education:
<ul>
<li>Bachelor of Business (Honours) from Institute of Technology, Sligo</li>
</ul>

Gerard Cunniffe 

About Robert
Robert Noble joined Sterling in 2012 following a 30 year distinguished career in the Pharmaceutical Sector. His role is to expand Sterling&rsquo;s engineering services offering and deepen support services to existing clients already engaged in this sector.
Robert was the former Director of Technology and Design Engineering for Abbott Labs&rsquo; Global Pharmaceutical Operations. He has chaired the Packaging Equipment for Pharmaceuticals (PEP) Industry Group for ten years and served on the Packaging Machinery Manufacturers Institute&rsquo;s (PMMI) Packaging Management Council for seven years. He is a graduate of the University of Illinois and has an MBA from Lake Forest Graduate School of Management.
Membership organisations include:
<ul>
<li>International Society of Pharmaceutical Engineers</li>
</ul>

Robert Noble

About Donal
Donal O'Callaghan is a seasoned engineering professional with over 40 years of diverse experience in manufacturing, operations, engineering design, procurement, and construction. Since April 2023, he has acted as a Technical and Business Consultant with Sterling Engineering Ltd., where he focuses on driving sales and marketing initiatives, providing recruitment assistance, and overseeing the conceptual design of Life Sciences projects.
Prior to his role at Sterling, Donal co-founded Callaghan Engineering in 1990, leading the firm to become one of Ireland's premier multi-discipline consulting engineering companies. Under his leadership, Callaghan Engineering served over 200 clients, with more than 85% of sales derived from repeat business.
Throughout his career, Donal has held key positions in project management, with significant assignments in the biopharma and medical devices sectors. His commitment to engineering excellence and sustainability has driven his ongoing success in the industry. He has also acted as a Senior Inspector with An Bord Pleanala, mainly in the area of air/water pollution appeals.
Project Highlights:
<ul>
<li>Merck, Co. Cork: Project Manager for a &euro;36 million Media Manufacturing Plant and a $75 million membrane manufacturing facility.</li>
<li>Pfizer, Little Island: Oversaw a &euro;4 million Centrifuge Project and a &euro;1.5 million Front End Study.</li>
<li>Abbott Diagnostics, Longford: Directed a &euro;13.5 million facility upgrade in diagnostics.</li>
<li>Data Centre Facility, Dublin: Managed a &euro;55 million investment for a confidential client.</li>
<li>Amgen, Co. Dublin: Led a &euro;25 million Containment Project.</li>
<li>EU Presidency: Led an engineering team for Ireland&rsquo;s last Presidency of the EU, providing facilities for the print and broadcast media</li>
</ul>
Education &amp; Qualifications:
<ul>
<li>B.E. in Chemical Engineering, University College Dublin</li>
<li>Diploma in Project Management, University of Dublin</li>
<li>Member of The Institute of Directors (M.Inst.D)</li>
<li>Member of the International Society of Pharmaceutical Engineering (M.ISPE)</li>
<li>Chartered Engineer (CEng)</li>
<li>Fellow of Engineers Ireland (F.I.E.I)</li>
<li>Fellow of the Institution of Chemical Engineers (FIChemE)&nbsp;</li>
</ul>

Donal O'Callaghan

About Kita
Kita joined Sterling in 2021 as our Director of Life Sciences Engineering.
Kita has more than 20 years of engineering and management experience, including 16 years in engineering roles with Abbott Laboratories and AbbVie, a global research-driven biopharmaceutical company. Kita works to expand Sterling&rsquo;s engineering services offering and to deepen support services to existing clients already engaged in the pharmaceutical and medical device sectors.
Kita is a PMP-certified chemical engineer, project manager, and entrepreneur with experience in both large corporate and small business environments.&nbsp;
Project Highlights:
<ul style="margin-top: 0in;" type="disc">
<li class="MsoListParagraph" style="margin-left: 0in; mso-list: l0 level1 lfo1;">Implemented Calibration Streamlining Program at pharmaceutical manufacturing sites in Germany, Ireland, and UK.</li>
<li class="MsoListParagraph" style="margin-left: 0in; mso-list: l0 level1 lfo1;">Developed business processes and provided training in conjunction with implementing a new corporate CMMS system at multiple European manufacturing sites.</li>
<li class="MsoListParagraph" style="margin-left: 0in; mso-list: l0 level1 lfo1;">Evaluated site infrastructure and generated site master plan, five-year long-range plan, and expansion conceptual design for Netherlands pharmaceutical warehouse.</li>
</ul>
Education &amp; Qualifications:
<ul>
<li>Bachelor of Science degree in Chemical Engineering from Washington University in St. Louis</li>
<li>Master of Science degree in Chemical Engineering from the University of California, Berkeley.</li>
</ul>

About Tim
Tim Silkaitis joined Sterling Engineering in 1992 as an Accounting Clerk. In 1997, he was promoted to an Accounting Manager and then in 2006 to Controller. As VP of Finance, he oversees all financial matters &mdash; including P &amp; L, 401(k), payroll services, and health insurance.
Tim is responsible for legal and contract administration and has IT department oversight.
Education:&nbsp;
<ul>
<li>Bachelors of Science Degree from Elmhurst College</li>
<li>MBA from DePaul University.</li>
</ul>

Tim Silkaitis

About Mark
Mr. Howard has extensive experience owning and operating two successful start-ups through sale. One acquirer was Waterlogic Plc, a publicly traded company on the AIM Exchange in London. Post acquisition he stayed on as Vice President of Sales and was part of the mergers and acquisitions team. 
Since joining Sterling Engineering in 2012 he has been a valuable contributor with progressive leadership roles primarily focused on our Life Science business vertical as well as in Sales and Operational leadership across the Technology, Health/Wellness, Facility, Manufacturing, and Engineering sectors.&nbsp; 
Mr. Howard was part of the tactical team sent to evaluate expanding Sterling Engineering&rsquo;s operations to Europe in 2019. As Senior Executive Vice President, Mr. Howard oversees operations for the Engineering Services Company and our European entity officed in Ireland.
Positions held: Sales Representative, Business Development Manager, Branch Sales Manager, Regional Manager, National Vice President of Sales, President/CEO.
Mark is proud to be a member of the&nbsp;<a href="https://diversityallianceforscience.com/">Diversity Alliance for Science</a>.

Mark Howard

About Dolores
Dolores Connolly has served as CEO of Sterling Engineering since 1997.&nbsp;
Prior to that, she worked with Danka Corporation, a global technology company, as Regional VP for Sales/Service. With 450+ employees supporting the project needs of Fortune 500 and mid-sized companies in the pharmaceutical, food, transportation, logistics, and packaging industries, Sterling is a recognized market leader both nationally and globally. Ms. Connolly&rsquo;s civic engagement is focused primarily on STEM education initiatives and efforts focused on breaking the cycle of poverty, particularly related to women and girls locally and globally. Dolores is proudly involved with the following organisations:
<ul>
<li>TechServe Alliance &ndash; an organization dedicated to supporting Engineering/IT businesses</li>
<li>Chicago Council Immigration Task Force</li>
<li>Chicago Council on Global Affairs</li>
<li>Presidents Circle</li>
<li>International Women&rsquo;s Forum</li>
<li>WMBE Chicago</li>
<li>Executive Board Member of Concern Worldwide, an international humanitarian organization working in 26 of the poorest countries as ranked by World Bank Index</li>
</ul>

Quality Control Analyst

Owen Clancy

Moulding Process Engineer

IT Systems Engineer

Plant Electrician

Sterilisation Engineer

Quality Control Analyst

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