Job Title:     Health & Safety Officer Location:     Limerick Status:      Permanent Position Summary: <ul><li>My client based in South Limerick are seeking an established Health & Safety Officer to join a dynamic team.</li><li>You will be the face of Health & Safety in the plant collaborating with employees on a daily basis.</li></ul>  Key Responsibilities: <ul><li>Provide specialist advice, guidance and instruction regarding Health & Safety to employees ensuring that high standards in Health and Safety are maintained.</li><li>Facilitate Compliance and Implementation of Health and Safety procedures.</li><li>Promote a positive Health and Safety Culture.</li><li>Provide effective and efficient support to Senior Management and colleagues to ensure safe systems of work and practice are maintained.</li><li>Review existing policies and measures and update according to legislation.</li><li>Schedule Monthly Safety Audits/Inspections for every department within the company.</li><li>Maintain accurate records relating to Health and Safety documentation.</li></ul>  Qualifications and Requirements: <ul><li>Experience in health and safety procedures and qualification is essential.</li><li>Hazard/incident investigation and strong analytical / problem solving skills.</li><li>Have a keen interest in Health and Safety, Welfare.</li><li>Strong analytical and problem solving skills</li></ul>  For a confidential conversation about the position 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

Health & Safety Officer

We are currently seeking an experienced Quality Manager to join a leading medical device manufacturing organisation. This is an excellent opportunity for a quality professional with strong leadership experience and a proven track record in quality systems, regulatory compliance, and continuous improvement within a regulated manufacturing environment. The successful candidate will be responsible for overseeing all aspects of the Quality Management System (QMS), ensuring compliance with industry standards and regulatory requirements while leading quality initiatives across the business. Key Responsibilities:  Quality Management Systems & Compliance <ul><li>Act as Management Representative for the Quality Management System (QMS).</li><li>Ensure QMS processes and documentation are established, implemented, maintained, and continuously improved.</li><li>Maintain compliance with ISO 13485, ISO 9001, FDA 21 CFR Part 820, and other applicable regulatory requirements.</li><li>Monitor QMS performance and identify opportunities for improvement.</li><li>Promote quality and regulatory awareness throughout the organisation.</li><li>Lead Management Review activities and ensure compliance with regulatory expectations.</li><li>Oversee document control and quality records management.</li></ul> Audits & Regulatory Affairs <ul><li>Serve as the primary point of contact for external audits conducted by customers, certification bodies, and regulatory authorities.</li><li>Plan, manage, and conduct internal quality audits.</li><li>Ensure effective implementation of corrective actions arising from audit findings.</li></ul> Quality Operations <ul><li>Lead and oversee CAPA, non-conformance management, customer complaints, and quality investigations.</li><li>Ensure timely resolution of quality issues and implementation of effective corrective and preventive actions.</li><li>Support product development, manufacturing, and product release activities.</li><li>Ensure Quality Control operations are effective and aligned with quality objectives.</li><li>Authorise product disposition decisions and escalate quality concerns where necessary.</li><li>Take appropriate action, including stopping production or shipment, to prevent non-conforming products reaching customers.</li></ul> Supplier Quality Management <ul><li>Review, approve, and monitor suppliers of materials, components, products, and services.</li><li>Support supplier qualification, audits, and performance management activities.</li><li>Ensure supplier compliance with quality requirements and standards.</li></ul> Requirements Education & Experience <ul><li>5–10 years' experience in Quality Assurance and/or Quality Control within medical device manufacturing or a similarly regulated industry.</li><li>Demonstrated experience managing quality systems and regulatory compliance programs.</li><li>Previous people management and leadership experience.</li></ul> Technical Knowledge <ul><li>ISO 13485</li><li>ISO 9001</li><li>FDA 21 CFR Part 820</li><li>Medical Device regulations and quality standards</li><li>FMEA</li><li>DOE</li><li>SPC</li><li>Statistical analysis techniques</li><li>Experience managing audits, CAPA systems, supplier quality, and complaint handling processes.</li></ul>Skills & Competencies <ul><li>Strong leadership and decision-making abilities.</li><li>Excellent problem-solving and analytical skills.</li><li>Outstanding written and verbal communication skills.</li><li>Ability to influence and collaborate effectively across all levels of an organisation.</li><li>Strong organisational and project management capabilities.</li><li>Willingness to travel as required for supplier visits, audits, and business needs.</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Quality Manager

As a Senior Quality Assurance Engineer, you will play a key role in ensuring product quality, regulatory compliance, and effective quality system implementation across both production and New Product Development (NPD) / New Product Introduction (NPI) activities. You will work closely with cross-functional teams to support quality processes, drive continuous improvement initiatives, and ensure products and processes meet customer, regulatory, and internal requirements Key Responsibilities: <ul><li>Provide Quality Assurance support across manufacturing and NPD/NPI activities, ensuring compliance with Quality Management System (QMS) requirements and applicable regulatory standards.</li><li>Support client programmes involving the development and implementation of new products, materials, and processes, including associated quality documentation.</li><li>Review and approve quality documentation to support pilot builds, scale-up activities and successful transfer to production.</li><li>Conduct and support risk management activities, including DFMEA and PFMEA, ensuring effective identification and mitigation of quality risks.</li><li>Manage and support core quality processes including CAPA, non-conformance management, change control and product release activities.</li><li>Partner with cross-functional teams to investigate quality issues, identify root causes and implement effective corrective and preventive actions.</li><li>Support internal, customer, and supplier audits, including the management and closure of audit findings.</li><li>Review and approve procedures, work instructions, and quality records to ensure compliance and accuracy.</li><li>Interface with customers and suppliers on quality-related matters, maintaining strong professional relationships.</li><li>Support supplier quality activities, including supplier qualification and performance monitoring.</li><li>Ensure documentation is maintained in accordance with QMS and regulatory requirements across both development and commercial operations.</li><li>Contribute to continuous improvement initiatives aimed at enhancing product quality, compliance, and operational effectiveness.</li><li>Support site audit readiness activities and regulatory inspections as required.</li></ul> Requirements: <ul><li>Bachelor’s Degree in Engineering or a related technical discipline.</li><li>Minimum 10 years’ Quality Assurance experience within the medical device industry.</li><li>Proven experience supporting New Product Development (NPD) and New Product Introduction (NPI) activities.</li><li>Strong working knowledge of ISO 13485, FDA QSR, and medical device quality system requirements.</li><li>Demonstrated experience with CAPA, non-conformance management, change control, and quality investigations.</li><li>Experience supporting internal, customer, supplier, and regulatory audits.</li><li>Strong understanding of risk management principles, including DFMEA and PFMEA.</li><li>Experience working within both development and manufacturing environments.</li><li>Familiarity with electronic Quality Management Systems (eQMS) is advantageous.</li><li>Excellent communication and stakeholder management skills.</li><li>Strong organisational skills with the ability to work independently and manage multiple priorities.</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Senior Quality Assurance Engineer

Job Title:    Process Development Engineer    Location:    Galway Status:      Permanent Position Summary: <ul><li>The Process Development Engineer will provide hands-on engineering support to the machine assembly team, with a strong focus on enhancing manufacturing processes, improving efficiency, and reducing costs.</li><li>The ideal candidate will have experience in a manufacturing environment, with a demonstrated ability to identify process inefficiencies, implement effective improvements, and deliver measurable cost-saving and productivity-enhancing initiatives.</li></ul>  Key Responsibilities: <ul><li>Provide engineering support to the machine assembly team, troubleshooting production issues and implementing timely solutions to maintain production flow</li><li>Manage documentation, presentations, and records for engineering projects</li><li>Support machine build and assembly activities, including troubleshooting and optimization</li><li>Identify and implement process improvements across assembly and manufacturing operations</li></ul>  Qualifications and Requirements: <ul><li>Experience in a manufacturing or engineering environment</li><li>Experience in machine building, equipment assembly, or production line development</li><li>Experience with ERP systems & CAD tools</li><li>Minimum level 7 Bachelor’s Degree in an Engineering discipline</li></ul>  For a confidential conversation about the position 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

Process Development Engineer

Validation Engineer We are seeking an experienced Validation Engineer to join our Quality Assurance and Validation team. The successful candidate will play a key role in the validation and qualification of equipment, utilities, processes, and software systems in compliance with cGMP, FDA, European GMP, and GAMP standards. This position requires strong technical expertise in aseptic processing validation, autoclave validation, HVAC systems, and clean utility validation within a pharmaceutical or biotechnology manufacturing environment. Key Responsibilities <ul><li>Participate actively in the site Validation Program and broader Quality Assurance activities.</li><li>Coordinate, direct, and execute validation and qualification activities for equipment, utilities, processes, and software systems.</li><li>Generate, maintain, and execute Validation Plans, protocols, schedules, and final reports in accordance with cGMP requirements.</li><li>Support validation investigations, deviation management, and implementation of corrective and preventive actions (CAPAs).</li><li>Supervise vendors and contractors performing validation activities on site.</li><li>Execute and support qualification and requalification activities for:<ul><li>Autoclaves</li><li>Parts Washers</li><li>Lyophilizers (Lyo)</li><li>CIP/SIP Systems</li><li>VHP Systems</li><li>Temperature Mapping Studies</li></ul></li><li>Perform aseptic processing validation activities including media fills and VHP validation execution.</li><li>Support HVAC validation activities and environmental qualification programs.</li><li>Create, review, and approve validation and qualification documentation.</li><li>Manage validation-related change controls, exception events, and documentation processes.</li><li>Ensure all validation activities are documented in compliance with cGMP and company procedures.</li><li>Deliver cross-training within the validation team and support onboarding/training of new team members.</li><li>Participate in continuous improvement initiatives relating to manufacturing, quality, safety, and training systems.</li><li>Coordinate team activities to maximize efficiency and compliance.</li><li>Communicate effectively with peers, cross-functional teams, and management regarding validation activities, issues, and escalation of concerns where necessary.</li></ul> Requirements <ul><li>Bachelor’s degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related discipline.</li><li>Minimum 5 years’ experience in validation within a pharmaceutical, biotechnology, or regulated manufacturing environment.</li><li>Proven experience in:<ul><li>Autoclave validation execution</li><li>Aseptic processing validation</li><li>Media fill execution</li><li>VHP validation</li><li>HVAC validation</li></ul></li><li>Strong understanding of:<ul><li>FDA and European cGMP regulations</li><li>GAMP guidelines</li><li>Validation lifecycle principles</li><li>Change control and deviation management</li></ul></li><li>Experience generating and executing validation protocols and reports.</li><li>Excellent documentation, communication, and organizational skills.</li><li>Ability to work independently and collaboratively within cross-functional teams</li></ul> Desirable Experience <ul><li>Experience with sterile manufacturing environments.</li><li>Knowledge of cleanroom qualification and environmental monitoring systems.</li><li>Experience supporting audits and regulatory inspections.</li><li>Familiarity with computerized system validation (CSV) and data integrity principles</li></ul>For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Validation Engineer

Job Title:    Cyber Security Engineer Location:    Shannon Status:      Permanent Position Summary: <ul><li>We are seeking a hands-on IT & Cyber Security Engineer to join my clients IT team within a large multinational where security excellence and operational delivery go hand in hand.</li><li>The successful candidate will own and drive the organisation's security accreditation and certification programme while continuously improving security maturity toward recognised industry standards.</li></ul>  Key Responsibilities: <ul><li>Enhance security maturity aligned with ISO 27001 and recognised industry frameworks</li><li>Secure configuration of servers, endpoints, and cloud services</li><li>Support external assessors during audits, penetration testing, and verification activities</li><li>Prepare and maintain documentation, evidence, and artefacts required for security audits and technical assurance activities</li></ul> Qualifications and Requirements: <ul><li>Hands-on experience in an IT role with cybersecurity as a primary focus Strong experience with Microsoft 365, Azure, Active Directory, and VMware / vCentre</li><li>Familiarity with security audit processes, evidence requirements, and technical testing expectations</li><li>Experience owning and maintaining security policies and procedures</li><li>Cyber security certifications</li></ul>For a confidential conversation about the position 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

Cyber Security Engineer

Information Technology Manager Role Overview: We are partnering with a leading manufacturing organisation to recruit an experienced Information Technology Manager for a key leadership role based in Galway, Ireland. This position will oversee IT operations across European and North American sites, with a strong focus on ownership and leadership of the IFS ERP environment across manufacturing operations. Key Responsibilities: <ul><li>Lead end-to-end IFS ERP implementation projects across multiple sites</li><li>Act as the regional SME for IFS ERP across Manufacturing, Supply Chain, Maintenance, Finance, and HR modules</li><li>Drive ERP optimisation, integrations, upgrades, user support, and governance</li><li>Manage regional IT operations and service delivery across EU and North America</li><li>Support cyber-security, compliance, audit readiness, and IT governance initiatives</li><li>Partner with business leaders and global IT teams to deliver strategic technology improvements</li><li>Lead and develop regional IT teams and third-party service providers</li></ul> Knowledge / Experience: <ul><li>10–15 years’ IT experience with strong hands-on IFS ERP expertise</li><li>Proven experience delivering full lifecycle IFS implementations</li><li>Strong background in manufacturing environments and ERP integration (MES/WMS/LIMS/BI)</li><li>Experience across Azure, Entra ID (AAD), Intune, and Microsoft 365</li><li>Knowledge of cyber-security operations and IT governance</li><li>Excellent stakeholder and vendor management skills</li><li>Experience within regulated industries such as medical devices or pharma is highly desirable</li></ul> Additional Information: <ul><li>Regional scope across EU and North America</li><li>Occasional travel required</li><li>Opportunity to play a strategic role in a growing and evolving technology environment</li></ul>  For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Information Technology Manager

We are currently recruiting for an experienced Aseptic Manufacturing Subject Matter Expert (SME) to join a leading biologics manufacturing operation. This is an exciting opportunity for an engineering professional with strong aseptic manufacturing experience to play a key role in supporting sterility assurance, operational excellence, and continuous improvement across a state-of-the-art manufacturing facility. The successful candidate will act as the technical SME for aseptic manufacturing equipment, cleanroom environments, and utility systems, ensuring systems operate in compliance with GMP, regulatory requirements, and aseptic best practices. Key Responsibilities <ul><li>Act as the Subject Matter Expert for equipment, cleanroom, and utility systems related to aseptic manufacturing</li><li>Ensure systems operate in compliance with safety, environmental, GMP, and aseptic manufacturing standards</li><li>Monitor and support aseptic manufacturing engineering systems, including:</li><li>Cleanroom performance (temperature, humidity, differential pressure, airflow velocity)</li><li>Utility systems</li><li>Critical equipment cycles including CIP, SIP, VHP, autoclaves, lyophilization, depyrogenation, and aseptic filling operations</li><li>Support troubleshooting and investigations relating to equipment, utilities, and cleanroom systems</li><li>Participate in investigations related to sterility assurance, media fills, environmental monitoring excursions, and contamination control</li><li>Drive root cause analysis and CAPA implementation activities</li><li>Support continuous improvement initiatives within aseptic manufacturing engineering systems and procedures</li><li>Provide technical input into equipment, cleanroom, and utility system design activities</li><li>Ensure engineering changes are managed through site change control procedures</li><li>Lead projects related to aseptic manufacturing systems and equipment improvements</li><li>Support preventative maintenance strategies for critical systems</li><li>Participate in regulatory inspections and audits as the engineering SME for aseptic operations</li><li>Contribute to contamination control strategies and aseptic process improvements</li><li>Promote a strong quality culture, operational excellence, and continuous improvement mindset across the site</li></ul> Requirements <ul><li>Degree qualification in Engineering or a related technical discipline</li><li>Minimum 3 years’ experience within a GMP-regulated manufacturing environment</li><li>At least 1 year of experience supporting aseptic manufacturing operations</li><li>Strong understanding of GMP and aseptic regulatory requirements</li><li>Experience supporting cleanrooms, utilities, and critical process equipment</li><li>Project management experience is highly desirable</li><li>Excellent communication and stakeholder management skills</li><li>Strong problem-solving, investigation, and risk assessment capabilities</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Aseptic Operations Engineer

Overview We are seeking a motivated and ambitious Business Development Executive to join our clients growing team. based in Dundalk, this role offers hands-on experience across multiple business functions and is an excellent opportunity for a student or recent graduate looking to gain real-world experience in a fast-paced environment. Key Duties & Responsibilities <ul><li>Identify key customers and build strong relationships to generate new sales opportunities and support year-on-year sales growth.</li><li>Develop and implement marketing plans to reach target audiences through social media, conferences, exhibitions, and other channels.</li><li>Engage proactively with customers to generate leads, track projects, promote new business lines, and drive sales performance.</li><li>Champion the needs of new customers and ensure a positive customer experience.</li><li>Manage the new customer sales pipeline and support incremental sales targets.</li><li>Prepare regular reports on sales and business development activities, including progress against key performance indicators (KPIs).</li><li>Gather and provide competitor intelligence to support product costing, market development, and product positioning strategies.</li><li>Provide feedback on issues that may impact customer relationships and business performance.</li><li>Collaborate with internal teams to support the development of innovative products and service offerings.</li><li>Work closely with Marketing and Product Management teams to develop campaigns for new technologies and solutions.</li></ul> Qualifications & Experience <ul><li>Currently studying or recently graduated in Marketing, Business, Communications, or a related field.</li><li>Strong written and verbal communication skills.</li><li>Excellent organisational skills with the ability to multitask and meet deadlines.</li><li>Analytical mindset with an interest in data and reporting; experience with Google Analytics or similar tools is beneficial.</li><li>Proficient in Microsoft Office applications, including Word, Excel, and PowerPoint.</li><li>Experience with CRM or CMS platforms is an advantage.</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Business Development Exec

Engineering Manager Location: Galway, Ireland Employment Type: Permanent / Full-Time Department: Operations Reports To: Operations Director Role Overview The Engineering Manager will lead and develop the engineering team while driving operational performance, continuous improvement, and delivery of engineering objectives aligned with business goals. Key Responsibilities <ul><li>Lead, coach, and develop a high-performing engineering team.</li><li>Manage engineering priorities, resources, and project delivery.</li><li>Drive continuous improvement initiatives focused on efficiency, OEE, and process optimisation.</li><li>Support preventative maintenance and operational excellence activities.</li><li>Partner cross-functionally with Operations, Quality, and other departments.</li><li>Drive effective problem-solving, root cause analysis, and corrective actions through the QMS.</li><li>Monitor KPIs, budgets, and departmental performance.</li><li>Support internal and external audits.</li></ul>Qualifications & Experience <ul><li>Degree in Engineering (preferably Polymer or Mechanical).</li><li>Lean and/or Six Sigma qualification preferred.</li><li>5 years’ experience in a similar engineering leadership role.</li><li>Proven people management and stakeholder engagement experience.</li><li>Strong technical, analytical, and problem-solving skills.</li></ul>Key Competencies <ul><li>Leadership and team development</li><li>Continuous improvement mindset</li><li>Strong communication and collaboration skills</li><li>Project and operational management</li><li>Decision-making and problem-solving capability</li></ul>Working Environment <ul><li>Standard office and manufacturing environment.</li><li>Occasional travel and after-hours support may be required.</li></ul>Benefits <ul><li>Opportunity to work in a growing engineering environment.</li><li>Collaborative and cross-functional culture.</li><li>Professional development and career growth opportunities.</li></ul>

Engineering Manager

Manufacturing Engineering Manager Shannon, Co. Clare Reports to: Chief Operations Officer Overview An exciting opportunity for an experienced Manufacturing Engineering Manager to lead engineering activities across New Product Introduction (NPI), automation, facilities, and high-volume production support within a fast-paced electronics manufacturing environment. The successful candidate will play a key role in driving manufacturing excellence, operational scalability, automation strategy, and technical leadership across the site. Key Responsibilities New Product Introduction (NPI) <ul><li>Lead Manufacturing Engineering support from design phase through to full production ramp-up.</li><li>Drive DFM/DFT activities and develop scalable manufacturing processes.</li><li>Support PFMEA, process validation, control plans, and production handover activities.</li><li>Ensure NPI projects are delivered on time, within budget, and to target yield metrics.</li></ul>Automation & Continuous Improvement <ul><li>Support development and execution of automation strategy across manufacturing and testing operations.</li><li>Identify opportunities to improve productivity, quality, and operational efficiency through automation.</li><li>Drive continuous improvement initiatives across manufacturing operations.</li></ul>Facilities & Production Support <ul><li>Support facilities expansion, layout optimisation, and infrastructure projects.</li><li>Provide technical leadership for complex production issues and manufacturing escalations.</li><li>Work closely with Maintenance, Quality, Supply Chain, and Operations teams to improve manufacturing performance.</li></ul>Leadership <ul><li>Lead and develop a high-performing Manufacturing Engineering team.</li><li>Promote a culture of accountability, collaboration, innovation, and operational excellence.</li></ul>Requirements <ul><li>Bachelor’s Degree in Mechanical, Electronic, Manufacturing, or Industrial Engineering.</li><li>7–10 years’ experience within high-volume electronics manufacturing.</li><li>3–5 years in an engineering leadership role.</li><li>Strong experience in:<ul><li>NPI industrialisation</li><li>Automation projects</li><li>Manufacturing process development</li><li>Production support</li></ul></li><li>Excellent stakeholder management and problem-solving skills.</li><li>Experience managing capital projects and driving continuous improvement initiatives.</li></ul>Key Skills <ul><li>NPI & Process Development</li><li>Automation & Manufacturing Improvement</li><li>PFMEA / Process Validation</li><li>Production Support & Troubleshooting</li><li>Leadership & Team Development</li><li>CapEx & ROI Analysis</li><li>Cross-Functional Collaboration</li><li>Continuous Improvement</li></ul>

Manufacturing Engineering Manager

Job Title:    Financial Controller Location:    Galway Status:      Permanent Position Summary: <ul><li>Seeking an experienced, driven, and highly capable Financial Controller to join my client’s team and support the next phase of their journey. Reporting directly to the senior leadership team, the successful candidate will oversee the company’s day-to-day financial operations.</li><li>This is a hands-on and diverse role that combines managing core financial activities with developing scalable processes and systems to support continued expansion.</li><li>It offers a unique opportunity to play a key role in shaping the growth of a fast-growing international business by helping build the structures, controls, and culture needed for long-term success.</li></ul> Key Responsibilities: <ul><li>Partner with senior leadership to provide financial insight and support strategic decision-making</li><li>Prepare board-level reporting packs and KPI dashboards</li><li>Oversee and manage the financial operations of the group (2 entities), ensuring accuracy, integrity, and timeliness of reporting</li><li>Act as the primary point of contact for outsourced finance contractors, providing direction, review, and quality control</li></ul> Qualifications and Requirements: <ul><li>Experience managing or working with outsourced finance functions or shared service providers</li><li>Strong understanding of financial controls, governance, and best practice process design</li><li>Experience in life sciences, biotech, medtech, or a regulated environment is advantageous</li><li>Qualified accountant (ACA / ACCA / CIMA or equivalent)</li><li>Proven experience in a Financial Controller or senior finance role within a scaling or high-growth environment</li></ul>  For a confidential conversation about the position 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

Financial Controller

Warehouse Assistant Role: Warehouse Assistant Reports to: Operations Manager Location: Galway Role Overview The Warehouse Assistant plays a key role in supporting efficient warehouse operations, including the receipt, storage, and distribution of materials, components, and finished products. The role requires strict adherence to safety standards and regulatory requirements within a controlled environment. Key Responsibilities <ul><li>Shipping Coordination Assist R&D, Operations, and Quality teams in preparing shipments and coordinating with carriers to ensure timely dispatch of materials, components, and products.</li><li>Material Coordination Manage the movement and storage of materials, components, and products within the warehouse and external storage locations.</li><li>Storage Organisation Ensure all materials and products are stored in accordance with company procedures, including correct labelling and segregation.</li><li>Collaboration Work closely with cross-functional teams (R&D, Operations, Quality) to support workflow efficiency and resolve any issues.</li><li>Consumables Management Monitor stock levels of consumables and coordinate ordering to maintain adequate supply.</li><li>Warehouse Maintenance Maintain a clean, organised, and compliant warehouse environment in line with health and safety regulations.</li></ul>    Qualifications & Experience <ul><li>Previous experience in a warehouse or logistics environment (medical or healthcare industry preferred)</li><li>Familiarity with inventory management systems and basic computer skills</li><li>Strong attention to detail and accuracy</li><li>Excellent organisational and time management skills</li><li>Good communication skills and team-oriented approach</li><li>Understanding of warehouse health and safety regulations</li></ul>

Warehouse Assistant

Supply Chain Manager Reports to: VP of Operations Location: On-site Role Overview An experienced and detail-oriented Supply Chain Manager is required to lead end-to-end materials management across the supply chain—from supplier receipt through production to delivery of finished goods. This role ensures material availability, inventory integrity, and supply continuity within a regulated manufacturing environment. Key Responsibilities Inventory & Warehouse Management<ul><li>Maintain optimal inventory levels to support uninterrupted production.</li><li>Oversee receipt, storage, and issuance of materials, ensuring proper labelling, segregation, and storage conditions.</li><li>Manage stock across internal and external locations.</li><li>Monitor reorder points, shelf life, and expiry to prevent shortages or obsolescence.</li><li>Lead annual physical inventory and resolve discrepancies.</li></ul>Planning & Operations<ul><li>Align materials availability with production demand through close collaboration with planning and operations teams.</li><li>Support production scheduling based on demand plans.</li><li>Coordinate with Quality on inspection and release of materials.</li><li>Manage purchase orders in line with supplier agreements.</li><li>Lead ERP system implementation and maintain accurate master data.</li><li>Participate in S&OP processes to ensure balanced production planning.</li><li>Track and deliver key KPIs such as OTIF and supplier performance.</li></ul>Supplier Management<ul><li>Act as primary point of contact for suppliers.</li><li>Manage supplier performance, pricing, and service level agreements.</li><li>Monitor delivery performance and resolve issues.</li><li>Lead supplier forecasting and planning activities.</li><li>Support corrective actions and continuous improvement initiatives.</li><li>Identify and mitigate supply chain risks.</li></ul>People & Stakeholder Management<ul><li>Lead and develop the supply chain team.</li><li>Build strong relationships with internal stakeholders across operations, quality, and commercial functions.</li><li>Collaborate with external partners including suppliers and logistics providers.</li></ul>Experience & Qualifications<ul><li>Degree in Supply Chain, Business, Engineering, Science, or related field.</li><li>Experience in supply chain, materials, or inventory management, including leadership responsibility.</li><li>Background in a regulated manufacturing environment preferred.</li><li>Experience with ERP systems and S&OP processes.</li><li>Knowledge of quality management systems is advantageous.</li></ul>Skills & Competencies<ul><li>Strong analytical and problem-solving skills.</li><li>Excellent organisation and prioritisation ability.</li><li>Continuous improvement mindset.</li><li>Effective cross-functional communication skills.</li><li>High attention to detail, particularly in regulated environments.</li><li>Self-motivated with the ability to work independently.</li></ul>

Supply Chain Manager

Job Title:      Environmental Health & Safety Supervisor Location:      Galway Status:       Permanent Position Summary: <ul><li>This a hands-on EHS Supervisor role with a strong plant floor presence.</li><li>Leads site-level Environmental, Health & Safety (EHS) execution</li><li>Embeds safety and environmental controls into daily operations</li></ul> Key Responsibilities: <ul><li>Lead site-wide execution of Health, Safety & Environmental (EHS) standards, ensuring compliance with ISO 14001/45001, maintaining strong shop-floor presence, and embedding safe practices through coaching and constructive challenge.</li><li>Own the EHS operating rhythm, including daily management systems, action tracking, investigations, and ensuring root causes are addressed with sustainable corrective actions while monitoring and escalating risks.</li><li>Manage EHS training and capability development by maintaining the training matrix, coordinating delivery, tracking compliance, and enabling supervisors and managers to take ownership of safety in their areas.</li><li>Oversee environmental controls and compliance, including chemical management, waste handling, while supporting audits and maintaining accurate documentation.</li></ul>Qualifications and Requirements: <ul><li>Experience in a manufacturing or operational environment</li><li>Strong interpersonal skills, the ability to influence and communicate effectively, and a proactive approach to safety.</li><li>Working knowledge of Environment, Health & Safety legislation and experience supporting environmental management systems.</li><li>Third-level qualification in EHS or related field, or equivalent experience.</li></ul>For a confidential conversation about the position 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

Health & Safety Supervisor

Site Supervisor / Foreman – Industrial Steel & Mechanical Installations We are seeking an experienced Site Supervisor / Foreman to lead and manage industrial installation and maintenance projects within steel fabrication and mechanical engineering environments. This is a hands-on leadership role suited to someone who can confidently run site operations, supervise a mobile crew, and ensure all works are delivered safely, on time, and to a high standard. Key Responsibilities <ul><li>Supervise and actively participate in structural steel installation works, including platforms, stairways, walkways, handrails, and support structures</li><li>Lead industrial installation and maintenance projects, including machinery/equipment fitting and shutdown maintenance</li><li>Manage and coordinate a mobile site crew across multiple client sites</li><li>Interpret technical drawings and specifications to direct site activities</li><li>Plan daily work schedules, allocate tasks, and ensure productivity targets are achieved</li><li>Maintain strong health & safety compliance across all site operations</li><li>Liaise with site management and internal teams to ensure smooth project delivery</li><li>Oversee tools, equipment, materials, and site resources</li></ul> Requirements <ul><li>Proven experience in a supervisory role within steel fabrication, mechanical fitting, or industrial installation environments</li><li>Strong hands-on background in structural steelwork or industrial maintenance</li><li>Competent MIG and stick (arc) welding skills for onsite fabrication and repair</li><li>Ability to read and interpret technical drawings and specifications</li><li>Strong leadership, communication, and organisational skills</li><li>Experience working in live industrial or manufacturing environments (desirable)</li><li>Full clean Irish/EU driving licence</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Site Foreman / Supervisor

Job Title: Fabricator / Welder Location: Leitrim, Ireland (including site-based work) Job Type: Full-Time, Permanent About the Role We are currently recruiting on behalf of a well-established steel fabrication company for an experienced Fabricator/Welder. This is an excellent opportunity to join a growing organisation delivering high-quality fabrication projects across a range of industries. The successful candidate will be involved in workshop-based fabrication as well as occasional site work, contributing to the assembly and installation of steel structures. Key Responsibilities <ul><li>Perform MIG, TIG, and Stick welding to a high standard</li><li>Fabricate and assemble steel components in line with technical drawings</li><li>Read and interpret engineering drawings and specifications</li><li>Carry out quality checks on fabricated and welded components</li><li>Operate fabrication equipment including cutting, bending, and shaping tools</li><li>Work collaboratively with engineers and team members</li><li>Follow all health & safety procedures</li><li>Assist with on-site installation and project work as required</li></ul> Requirements <ul><li>Proven experience as a Fabricator/Welder or similar role</li><li>Strong welding skills across MIG, TIG, and Stick</li><li>Ability to read and interpret technical drawings</li><li>Experience using fabrication tools and workshop machinery</li><li>High attention to detail and quality</li><li>Strong teamwork and communication skills</li><li>Willingness to travel for site-based work when required</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purposes.

Metal Fabricator / Welder

Engineering Working Foreman A well-established and growing engineering company is seeking an experienced Engineering Working Foreman to lead workshop operations. This is a hands-on role suited to someone who thrives in a fast-paced fabrication environment and enjoys working alongside their team while driving productivity and quality. The Role You will take ownership of workshop production from planning through to completion, ensuring all work is delivered efficiently, safely, and to a high standard. This position requires a balance of leadership and practical skills, with a strong focus on teamwork and continuous improvement. Key Responsibilities <ul><li>Lead by example, actively participating in fabrication and mechanical fitting tasks</li><li>Plan and coordinate daily production activities to meet project deadlines</li><li>Delegate tasks effectively and monitor progress across multiple jobs</li><li>Identify and implement process improvements to increase efficiency</li><li>Carry out quality checks to ensure all work meets required specifications</li><li>Provide regular production updates and reports to management</li><li>Ensure all equipment is maintained and operating safely</li><li>Troubleshoot and resolve any production issues promptly</li><li>Maintain a safe, clean, and organised workshop environment</li></ul> Requirements <ul><li>Minimum 5 years’ experience in steel fabrication, including leadership or supervisory experience</li><li>Strong hands-on skills in welding, fabrication, and mechanical fitting</li><li>Ability to read and interpret technical drawings</li><li>Proven ability to manage workloads and meet tight deadlines</li><li>Strong leadership and team management skills</li><li>Good organisational and problem-solving abilities</li><li>Basic computer skills and willingness to learn new systems</li><li>Fluent English and eligibility to work in Ireland</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Engineering Workshop Foreman

Job Title:     Warehouse Supervisor Location:     Limerick Status:      Permanent Position Summary: <ul><li>As the Warehouse Supervisor you will provide effective and efficient support to Warehouse Policies and Practices and ensure that safe systems of work and practice are maintained through Health & Safety Management</li></ul>  Key Responsibilities: <ul><li>Day to day supervision of the Warehouse and assist warehouse operatives with the day to day duties.</li><li>Drive Quality policies and ensure compliance. Drive staff compliance with operating procedures and SOP updates within area</li><li>Consult with multiple stakeholders of the organisation including suppliers, transport companies, internal and external personnel etc.</li><li>Perform goods inwards & outwards tasks which will require loading and unloading the racking system with product pallets. </li></ul>Qualifications and Requirements: <ul><li>Experience working in a Warehouse environment.</li><li>Relevant mechanical lifting equipment licence desirable.</li><li>Strong Leadership and Organisational skills.</li><li>Computer literate - knowledge of SAP Application an advantage.</li></ul>  For a confidential conversation about the position 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

Warehouse Supervisor

Process / Project Engineer – nPVC Systems & Advanced Manufacturing Location: Castlebar, Ireland Contract: 12‑month contract (potential extension) Role Overview Opportunity for an experienced engineer to support the industrialisation and scale‑up of non‑PVC (nPVC) medical device systems. This role focuses on polymer‑based manufacturing, container‑closure systems, capital equipment, and validation within a regulated environment. Key Responsibilities Technical & Process Development <ul><li>Lead design transfer and industrialisation of nPVC bags, ports, connectors, and assemblies.</li><li>Support conversion from PVC to nPVC materials and multilayer film technologies.</li><li>Provide expertise in sealing, forming, and container‑closure integrity.</li></ul>Capital Equipment & Automation <ul><li>Define URS for new/modified equipment (bag porting, connector welding, automated assembly).</li><li>Support vendor engagement, FAT/SAT, installation, and commissioning.</li><li>Ensure equipment scalability and alignment with automation needs.</li></ul>Validation & Compliance <ul><li>Lead IQ/OQ/PQ for new and modified processes.</li><li>Support sterilisation validation and equivalency strategies.</li><li>Prepare and approve GMP‑compliant documentation (protocols, reports, risk assessments).</li></ul>Regulatory Support <ul><li>Contribute to regulatory‑critical changes (supplier qualification, material changes, E&L, biocompatibility).</li><li>Ensure technical justifications are audit‑ready.</li></ul>Cross‑Functional Collaboration <ul><li>Work with Manufacturing, Quality, R&D, Procurement, Regulatory, and suppliers.</li><li>Support alignment across global sites and lead structured problem‑solving.</li></ul>Requirements Essential <ul><li>Level 8 degree in Mechanical, Polymer, Biomedical, Manufacturing Engineering, or similar.</li><li>5 years in Medical Device, Pharma, or regulated manufacturing.</li><li>Strong polymer manufacturing experience (films, extrusion, moulding, packaging).</li><li>Proven capital project delivery and process validation (IQ/OQ/PQ).</li><li>Knowledge of SPC, DOE, OEE, and process optimisation.</li></ul>Desirable <ul><li>Experience with nPVC systems, multilayer films, or polyolefin elastomers.</li><li>Experience with sterile bag‑based products or dialysis systems.</li><li>Knowledge of sealing technologies, container‑closure integrity, and sterile packaging.</li><li>Exposure to E&L, biocompatibility, and regulatory‑impacting changes.</li></ul>Skills & Attributes <ul><li>Strong technical judgement and hands‑on problem‑solving.</li><li>Effective communicator with cross‑functional teams.</li><li>Self‑driven, organised, and comfortable in fast‑moving environments.</li><li>Excellent documentation discipline.</li></ul>

Project Process Engineer - Contract

Overview An exciting opportunity has arisen for a Building/Office Receptionist  to join a property management team responsible for the day-to-day operation of a modern commercial office development and wider mixed-use estate. The role combines front-of-house reception duties with property management and administrative support. It would suit an organised, proactive individual with at least one year’s experience in administration, facilities, or commercial property management. Key Responsibilities:  Front of House & Administration <ul><li>Act as the first point of contact for visitors, clients, and staff</li><li>Professionally welcome guests, provide information, and direct them appropriately</li><li>Manage reception operations and maintain a professional front-of-house environment</li><li>Schedule appointments, coordinate meetings, and manage meeting room bookings</li><li>Handle general administrative tasks including filing, data entry, and ordering supplies</li><li>Manage incoming and outgoing post and deliveries</li></ul> Property & Facilities Support <ul><li>Support the Property Manager in the day-to-day management of the building within agreed budgets</li><li>Coordinate planned and reactive maintenance works through a purchase order system</li><li>Assist in preparing annual budgets and reviewing expenditure on a quarterly basis</li><li>Conduct regular site inspections and maintain accurate records and reports</li><li>Liaise with tenants regarding general building operations and queries</li><li>Assist in the implementation and management of ESG (Environmental, Social & Governance) initiatives</li><li>Input and maintain property data on ESG and facilities management platforms</li></ul> Operations & Security <ul><li>Assist in maintaining building security and ensuring access control procedures are followed</li><li>Coordinate with cleaning and maintenance contractors to ensure service standards are met</li><li>Manage access systems, car park facilities, and shared/common areas</li><li>Ensure contractors and visitors are appropriately authorised and inducted where required</li></ul> Person Specification <ul><li>Strong communication and interpersonal skills</li><li>Professional, approachable, and customer-focused manner</li><li>Minimum 1 year experience in administration, facilities, or commercial property environment</li><li>Property or Facilities Management qualification (desirable but not essential)</li><li>Good technical understanding or interest in building/facilities operations</li><li>Excellent IT, organisational, and administrative skills</li><li>Proactive, reliable, and able to use initiative</li><li>Strong ability to prioritise tasks and meet deadlines</li><li>Comfortable managing multiple ongoing responsibilities in a busy environment</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Building Receptionist

Director of Operations Quality Location: Galway (On‑site, Full Time) Role Overview The Director of Operations Quality is responsible for leading and overseeing all quality activities related to manufacturing and supply chain operations. This role provides strategic and hands‑on quality leadership, ensuring that production processes, materials, and products meet all applicable regulatory and quality system requirements. The position requires strong operational oversight, team leadership, and the ability to drive continuous improvement within a fast‑paced, growth‑oriented environment. Key Responsibilities Operational Quality Leadership <ul><li>Lead quality activities at manufacturing sites, including incoming inspection, in‑process controls, final release, and batch record review and disposition.</li><li>Maintain governance over product release and batch record control.</li><li>Implement and enforce in‑process controls and statistical process control (SPC) to improve yield and reduce variability.</li></ul>Team Management <ul><li>Manage, mentor, and develop the on‑site operations quality team.</li><li>Recruit, train, and build a high‑performing quality organization.</li><li>Promote a strong culture of quality across manufacturing operations.</li></ul>Quality Systems & Compliance <ul><li>Approve and control production quality procedures, work instructions, and QC sampling plans.</li><li>Manage deviations, nonconformances, CAPAs, and root cause investigations; ensure timely closure and effectiveness checks.</li><li>Ensure compliance with ISO 13485, MDR/MDD, 21 CFR Part 820, and other applicable regulations.</li><li>Support internal and external audits related to manufacturing; lead responses to operations‑related findings.</li></ul>Validation & Process Control <ul><li>Oversee production‑related validations and qualifications, including process validation, equipment qualification, and environmental controls.</li><li>Ensure validation documentation is audit‑ready and compliant with regulatory expectations.</li><li>Support process changes, scale‑up activities, capacity increases, and the transfer of new products or processes into production.</li></ul>Supplier Quality <ul><li>Drive supplier quality management for production materials, including supplier selection, audits, performance monitoring, and corrective actions.</li><li>Manage incoming quality agreements and ensure supplier‑related issues are addressed effectively.</li></ul>Facility & Environmental Controls <ul><li>Oversee routine sterilization controls and lot release processes.</li><li>Ensure cleanroom control measures are implemented and maintained.</li><li>Lead quality aspects of facility expansion initiatives, ensuring quality requirements are integrated into new manufacturing layouts and workflows.</li></ul>Performance Monitoring <ul><li>Develop and report KPIs related to product quality, scrap/rework, deviations, and CAPA effectiveness.</li><li>Provide regular updates to senior leadership on operational quality performance.</li></ul>Professional Qualifications & Attributes <ul><li>Degree in life sciences, engineering, or a related discipline; advanced degree preferred.</li><li>8 years of experience in medical device quality, with significant hands‑on manufacturing and supplier quality experience.</li><li>Proven leadership experience managing quality teams.</li><li>Strong knowledge of ISO 13485 and relevant regulatory requirements (MDR, 21 CFR Part 820).</li><li>Demonstrated experience with production transfers, process validation, and manufacturing CAPA management.</li><li>Proficient in SPC, FMEA, and root cause analysis tools (8D, Fishbone, 5 Whys).</li></ul>

Director of Operations - Quality

Job Title:    CNC Operator Location:    Galway Status:     Permanent Position Summary:   <ul><li>We are seeking skilled CNC Operators to join a growing engineering team working on advanced industrial machinery platforms.</li><li>As the CNC Operator the role typically involves running precision machining equipment in a manufacturing environment</li></ul>  Key Responsibilities: <ul><li>Set up and operate CNC lathes or milling machines to produce precision parts</li><li>Load raw materials, change tooling, and adjust machine offsets</li><li>Read engineering drawings and specifications</li><li>Troubleshoot minor machine issues and optimise cycle times</li><li>Work with materials like steel, aluminium & stainless steel</li></ul> Qualifications and Requirements: <ul><li>Ability to read blueprints</li><li>Basic machining or CNC experience</li><li>Familiarity with measuring tools and tolerance</li><li>CAM software knowledge ideally</li></ul>  For a confidential conversation about the position 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

CNC Operator

Job Title:     Software Engineer   Location:     Galway Status:      Permanent Position Summary:   <ul><li>We are seeking a skilled Software Engineer – Machine Controls & Connectivity to join a growing engineering team working on advanced industrial machinery platforms.</li><li>This role focuses on the development, optimization, and localization of next-generation machine control systems, combining PLC programming, motion control, and modern connectivity solutions.</li><li>You will play a key role in evolving control platforms while collaborating with international engineering teams.</li></ul>  Key Responsibilities: <ul><li>Develop and optimize PLC software using CODESYS or similar platforms</li><li>Implement and refine motion control systems, including servo integration</li><li>Develop and enhance HMI applications using C# or similar technologies</li><li>Improve usability and workflow for machine operators</li><li>Support integration with external systems (e.g., MES, APIs)</li><li>Work with industrial communication protocols (e.g., OPC UA</li><li>Act as a technical interface between global engineering teams</li></ul> Qualifications and Requirements: Education & Experience: <ul><li>Degree in Electrical Engineering, Automation, Computer Science, Mechatronics, or related field</li><li>Proven experience in industrial automation or machinery environments</li></ul>  Technical Skills: <ul><li>Strong PLC programming experience (CODESYS preferred)</li><li>Solid understanding of motion control, servo systems, and industrial automation</li><li>Experience with C# development for HMI or application software</li><li>Familiarity with version control and structured software development processes</li></ul>  Desirable Skills: <ul><li>Experience with MES integration, REST APIs, or OPC UA</li><li>Exposure to cloud platforms (e.g., AWS)</li><li>Knowledge of machine safety standards and compliance</li></ul>  For a confidential conversation about the position 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

Software Engineer

Job Title:     Mechatronics Engineer   Location:    Galway Status:     Permanent Position Summary: <ul><li>We are seeking a skilled Mechatronics Engineer to design and deliver robot-integrated automation solutions across Europe, with a focus on integrating UR and FANUC robots into industrial machine environments.</li><li>This role is centered on building robust, standardised, and scalable automation systems while ensuring safety, performance, and alignment with European requirements.</li></ul>Key Responsibilities: <ul><li>Develop and support UR and FANUC robot integration with industrial machinery</li><li>Design robot-to-machine interfaces including I/O, safety signals, and sequencing</li><li>Implement industrial communication protocols</li><li>Ensure compliance with CE marking and EU machine safety standards</li><li>Support installation, commissioning, and troubleshooting at customer sites</li><li>Collaborate with global engineering teams to align integration strategies</li></ul> Qualifications and Requirements: <ul><li>Degree in Mechatronics, Robotics, Electrical Engineering, Automation, or related field</li><li>Proven experience integrating industrial or collaborative robots (UR and/or FANUC)</li><li>Strong hands-on experience with robot-to-machine integration and sequencing</li><li>Willingness to travel across Europe</li><li>PLC or C# experience is advantageous</li></ul>  For a confidential conversation about the position 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

Mechatronics Engineer

Job Title:     Facilities Lead Location:    Westmeath Status:     Permanent Position Summary: <ul><li>The successful candidate will lead a small team and take responsibility for maintaining and improving the buildings, grounds, services, and facilities across the site.</li><li>This role is suited to a capable individual with a strong practical background in facilities management or a related discipline, ideally within an industrial or manufacturing environment</li></ul>  Key Responsibilities: <ul><li>Lead, develop, and support a small facilities, maintenance, and cleaning team Coordinate facility repairs, upgrades, and improvement projects</li><li>Lead facilities-related CapEx projects from planning to completion</li><li>Ensure compliance with health & safety legislation, building regulations, and environmental standards</li><li>Manage waste disposal, recycling, and sustainability initiatives</li></ul> Qualifications and Requirements: <ul><li>Practical, hands-on approach</li><li>Strong knowledge of health & safety and regulatory compliance</li><li>Alternatively, SOLAS-accredited trade certification with 5 years’ hands-on experience is desirable</li><li>Qualification or proven experience in Facilities Management, Engineering, Energy Management, or related discipline</li></ul>  For a confidential conversation about the position 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

Facilities Lead

ICT Manager (Management Information Systems) Overview We are seeking an experienced ICT Manager to lead and coordinate all information systems and IT infrastructure activities within a fast-paced, high-volume manufacturing environment. This role will oversee a small IT team and ensure the reliability, security, and continuous improvement of all systems supporting business operations. The successful candidate will combine strong technical expertise with People management/Stakeholder capability and prior experience in an industrial or manufacturing setting, with a key focus on supporting production and automation systems. Key Responsibilities: <ul><li>Plan, prioritize, and manage IT support and maintenance activities to ensure optimal system performance and uptime</li><li>Lead and develop a small IT team, providing guidance, mentoring, and performance management</li><li>Oversee daily IT operations, including help desk support, IMAC/VMAC activities, and incident response</li><li>Manage and maintain IT infrastructure, including LAN/WAN networks, servers, telephony systems, desktops, printers, and scanning devices</li><li>Provide IT and technology support to production and automation lines, including troubleshooting (“firefighting”), system upgrades, and fault analysis to minimise downtime</li><li>Collaborate with cross-functional stakeholders to understand business needs and implement effective IT solutions</li><li>Evaluate, recommend, and implement hardware and software solutions to enhance system capabilities</li><li>Ensure data integrity, cybersecurity, and compliance with relevant legal and regulatory requirements</li><li>Develop and enforce IT policies, procedures, and best practices</li><li>Lead business continuity and disaster recovery planning, including system backups and recovery processes</li><li>Manage system scheduling, data storage, and retrieval functions</li><li>Provide technical leadership on medium to large-scale IT projects</li><li>Support workforce planning, including recruitment and retention of IT staff</li></ul> Requirements <ul><li>Bachelor’s degree in IT, Computer Science, or a related field (or equivalent experience)</li><li>Minimum of 6 years’ experience in IT, with proven Senior / Management responsibility</li><li>Previous experience in a manufacturing or industrial environment is essential</li><li>Experience supporting production systems, automation lines or shop-floor IT environments</li><li>Strong knowledge of IT infrastructure, including networks, servers, and end-user support</li><li>Demonstrated ability to troubleshoot complex system issues in time-critical production environments</li><li>Proven experience in system upgrades, fault diagnosis, and continuous improvement initiatives</li><li>Strong problem-solving skills and ability to work independently</li><li>Excellent communication and stakeholder management skills</li></ul> Key Competencies <ul><li>Leadership and team development</li><li>Strategic thinking and decision-making</li><li>Technical expertise across IT systems and infrastructure</li><li>Project management</li><li>Process improvement and operational efficiency</li><li>Ability to operate effectively in a fast-paced, production-driven environment</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

ICT Manager

Job Title:     Commercial Finance Business Partner Location:    Monaghan Status:     Contract Position Summary: <ul><li>Act as a primary link between finance and the commercial team, providing insight to support decision-making and guidance to optimise customer profitability and sales growth.</li><li>Share insights with the leadership team on retailer performance and performance to budget</li><li>Reporting to the Chief Financial Officer, the Commercial Finance Business Partner will support the commercial team to achieve objectives on volume, pricing and profitability across our key retailers.</li></ul>  Key Responsibilities: <ul><li>Act as a trusted advisor to the Commercial Director and the account managers</li><li>Assist with the budgeting process, tracking monthly on key metrics by retailer</li><li>Develop tools and dashboards to bring real clarity to monthly customer profitability</li><li>Provide financial insight guidance to support negotiations with key customers</li></ul> Qualifications and Requirements: <ul><li>Qualified Accountant</li><li>Experience within FMCG</li><li>Commercial Finance experience</li><li>Analytical and financial modelling skills</li></ul>For a confidential conversation about the position 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

Commercial Finance Business Partner

We are seeking a detail-oriented and proactive Accounts Payable Specialist to join our clients growing finance team. This is an exciting opportunity to play a key role in supporting day-to-day finance operations within a fast-paced and evolving business environment. This position will take ownership of the accounts payable function while working closely with the wider finance team to support business growth and operational efficiency. Key Responsibilities: <ul><li>Manage the end-to-end accounts payable process, including verification, coding, and timely processing of invoices</li><li>Prepare and execute payment runs to vendors</li><li>Respond to vendor queries, resolve discrepancies, and maintain strong working relationships</li><li>Monitor and manage the accounts payable inbox, ensuring timely handling of all incoming invoices and requests</li><li>Process employee expense claims in line with company policies</li><li>Review and maintain the Purchase Order (PO) log to ensure accuracy and completeness</li><li>Ensure compliance with internal controls, accounting policies, and relevant tax regulations</li><li>Support month-end and year-end close processes related to accounts payable and receivable</li><li>Contribute to process improvements, system enhancements, and workflow efficiencies</li><li>Assist with finance-related projects, including ERP system implementation and business expansion initiatives</li><li>Provide ad hoc support to the wider finance team as required</li><li>Support accounts receivable activities as the role evolves</li></ul> Requirements: <ul><li>Proven experience in an Accounts Payable or Accounts Receivable role within a fast-paced environment</li><li>Strong understanding of accounts payable processes and core accounting principles</li><li>Experience working with ERP or accounting systems (e.g., QuickBooks, NetSuite, Odoo)</li><li>Excellent attention to detail with the ability to manage high volumes of transactions accurately</li><li>Strong organisational and time management skills</li><li>Ability to quickly learn new systems and processes</li><li>Effective communication skills, with the ability to engage confidently with internal stakeholders and external vendors</li><li>Self-motivated, adaptable, and able to thrive in a dynamic environment</li></ul> Desirable <ul><li>Experience working in a start-up or high-growth environment</li><li>Exposure to the medical devices or similar regulated industry</li><li>Experience with SAP Concur or similar expense management systems</li><li>Accounts Receivable experience</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Accounts Payable Specialist

Senior Manufacturing Supervisor – Medical Devices About the Role We are currently recruiting on behalf of our client for an experienced Senior Manufacturing Supervisor to lead operations within a regulated medical device environment. This is a key leadership role responsible for driving production performance, ensuring regulatory compliance, and developing high-performing teams in a fast-paced manufacturing setting. Key Responsibilities <ul><li>Lead daily manufacturing operations to achieve targets across safety, quality, delivery, and cost</li><li>Supervise and develop production teams including supervisors, team leads, trainers, and operators</li><li>Coordinate production planning to meet customer demand</li><li>Ensure full compliance with GMP, ISO 13485, and FDA regulations</li><li>Partner with Engineering, Quality, and Supply Chain to resolve issues and improve processes</li><li>Drive continuous improvement initiatives using Lean and Six Sigma methodologies</li><li>Monitor KPIs and implement corrective actions where required</li><li>Support new product introductions (NPI) and technology transfers</li><li>Maintain accurate documentation and ensure product traceability</li><li>Lead internal and external audits related to production</li><li>Manage staffing levels and resource planning based on demand</li><li>Conduct regular Gemba walks to ensure adherence to Health & Safety, Quality, and operational standards</li></ul> Requirements <ul><li>Bachelor’s degree in Engineering, Manufacturing, or a related discipline</li><li>5 years’ experience in a medical device or highly regulated manufacturing environment</li><li>Strong knowledge of GMP, ISO 13485, and FDA requirements</li><li>Proven leadership experience with the ability to develop and motivate teams</li><li>Experience with Lean Manufacturing, Six Sigma, or continuous improvement tools</li><li>Excellent communication, problem-solving, and organisational skills</li></ul> Desirable <ul><li>Experience with ERP systems such as SAP, Oracle, or IFS</li><li>Exposure to advanced manufacturing technologies</li><li>Strong interpersonal skills with the ability to influence and drive change</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Senior Supervisor

Quality Engineer - Contract Role Location: Client Medical Device Manufacturing Site Shift: Primarily Day Shift (Flexibility Required for Occasional Evening Shifts) Contract Type: Contract Position Job Summary The Quality Engineer will ensure that all products manufactured at the client’s medical device site comply with approved specifications and that all site activities adhere to current Good Manufacturing Practice (cGMP) and applicable regulatory requirements. Working as part of the Quality Team, the successful candidate will support the achievement of quality objectives and ensure ongoing compliance with internal procedures and external regulatory standards. Key Responsibilities <ul><li>Coordinate assigned elements of the Quality Management System (QMS), ensuring full compliance across site operations</li><li>Participate in internal and external quality audits as required</li><li>Support the investigation of customer complaints and implement effective corrective and preventive actions (CAPA)</li><li>Manage day-to-day CAPA activities, ensuring timely initiation, investigation, and closure</li><li>Monitor and report on Quality System performance metrics for management review</li><li>Deliver quality-related training to site personnel as required</li><li>Escalate quality system failures and support implementation of corrective actions and product containment</li><li>Verify effectiveness of corrective and preventive actions</li><li>Ensure compliance with all applicable regulatory requirements (e.g., ISO, FDA)</li><li>Support validation activities across manufacturing processes</li><li>Maintain accurate, complete, and compliant Quality System documentation</li><li>Review lot/batch records and perform product release activities</li><li>Inspect incoming materials and support supplier quality management</li><li>Perform in-process and final product testing in line with approved specifications</li><li>Participate in continuous improvement initiatives across quality, safety, and production systems</li><li>Support risk management activities as required</li></ul> Essential Requirements <ul><li>Degree in Engineering, Science, Quality, or a related discipline</li></ul> Desirable Requirements <ul><li>Lean Six Sigma Green Belt or equivalent statistical knowledge</li><li>Experience in injection moulding or tooling environments</li></ul> Experience Required <ul><li>Minimum 2 years’ experience working within a Quality function in a highly regulated medical device or combination product manufacturing environment</li><li>Working knowledge of quality system regulations such as ISO 13485, ISO 9000, and/or FDA 21 CFR Part 820</li><li>Experience with key quality system elements such as CAPA, auditing, validation, and design controls</li></ul> Key Skills & Competencies <ul><li>Strong attention to detail with a high level of accuracy</li><li>Proven problem-solving and analytical skills</li><li>Ability to adapt to changing processes and priorities</li><li>Strong technical aptitude within a manufacturing environment</li><li>Commitment to quality, compliance, and safety</li><li>Ability to work independently with a high level of initiative</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Quality Engineer

Role Overview We are seeking an experienced and motivated OpEx Business Analyst to join our clients global Operational Excellence team. This role focuses on designing, developing, and maintaining interactive dashboards and data-driven solutions to support business optimisation initiatives. The successful candidate will play a key role in transforming complex data into clear, actionable insights using modern digital tools, primarily Microsoft Power BI and the wider Microsoft Power Platform ecosystem. You will collaborate with cross-functional teams across Dublin, Puerto Rico, and the US to support data-driven decision-making and continuous improvement initiatives. Key Responsibilities <ul><li>Gather and translate stakeholder requirements into effective dashboard and reporting solutions.</li><li>Design, develop, and maintain interactive dashboards using Power BI and other approved digital tools.</li><li>Build and manage data models, integrating multiple data sources such as SQL Server, SharePoint, and Dataverse.</li><li>Apply data visualization best practices to present insights clearly, including drill-throughs and advanced analytics.</li><li>Collaborate with business users, data analysts, and IT teams to ensure accuracy and consistency of data.</li><li>Optimise dashboards for performance, usability, and scalability.</li><li>Publish and maintain reports and dashboards for stakeholder access.</li><li>Provide training and support to end users on dashboard usage and interpretation.</li><li>Support automation and process improvement initiatives using Power Platform tools</li></ul>Experience <ul><li>Minimum 18 months’ experience in a similar data/digital role.</li><li>Strong experience with Microsoft Power BI.</li><li>Working knowledge of PowerApps, Power Automate, and Dataverse.</li><li>Experience with SQL Server and relational databases.</li><li>Familiarity with SharePoint and data integration techniques.</li><li>Knowledge of JSON, HTML, and basic C .</li><li>Experience using development tools such as Visual Studio Code or Visual Studio.</li><li>Exposure to Power Platform CLI.</li><li>Programming experience in one or more: JavaScript, TypeScript, React JS, Python.</li></ul> Deliverables <ul><li>Operational metrics dashboards</li><li>Balanced scorecard reports</li><li>Qualification and compliance reports</li><li>Automation usage and performance dashboards</li><li>Integrated survey and reporting tools</li><li>Training materials and end-user support sessions</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Business Analyst - OpEx

QA Validation Engineer Department: Quality Reporting to: Validation Team Lead Overview We are seeking a QA Validation Engineer to support the site validation program, ensuring compliance with regulatory, quality, and cGMP standards within a biopharmaceutical manufacturing environment. Key Responsibilities <ul><li>Support and execute validation activities for equipment, utilities, processes, and systems</li><li>Develop and maintain:<ul><li>Validation Master Plan (VMP)</li><li>Project validation plans and schedules</li></ul></li><li>Generate and execute:<ul><li>Validation protocols (IQ/OQ/PQ)</li><li>Final reports and investigations</li></ul></li><li>Manage change control, deviations, and CAPA processes</li><li>Review and approve validation and quality documentation</li><li>Ensure all activities are completed in line with cGMP and regulatory requirements</li><li>Support audits (internal and external)</li><li>Contribute to continuous improvement initiatives across quality and manufacturing</li><li>Maintain compliance across production areas and support cross-functional teams</li></ul>Requirements <ul><li>Degree in Engineering or a scientific discipline</li><li>Minimum 3 years’ experience in validation within a regulated (biopharma/pharma) environment</li><li>Strong knowledge of:<ul><li>cGMP</li><li>Validation lifecycle (IQ/OQ/PQ)</li><li>Regulatory standards (FDA / EU GMP / GAMP)</li></ul></li><li>Excellent communication, organisation, and problem-solving skills</li><li>Ability to work independently and within cross-functional teams</li></ul>Key Competencies <ul><li>Strong attention to detail with a Right First Time mindset</li><li>Ability to manage multiple priorities and meet deadlines</li><li>Proactive approach to issue resolution and compliance</li></ul>Additional Information <ul><li>High level of autonomy with responsibility for delivering validation activities</li><li>Regular interaction with internal teams and external auditors</li><li>Commitment to maintaining safety, quality, and compliance standards at all times</li></ul>

QA Validation Engineer

Project (Automation) Engineer Location: Westport Duration: 12-month initial contract (with strong extension potential) Overview We are seeking a Project (Automation) Engineer to support a large-scale Electronic Batch Record (EBR) implementation project within a pharmaceutical manufacturing environment. This role will focus on transitioning plant operations from traditional paper-based batch records to fully digital EBR systems, working as part of a cross-functional automation project team. Key Responsibilities <ul><li>Lead scoping and requirements definition for EBR implementation across manufacturing areas</li><li>Assess equipment readiness and identify requirements for EBR conversion</li><li>Define scope for:<ul><li>Software upgrades</li><li>PLC network cards</li><li>Operator interfaces (PC carts, tablets)</li><li>WiFi access points, LAN infrastructure, and power requirements</li></ul></li><li>Develop cost estimates, including installation and potential qualification activities</li><li>Prepare and present project scope, timelines, and budgets to stakeholders</li><li>Raise purchase orders and coordinate with vendors and contractors</li><li>Work closely with Production to plan access for installation and upgrades</li><li>Act as Permit Requester, ensuring:<ul><li>Risk assessments</li><li>Method statements</li><li>EHS compliance</li></ul></li></ul>Automation & Systems Integration <ul><li>Assess and scope connectivity to the Manufacturing Control Network (MCN)</li><li>For networked equipment:<ul><li>Identify required data fields from PLC/SCADA systems</li><li>Support integration into OSIsoft PI System</li><li>Collaborate with Automation/OT teams to ensure data availability for MES/EBR configuration</li></ul></li><li>Liaise with vendors to obtain and manage PLC/SCADA data tags</li></ul>Project Delivery & Compliance <ul><li>Support engineering lifecycle documentation and system updates</li><li>Participate in project reviews and technical documentation</li><li>Execute engineering activities related to change control processes</li><li>Ensure compliance with GMP and regulated environment standards</li></ul>Key Requirements <ul><li>Degree in Engineering (Automation, Electrical, Chemical, or related discipline)</li><li>Experience in pharmaceutical or regulated manufacturing environments</li><li>Strong background in:<ul><li>Automation systems (PLC/SCADA)</li><li>MES / EBR projects (preferred)</li><li>Industrial networking and system integration</li></ul></li><li>Proven experience in:<ul><li>Project engineering or project delivery</li><li>Vendor and contractor coordination</li><li>Costing, scheduling, and scope management</li></ul></li><li>Familiarity with data historians and manufacturing systems integration is an advantage</li></ul>Desirable <ul><li>Experience with EBR/MES platforms (e.g., POMS)</li><li>Knowledge of validation / qualification processes (CSV)</li><li>Understanding of GMP and change control systems</li></ul>

Project Automation Engineer

Quality Technician We are currently seeking a Quality Technician to join a dynamic and growing team within a highly regulated medical device manufacturing environment. This is an excellent opportunityis an initial 6-Month Contract (with view to extension) and would suit a detail-oriented professional who will contribute to quality excellence and continuous improvement initiatives. Key Responsibilities: <ul><li>Perform incoming, in-process, and final product inspections/testing in line with approved procedures and specifications</li><li>Ensure all activities are fully compliant with cGMP, ISO, and regulatory requirements</li><li>Support operations across Quality Control (QC), Incoming Quality Assurance (IQA), and Metrology areas</li><li>Maintain accurate and compliant quality documentation and records</li><li>Identify, report, and escalate quality issues or potential risks in a timely manner</li><li>Participate in internal audits and support audit readiness activities</li><li>Assist with change control processes, including documentation updates</li><li>Generate and report quality metrics for management review</li><li>Support batch record preparation and manufacturing documentation</li><li>Make disposition decisions on incoming materials</li><li>Contribute to continuous improvement initiatives across quality, safety, and production</li></ul> Requirements: <ul><li>Third-level qualification in a relevant scientific or technical discipline (desirable)</li><li>1–2 years’ experience in a GMP-regulated environment (medical devices, pharma, or similar)</li><li>Experience working within a quality system in a regulated manufacturing environment</li><li>Strong understanding of GMP, ISO, and regulatory standards</li></ul> Key Skills & Competencies: <ul><li>Exceptional attention to detail and accuracy</li><li>Strong problem-solving and analytical skills</li><li>Ability to work independently and as part of a team</li><li>Adaptable and comfortable working in a fast-paced, regulated environment</li><li>Strong commitment to quality, compliance, and safety</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Quality Technician

Project (Automation) Engineer We are currently seeking an experienced Project (Automation) Engineer to join a dynamic and growing engineering team. This is an exciting opportunity to work on a range of high-impact projects involving automation, aseptic processing, and manufacturing equipment within a regulated environment. Key Responsibilities: <ul><li>Coordinate the delivery of processing equipment to site in line with project scope and timelines</li><li>Oversee equipment installation and service hook-ups in collaboration with vendors and engineering teams</li><li>Support or lead Factory Acceptance Testing (FAT) activities</li><li>Ensure all equipment documentation is completed and maintained</li><li>Commission equipment in preparation for validation activities</li><li>Develop training materials and maintenance protocols</li><li>Report project progress and provide technical support to the Project Manager</li><li>Contribute to cross-functional problem-solving in manufacturing, aseptic processing, and packaging</li><li>Drive process improvement initiatives across the business</li><li>Lead project review meetings and participate in regular operational and departmental meetings</li></ul> Requirements: <ul><li>Degree qualification in Engineering, Automation, Science, or a related discipline</li><li>Minimum of 5 years’ experience in a relevant engineering role</li><li>Experience in medical device or pharmaceutical industries is advantageous but not essential</li><li>Project management experience is desirable</li><li>Strong interpersonal skills with the ability to work in cross-functional teams</li><li>Ability to work independently and manage multiple priorities</li></ul> Skills & Experience: <ul><li>Strong organisational and time management skills</li><li>Experience working on equipment or process-related projects</li><li>Exposure to regulated environments (GxP/GMP) preferred</li><li>Familiarity with manufacturing systems</li><li>Knowledge of PLC and SCADA systems</li><li>Proficient in Microsoft Office and Windows platforms</li><li>Flexible approach to support production needs when required</li><li>Willingness to learn and adapt to new technologies</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Project Engineer III

Documentation Specialist (Laboratory) We are seeking a detail-oriented Documentation Specialist to support laboratory operations in a regulated environment. This role is critical in ensuring documentation meets GMP/GDP compliance and is delivered on time to support manufacturing and quality objectives. Key Responsibilities:  <ul><li>Coordinate review and approval of laboratory documentation (SOPs, logbooks, forms)</li><li>Ensure documents progress efficiently through approval workflows in line with timelines</li><li>Maintain and manage documentation within electronic systems</li><li>Act as a key point of contact for document status and process queries</li><li>Support laboratory readiness for NPI, Tech Transfer, and routine manufacturing</li><li>Review, edit, and format documents to ensure accuracy and compliance (GMP/GDP)</li><li>Track and report on documentation metrics and performance</li><li>Participate in investigations, root cause analysis, and continuous improvement initiatives</li><li>Collaborate cross-functionally to ensure consistency and compliance</li></ul> Requirements:  <ul><li>Bachelor’s degree (preferably in Science or related field)</li><li>1 year experience in a regulated laboratory or document control environment</li><li>Strong knowledge of GMP/GDP standards</li><li>Proficiency in Microsoft Word, Excel, PowerPoint, Outlook, Visio</li><li>Experience with electronic document management systems preferred</li><li>Excellent attention to detail, organisation, and communication skills</li><li>Ability to work in a fast-paced, deadline-driven environment</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Documentation Specialist

We are seeking a motivated and detail-oriented QC Analyst to join a dynamic analytical laboratory team operating within a regulated environment. This role is ideal for someone with hands-on laboratory experience who is passionate about quality, data integrity, and continuous improvement. You will play a key role in ensuring timely and compliant analytical testing, supporting investigations, and driving operational excellence within the lab. Key Responsibilities:  <ul><li>Ensure laboratory documentation and computerized systems comply with Data Integrity and regulatory requirements</li><li>Perform and complete analytical testing in line with agreed schedules</li><li>Support and guide team members to ensure high standards of test execution and performance</li><li>Drive continuous improvement initiatives to enhance laboratory efficiency and productivity</li><li>Monitor testing schedules and implement recovery plans where required</li><li>Identify performance gaps and collaborate with management on corrective actions</li><li>Initiate and support Out of Specification (OOS) investigations in a timely manner</li><li>Maintain accurate, complete, and compliant laboratory records</li><li>Ensure laboratory equipment is properly used, calibrated, and maintained</li><li>Promote a strong quality culture and adherence to 5S standards</li><li>Investigate documentation-related events with potential quality or compliance impact</li><li>Participate in or lead investigation activities such as root cause analysis</li><li>Collaborate cross-functionally and communicate technical information effectively</li><li>Ensure compliance with internal procedures and all applicable regulatory standards</li></ul> Requirements:  <ul><li>Bachelor’s degree (or equivalent) in a Science or related discipline (preferred)</li><li>Minimum 1 years’ experience in an analytical or QC laboratory role</li><li>Experience working in a GLP/GMP-regulated environment</li><li>Strong knowledge of EU, FDA, ICH, and HPRA guidelines</li><li>Hands-on experience with analytical instrumentation (e.g., UHPLC, SoloVPE, TOC)</li><li>Proven ability to troubleshoot laboratory equipment and methods</li><li>Strong attention to detail with excellent problem-solving skills</li><li>Effective communication and teamwork abilities</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

QC Analytical Analyst

Research Scientist Role Overview Hands-on, research-focused role responsible for generating preclinical and clinical evidence to support medical device development. The position centres on experimental design, data analysis, and scientific publication, with a strong emphasis on translating research into clinical impact. Key Responsibilities Research & Evidence Generation <ul><li>Design, execute, and analyse preclinical experiments</li><li>Conduct in-vitro and benchtop testing (e.g., occlusion models)</li><li>Maintain accurate, compliant experimental records and datasets</li><li>Interpret results and communicate findings to internal and clinical teams</li></ul>Scientific Communication <ul><li>Lead and support preparation of peer-reviewed publications</li><li>Contribute to clinical research activities (first-in-human and post-market studies)</li><li>Present findings internally and at external conferences</li><li>Support scientific content for training and commercial activities</li></ul>Collaboration <ul><li>Work closely with multidisciplinary teams and clinical collaborators</li><li>Align research activities with clinical and product needs</li><li>Support conference preparation and coordination</li></ul>Additional Responsibilities <ul><li>Manage research and demonstration devices</li><li>Support sourcing of materials and test equipment</li><li>Provide general scientific and operational support to R&D and clinical teams</li></ul>Required Qualifications & Experience <ul><li>MSc or PhD in Biomedical Engineering, Life Sciences, or related field</li><li>Strong experience in experimental design, execution, and data analysis</li><li>Proven scientific writing skills (peer-reviewed publications preferred)</li><li>Excellent organisational and documentation skills</li><li>Strong communication and teamwork abilities</li></ul>Desirable Experience <ul><li>In-vitro / benchtop model development (cardiovascular or neurovascular preferred)</li><li>Knowledge of stroke or neurovascular therapies</li><li>Experience working with clinicians or clinical research teams</li><li>Conference presentation experience</li><li>Familiarity with regulated medical device environments</li></ul>

Reserach Scientist

Project Manager (Contract)  New Connectivity Product Development A growing technology company that develops hardware, software, and connected solutions for safer, healthier, and more sustainable homes is seeking an experienced Project Manager (Contract) to lead the development of a new connectivity product. This organization delivers trusted solutions that help people live independently and safely in their homes. As the company continues to expand its product portfolio, this role will play a key part in bringing innovative products from initial concept through to market launch. This is a daily rate contract position, requiring a highly experienced professional with strong technical and product development expertise.   Key Responsibilities <ul><li>Lead the end-to-end project management of a new connected product solution.</li><li>Manage product development from concept, feasibility, research & development, prototyping, and manufacturing through to market launch.</li><li>Coordinate cross-functional teams including engineering, hardware, software, and manufacturing.</li><li>Support technical feasibility assessments and early-stage product concept development.</li><li>Work closely with external contractors, suppliers, and manufacturing partners.</li><li>Monitor project timelines, budgets, risks, and deliverables.</li><li>Ensure alignment between technical development, product strategy, and commercial launch plans.</li><li>Provide strong leadership and clear communication across internal and external stakeholders.</li></ul>  Required Experience <ul><li>Proven Project Management experience delivering electronic products.</li><li>Demonstrated experience managing electronics-based product development from concept through to launch.</li><li>Strong Research & Development (R&D) background.</li><li>Experience working with hardware and electronics engineering teams.</li><li>Strong engineering understanding or technical aptitude.</li><li>Experience managing large, complex projects with multiple stakeholders.</li><li>Experience working with external contractors and manufacturing partners.</li></ul>  Skills & Attributes <ul><li>Self-starter with strong initiative and ownership.</li><li>Excellent leadership and stakeholder management skills.</li><li>Strong analytical and problem-solving abilities.</li><li>Highly organized with strong project planning capability.</li><li>Comfortable working in a fast-paced, innovative environment.</li></ul>  Working Arrangements <ul><li>Daily rate contract position.</li><li>Flexibility required to attend sites and offices across the UK when needed.</li><li>Opportunity to work on innovative technology that improves safety, health, and sustainability in the home.</li></ul>

Project Manager

Senior Design Assurance Quality Engineer Role Summary The purpose of this role is to provide Design Control and Quality Engineering support for medical device products within a manufacturing environment. The position supports product development, regulatory compliance, and manufacturing quality, contributing to the successful commercialization of products and overall business growth. Key Responsibilities Design Assurance & New Product Development <ul><li>Act as the Quality representative and core team member on New Product Commercialization (NPC) projects.</li><li>Lead and support Design Control activities, ensuring compliance with applicable regulatory and quality standards.</li><li>Facilitate risk management activities, including Risk Assessments and Design Failure Mode and Effects Analysis (DFMEA).</li><li>Support the development and review of product specifications, engineering drawings, and technical documentation.</li></ul>Process & Manufacturing Support <ul><li>Contribute to Process Failure Mode and Effects Analysis (PFMEA) and process validation activities for new product introduction projects.</li><li>Provide quality guidance and oversight during product and process development.</li></ul>Quality Systems & Compliance <ul><li>Perform internal audits in accordance with the annual audit schedule to ensure compliance with ISO 13485 and FDA Quality System Regulations (QSR).</li><li>Ensure design and development activities meet all applicable regulatory and quality requirements.</li></ul>Problem Solving & Continuous Improvement <ul><li>Support Corrective and Preventive Action (CAPA) investigations and implement effective solutions related to new product projects and manufacturing processes.</li><li>Perform statistical analysis to support validation activities and continuous improvement initiatives.</li></ul>Training & Support <ul><li>Provide training and guidance to personnel on quality procedures, design controls, and regulatory requirements as required.</li></ul>Experience Requirements <ul><li>5–8 years of experience in the medical device industry.</li><li>Demonstrated experience with:<ul><li>Design Controls</li><li>New Product Introduction (NPI/NPC)</li><li>Statistical analysis</li><li>Process validation</li></ul></li></ul>Education & Qualifications <ul><li>Bachelor’s degree in Engineering or a related Science discipline.</li><li>Professional quality qualification preferred, such as Certified Quality Engineer (CQE).</li><li>Experience working in regulated environments aligned with ISO 13485 and FDA requirements.</li></ul>

Senior Design Assurance Engineer

Design Assurance Manager – Galway Role Summary The Design Assurance Manager is responsible for ensuring medical devices are designed and developed in compliance with applicable regulatory requirements and quality standards. This role provides leadership across design controls, risk management, and verification and validation activities throughout the product lifecycle, while partnering closely with cross-functional teams. Key Responsibilities <ul><li>Own and maintain design control processes in compliance with ISO 13485, EU MDR, and FDA 21 CFR 820.</li><li>Ensure complete and compliant Design History Files (DHF) and design documentation.</li><li>Lead risk management activities in accordance with ISO 14971.</li><li>Oversee design verification and validation, including usability engineering where applicable.</li><li>Support design transfer to manufacturing and related validation activities.</li><li>Provide design assurance input to design changes, CAPAs, complaints, and post-market activities.</li><li>Support regulatory submissions and audits (Notified Body, FDA, internal).</li></ul>Qualifications & Experience <ul><li>Bachelor’s degree in Engineering, Science, or related field.</li><li>5 years experience in design assurance, quality, or regulatory roles within the medical device industry.</li><li>Strong working knowledge of ISO 13485, ISO 14971, EU MDR, and FDA design controls.</li><li>Experience supporting audits and regulatory submissions.</li></ul>Key Skills <ul><li>Strong attention to detail and documentation skills</li><li>Effective cross-functional communication</li><li>Risk-based decision making</li><li>Ability to work independently in a regulated environment</li></ul>

Design Assurance Manager

About the Role An established manufacturing company is seeking an experienced NPI & Quotation Engineer to join the team at its facility in Shannon, Co. Clare. In this key role, you will act as the link between customer requirements and production planning, ensuring accurate quotations and supporting efficient communication between internal teams and suppliers. About the Company The company specializes in the manufacture of precision metal components and assemblies tailored to meet exact customer specifications. With a skilled workforce and a strong reputation for quality, the organisation delivers high-quality manufacturing solutions to clients worldwide. Operating under ISO9001 and AS9100 quality standards, the company maintains rigorous processes and industry best practices to ensure the highest levels of performance and customer satisfaction. Key Responsibilities <ul><li>Translate customer information into practical working formats for the quotation office</li><li>Prepare Bills of Materials (BOMs) and component specifications using Excel for supplier distribution</li><li>Respond to supplier queries regarding parts and specifications</li><li>Collaborate with Finance, NPI, and Engineering teams to develop and improve labour costings</li><li>Monitor labour efficiency against quoted timelines</li><li>Develop and implement effective costing models</li><li>Work closely with the Sales team and customers to deliver quotations in a timely and professional manner</li><li>Monitor foreign exchange (FX) rates to ensure accurate cost projections</li><li>Interpret and understand detailed engineering drawings</li><li>Liaise with suppliers to track and manage component costs</li><li>Maintain and oversee the Approved Vendor List (AVL)</li><li>Upload and maintain BOMs and routers within the ERP system</li><li>Provide administrative support to both the Sales and Engineering teams</li></ul> Requirements <ul><li>Engineering background is essential</li><li>Sheet metal manufacturing experience is essential</li><li>Experience in cost modelling and supplier management is advantageous</li><li>Finance or costing experience is desirable</li><li>Strong analytical and organisational skills</li><li>Advanced Excel skills and experience with ERP systems</li><li>Ability to interpret engineering drawings</li><li>Excellent communication and problem-solving abilities</li><li>Previous experience in NPI (New Product Introduction) or quotation engineering roles is highly desirable</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

NPI & Quotation Engineer

Job Overview: We are seeking a skilled Manufacturing Execution Systems (MES) Specialist to support the design, implementation, and continuous improvement of MES recipes and system processes. The successful candidate will ensure compliance with regulatory, quality, safety, and operational standards while supporting manufacturing and new product introduction activities. Key Responsibilities: <ul><li>Design, develop, and maintain POMSnet MES recipes and system configurations.</li><li>Manage and implement MES system changes aligned with business and operational objectives.</li><li>Support SAP and MES strategy implementation within manufacturing operations.</li><li>Ensure MES processes, SOPs, policies, and training materials comply with current safety, quality, and IT standards.</li><li>Review and manage business and system risks associated with MES and recipe changes.</li><li>Support timely and compliant qualification of MES recipes, upgrades, and system enhancements.</li><li>Act as local key user (LKU) for SAP and MES systems, supporting material and system queries.</li><li>Participate in project activities from initiation through implementation to ensure system and hardware requirements are addressed.</li><li>Troubleshoot and resolve MES, recipe, and system-related issues in collaboration with cross-functional teams.</li><li>Prepare and present project and system status reports.</li><li>Participate in Technical Review Boards and support identification of issues, workarounds, and system fixes.</li><li>Support regulatory audits and inspections from authorities and customers.</li><li>Promote a culture of right-first-time performance and continuous improvement.</li><li>Participate in MES knowledge sharing and cross-site collaboration initiatives</li></ul>Qualifications & Experience: <ul><li>Third level qualification in Science, Engineering, IT, or a related discipline (Certificate, Diploma, or Degree).</li><li>Minimum of 3 years’ experience working in a regulated manufacturing environment (FDA/HPRA or equivalent).</li><li>Strong knowledge of cGMP and pharmaceutical regulatory requirements.</li><li>Experience working with MES systems (POMSnet or similar platforms preferred).</li><li>Experience supporting SAP systems is advantageous.</li></ul>Skills & Competencies:  <ul><li>Strong technical and problem-solving abilities.</li><li>Excellent organisational and time management skills.</li><li>Ability to manage multiple priorities in a fast-paced manufacturing environment.</li><li>Strong communication and interpersonal skills with the ability to collaborate across teams.</li><li>High level of integrity and strong work ethic.</li><li>Demonstrated ability to drive performance improvement initiatives.</li></ul> For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

MES Engineer

<h1>OUR BLOG</h1>

Related Blogs

<h1>US corporate engineering</h1>

Related Case study

Industries We Serve

<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. 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;">&nbsp;</h1><h1 style="text-align: center;">&nbsp;</h1><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 services enable companies to save time, 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.

This is a 404 error, which means you've clicked on a bad link or entered an invalid URL.

<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

One click could change everything. Submit your CV today.

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 style="text-align: center;">&nbsp;</h1><h1 style="text-align: center;">&nbsp;</h1><h1 style="text-align: center;">Privacy Policy</h1>

<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&rsquo;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 Owen&nbsp;
Owen Clancy is a recruitment consultant, specialising in engineering and life science talent. He manages the full recruitment lifecycle, working closely with clients and candidates to deliver strong hiring outcomes and a transparent experience.&nbsp;
With a background in HR and as an Associate CIPD member, he brings a people-focused, professional approach baked by experience in talent acquisition, employee relations and HR operations.&nbsp;
He focuses on building long-term relationships and regularly recruits for technical roles across Ireland, including engineering, quality and project management positions.&nbsp;

Owen Clancy 

About Tommy&nbsp;
Tommy McKeown is a senior recruitment consultant specialising in engineering and medical device talent across Ireland. He manages the full recruitment lifecycle, partnering closely with clients and candidates to deliver strong hiring outcomes and a seamless experience.&nbsp;
With over six years' experience in technical recruitment, Tommy brings a results-driven and market-focused approach, backed by deep knowledge of regulated industries including medtech and advanced manufacturing.&nbsp;
He focuses on building long-term relationships and regularly recruits for a wide range of roles, including R&amp;D, quality, project management and senior leadership positions such as VP Operations and Head of Engineering.&nbsp;

Tommy Mckeown

About Aidan
Aidan McNabola is a seasoned engineering professional with over 38 years of leadership experience in engineering and manufacturing, including 16 years specifically in sterile manufacturing across five sites. They have managed both direct and indirect teams of over 50 people and have extensive experience in corporate governance, including remediation, regulatory compliance and inspections. Their background also includes leading greenfield operations from startup through acquisition and overseeing projects ranging from &euro;50,000 to &euro;150 million.
&nbsp;
Career Highlights:
<ul>
<li>
Viatris Pharmaceuticals &ndash; Senior Director of Engineering. (6 years) Managed engineering activities for the Sterile filling operations. Managed the conceptual and detailed design and install of a sterile cartridge filling and assembly line . Capex value 30mill. Euros.
</li>
<li>
Taro Pharma &ndash; Engineering Manager. Managed site engineering activities for a sterile fill finish facility. Conceptual and detailed design for two new Aseptic Fill Finish Lines.
</li>
<li>
Elan Pharma &ndash; Senior Project Manager. Front end study and detailed design for a new Fill Finish facility.
</li>
<li>
Allergan Pharmaceuticals &ndash; Engineering Manager. Design, Build, start up of a new Botox facility 20Mill.
</li>
<li>
GE Healthcare &ndash; Senior Project Manager/Operations. Managed sterile filling operations. Installation of a new sterile bottle filling line and start up operations.
</li>
</ul>
&nbsp;
Education &amp; Qualifications:&nbsp;
<ul>
<li>Degree Mechanical Engineering, University Limerick</li>
<li>Chartered Eng. FIEI.</li>
<li>PMP Certified</li>
<li>Green Belt Certified</li>
<li>Level 6 Coaching Cert.</li>
</ul>

Aidan McNabola

About Todd
With over 25 years of engineering and manufacturing leadership, Todd Johnson has consistently delivered operational excellence across complex, large-scale environments. He has provided direct and indirect oversight of teams exceeding 3,000 employees and has managed multi-plant operations with a focus on efficiency, compliance and strategic growth. His expertise spans corporate governance, including remediation efforts, regulatory compliance and successful navigation of inspections. Todd has led greenfield operations from initial startup through acquisition and has overseen capital projects ranging from $75,000 to $750 million, demonstrating a strong track record in project execution and organizational transformation.
Todd&rsquo;s leadership has been instrumental in several high-impact roles throughout his career. As VP of Engineering and Operations at Point BioPharma, he led the startup of manufacturing operations, including technology transfer, product development and compliance with government regulatory requirements. His specialized expertise in radioligand therapies played a key role in the successful transition of business and operations to Eli Lilly. Todd also managed investor and client expectations, ensuring project delivery and securing necessary funding. At Zimmer Biomet, he served as Director of Engineering and Operations, overseeing highly customized medical device manufacturing. He implemented inventory controls, enhanced quality record management and led a full overhaul of the quality systems. As Director of Engineering and Operations at Pharmedium, Todd focused on multi-site process standardization, led cleanroom expansions for continuous line operations and optimized cycle times in batch manufacturing environments. At Baxter, he held the role of Senior Director of Engineering and Operations, where he drove continuous improvement initiatives to enhance OEE, managed large-scale CAPEX projects, led S&amp;OP processes and oversaw new product introductions. He also played a pivotal role in the acquisition and integration of an aseptic filling/API facility in India. Early in his career at Abbott Laboratories, Todd served as Maintenance Manager, where he was deeply involved in navigating a consent decree and implementing corrective and preventive actions (CAPA), DMAIC, Six Sigma and Lean methodologies to support long-term compliance and performance improvement.
Todd holds a Bachelor of Science in Electrical Systems from Southern Illinois University and is a certified Six Sigma Green Belt.

Todd Johnson

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

Owen Clancy

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>

Health & Safety Officer

Karl Lippett

Health & Safety Officer

Quality Manager

Senior Quality Assurance Engineer

Process Development Engineer

Validation Engineer

Apply for this job