1 week ago Be among the first 25 applicants Direct message the job poster from Elusav Recruitment Technical Recruitment Specialist - Industrial Recruitment - Data Centers - Pharmaceutical - SemiConductor - Qualified Engineer (BEng,MSc) Elusav Recruitment have an amazing opportunity for Technical Sales Engineer - Heat Pumps to join exciting and market-leading specialist in Renewable Energy Sector in Offaly. As the Technical Sales Engineer you will be responsible for identifying and pursuing new business opportunities to meet and exceed sales targets. Responsibilities: Roll out CPD’s to Mechanical Consultants, specifiers, developers, County Councils, OPW, etc. Build and maintain strong relationships with consultants, contractors, and key stakeholders. Develop and implement strategic plans to increase market share within the sector. Manage inventory & forecasting. Conduct market research and competitor analysis to identify trends and opportunities. Prepare and deliver compelling sales presentations and proposals. Take ownership of projects from specification & quotation to final installation. Collaborate with internal teams to ensure client satisfaction and project success. Report on sales performance and provide insights on market developments. Requirements: 3+ years of business development experience, ideally in construction sales. Proven track record of achieving and exceeding sales targets. Ability to work independently and manage time effectively. Knowledge of commercial heat pumps would be an advantage. Contact: If you would like to learn more about the vacancy, apply now, or contact Brendan Mullins on +353 61 527 150 or Bmullins@elusav.com Seniority level Associate Employment type Full-time Job function Industries: Construction and Engineering Services #J-18808-Ljbffr
Elusav Recruitment have an exciting opportunity for an EPlan Design Engineer to join a prominent engineering contractor specializing in wastewater and water treatment in Limerick/North Cork. As the Design Engineer you will be responsible for designing and drafting various types of control panels, including Form 2 to Form 4, in accordance with project requirements and client specifications. Responsibilities: Possess a strong understanding of industry standards, including IEC-60439 and IS-10101. Proficiently create schematics for a range of components, including ATS, DOL starters, intelligent MCCs, VSD starters, and PLCs. Prepare Bill of Quantities (BOQ) and part lists based on drawings and collaborate with vendors for procurement. Generate detailed loop drawings to facilitate field installation and equipment interconnection. Utilize E-plan/Pro-panel software for drafting and design tasks. Collaborate effectively with a multidisciplinary design team. Contribute to the growth and success of an organization with operations in Ireland, the UK, and North America. Ensure compliance with electrical trade qualifications. Requirements: Minimum of 3 years' experience as an electrical control panel draftsperson with expertise in E-plan/Pro-panel. Electrical trade qualification is required. Contact: If you would like to learn more about the vacancy, apply now, or contact Thaissa Torres on Ttorres@elusav.com or +35315822807. Seniority level Mid-Senior level Employment type Full-time Job function Design, Engineering, and Information Technology Industries Construction and Design Services #J-18808-Ljbffr
Elusav Recruitment have an exciting opportunity for a Preconstruction Project Manager to join one of the most reputable Engineering Contractors in Dublin. As the Preconstruction PM you will be fully accountable for the bid proposals submitted to the clients and being the single point of contact for the clients and to present the company proposal to internal stake holders and the client. Responsibilities: Review the project documentation and set up a project execution plan for the proposal. Manage estimating, preconstruction and business unit resources dedicated to the bid project. Prepare and hold presentations for the internal project review. Prepare and hold presentations for client meetings. Engage with designers for proposals on detailed design development. Engage with the delivery business unit to identify a team for the project. Review tender deliverables and develop responses to all tender deliverables. Review and ensure that project information is shared to the team in accordance with the internal procedures. Drive a critical review of the project and table alternative proposals for a better delivery of the project. Review the construction methodology to identify programme implications and any necessary temporary works. Develop the project schedule of works in cooperation with the project team. Plan out the logistics of the project and develop a draft logistics plan. Engage with supply chain to identify possible supply chain partners for the specific projects. Review project responsibility matrix to clarify the scope for the bidding subcontractors. Review subcontract proposals and review technical / commercial comparison for evaluation and selection of preferred bidder. Review project control sheet and the estimate together with bid manager and estimators. Review requirements for lifting and cranes and develop a crane strategy for the project. Identify project risks and mitigation plans to deal with these risks. Other items and deliverables specific to each project. Requirements: Third level degree in and Engineering subject (Mechanical, Electrical, Construction or similar). 5-10 years experience, including 5 as a Project Manager. Experience in Preconstruction Project Management. Project Management experience. Contact: If you would like to learn more about the vacancy, apply now, or contact Aaron Gallagher on Aaron@elusav.com or +35361541446. #J-18808-Ljbffr
Elusav Recruitment are delighted to offer an outstanding opportunity for a MEP Contracts Manager with one of Ireland’s most respected and long-established construction companies based in Dublin. This is a fantastic opportunity to manage multiple large scale high density residential & commercial projects, drive modern methods of construction with focus on quality & safety from the start. There’s also clear scope for progression within a well structured and forward thinking business who, under the leadership of a credible MEP Director, have doubled in size their MEP Division & have restructured MEP offering & delivery with serious ambition to become progressive leader in this sector. Responsibilities: Manage multiple projects simultaneously. Champion modern construction techniques. Ensure the highest standards of safety and quality. Start with the end in mind and drive project success. Responsible for the management of multiple projects concurrently at any one time. Responsible for contracts and ongoing relationships with suppliers. Co-ordinate and supervision of all the MEP activities. Ensure all operations are performed effectively and efficiently in accordance with the company’s construction program. Ensure all work is carried out in a safe, proper and thorough manner taking into account H&S legislation, company policies and procedures, risk assessments and method statements. Requirements: Proven experience leading MEP Operations, ideally 8+ years. High Density Residential experience preferred. Trade or Degree qualified in Mechanical or Electrical discipline. Must be flexible to travel to site as required. Contact: If you would like to learn more about this vacancy, apply now or contact Aaron Gallagher at Aaron@elusav.com or +35361541446. #J-18808-Ljbffr
Elusav Recruitment have an amazing opportunity for a CQV Engineer with a leading global biopharma company in Waterford, Ireland. As the CQV Engineer, you will be required to support new product introductions, equipment qualification and the site requalification program. Responsibilities: Designing, executing and reporting on PV/Process Performance Qualifications. Designing, executing and reporting on validation studies for equipment, systems and processes. Ensuring validation studies are managed in conjunction with all required standards and legal requirements (Health & Safety, cGMP, construction, environmental etc.). Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation and depyrogenation. Ensuring that the validation status of equipment and systems are in compliance with cGMP at all times. Maintaining validation documentation through the validation lifecycle. Participation in external regulatory inspections. Support Site Change Control process. Requirements: 3-5 years’ experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector. Degree in Science (Chemistry, Micro. or Pharmacy preferred) or Engineering Chemical/Mech/Elec). Capable of troubleshooting validation issues associated with projects, process development etc. Competent technical knowledge of pharmaceutical plants. Previous validation/product development experience would be highly advantageous for the role. Knowledge of Process Validation regulations, current process validation and technical transfer industry practices, and experience of interpretation and application of guidelines and regulations. Knowledge of requirements for GAMP, ISPE Baseline guides. Knowledge of steam and dry heat validation publications such as AAMI/ANSI, PDA and ISO guidelines. Full understanding of relevant quality and compliance regulations. Able to execute projects to plan. Good knowledge of quality management systems. Good communication skills at organisation, team and individual levels. Ability to use MS Project and SPC packages an advantage. Understands KPI’s for the site. Contact: If you would like to learn more about the vacancy, apply now, or contact Stephen O'Brien on Stephen@elusav.com or +3536959993. Seniority level Associate Employment type Contract Job function Engineering, Science, and Project Management Industries Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Chemical Manufacturing #J-18808-Ljbffr
Elusav Recruitment have an exciting opportunity with a leading global Pharma and Biopharma company who is seeking a Production Operator to bring value to their facility in Dublin. The role consists in undertaking manufacturing operations involved in the production of biologic drug substance on their designated shift. Responsibilities: Work with the manufacturing operations group, project design team, the CQV team, the Automation/CSV reps to facilitate the development and validation of the manufacturing facility. Support Equipment Design/ HAZOP and Room programming reviews. Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g., EHS metrics, Production Plan, OEE, compliance and team training. Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures. Generate SOPs/Electronic Batch Records. Adhere to Right First-Time principles. Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested. Escalate issues as appropriate to Process Lead. Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan. Requirements: Minimum of a Level 7 qualification in a science or engineering discipline, or a Level 6 with a minimum of 2 years’ experience in a GMP Manufacturing requirement. Knowledge of applying Lean Six Sigma and Lean methodologies in a workplace environment. Experience in a highly regulated pharmaceutical manufacturing environment is desirable. Start-up experience in a large-scale commercial drug substance facility desirable but not essential. Good understanding of Upstream/Downstream Processing and experience an advantage. Contact: If you would like to learn more about the vacancy, apply now, or contact Thaissa Torres. #J-18808-Ljbffr
Elusav recruitment have an exciting opportunity for a Senior Buyer with a leading Global Biopharmaceutical in Cork, Ireland. The Senior Buyer will play a lead role in the co-ordination and execution of all activities related (but not limited) to the planning and purchase of components by converting the output of the Master Schedule and detailed schedule (MRP) for production needs into material requirements to ensure availability of the right quantity when needed. Responsibilities: Develop & Execute the Materials Requirement Plan (MRP) by ensuring efficient and effective procurement & inventory practices and optimizing the balance between quality, service, reliability and cost to ensure that patient / customer requirements are met while maintaining compliance. Ensure a key focus on master data of materials in SAP to ensure correct signals are received in a timely manner. Ensure that all material delivery schedules are communicated to the suppliers on time in order to meet planned requirements. Maintain raw material and consumable inventories within target, while minimizing excess, obsolete and expired materials. A strong self-starter who uses initiative to identify, communicate and resolve issues as they arise. Communicate when required at the site “Run the business” meetings, any potential impacts to the production schedule, supplier reliability/service issues. Escalate as appropriate through site and global forums to ensure issues/criticalities are resolved in a timely fashion. Interface with Quality and Warehouse staff regarding any rejected / defective materials, making the necessary physical arrangements with the supplier through GSQ to ensure a prompt return of goods or disposal. Support Scenario planning (RCCP) when required with colleagues in the Material Operations, planning function, by performing material feasibility analysis. Liaise with suppliers to clarify potential plan constraints and interfaces between supplier and the key internal stakeholders to ensure issue resolution. Support operational readiness activities where required. In collaboration with Tops Global Procurement (TGP), manage the supplier and materials selection process with supplier agreements where applicable. In collaboration with TGP, ensure the new material qualification process is managed and new materials created and set-up sufficiently on SAP to ensure accurate and efficient planning and purchasing. Partner with TGP to drive supplier performance improvement, including quality and on-time delivery in line with production schedule. Track and report site level supplier service performance, communicating the information to the relevant parties where relevant. Execute potential deviations to the plan assessing with the supplier the feasibility of such changes, rapidly highlighting to the affected internal stakeholders if the changes are not possible from a materials/consumable’s perspective. Liaise with warehouse to understand and adhere to space constraints, managing inventory levels within agreed targets. Effectively partner with all internal and external business partners, while also leading and influencing cross functional teams to ensure the best possible solution to problems. Focus on and encourage continuous improvements (CI) of the process being supported (e.g. MRP signal improvement initiative). Develop and project manage local and global programs to deliver continuous improvement in KPI’s including Customer Service, Inventory and Cost. Align with strategies and realization of departmental and business goals. Co-ordination and completion of required compliance process activities including Change Control, Deviations, Event’s & CAPA’s. Requirements: A minimum of an Honour’s Degree (NFQ level 8) in Supply Chain Management or other related Business discipline is essential. Supply Chain Certification is preferred e.g. APICS. Project Management or Lean Certification is desirable. A minimum of 5 years relevant Supply Chain Management experience. Experience in Planning/Purchasing in a pharmaceutical environment with strong technical/systems background is desirable. Experience of SAP would be beneficial, but ERP system competency is essential. Prove track record in managing a direct material category. Power BI or similar data analytics visual tool knowledge is desirable but not essential. Experience working in a GMP environment. Contact: If you would like to learn more about the vacancy, apply now, or contact Brendan Mullins on +353 61 527 150 or Bmullins@elusav.com #J-18808-Ljbffr
Elusav Recruitment are currently recruiting for a Production Manager to join a highly reputable OEM Manufacturer that manufactures and fabricates bespoke Pressure Vessels and Process Skids. Equipment predominantly for Pharma, Biopharma and Food and Beverage industries. Responsibilities: Site Senior Management Team (SMT): Be an active member of the Site SMT, contributing to strategic planning and decision-making processes. Resource Management: Manage workshop resources effectively to ensure delivery dates are met in line with customer expectations and within budget. Responsible for ensuring adherence to all KPI's (Safety, Quality, Service, Cost, and People Development). Quality Assurance: Ensure that all projects are delivered in accordance with approved drawings, standards, weld procedures, and customer expectations. Foster a customer-focused approach among all staff, emphasizing the importance of quality in every aspect of the production process. Continuous Improvement: Promote and further develop a culture of continuous improvement across the production team and lead initiatives aimed at enhancing efficiency, quality, and safety in production processes. Health & Safety Compliance: Ensure compliance with all Health & Safety regulations and drive improvements in safety culture and performance. Conduct regular safety audits and training to maintain a safe working environment. Team Leadership: Lead, mentor, and inspire the production team to achieve goals and maintain high levels of performance. Champion a positive employee environment by promoting open communication, engagement, and team development. Promote a culture of inclusiveness, trust, flexibility, and teamwork. Ensure effective processes in the selection of competent talent and support the development of future potential experts and leaders. Ensure effective training and performance management processes are in place and executed. Scheduling: Develop and refine scheduling processes to ensure quick and accurate updates on production timelines and resource allocation. Ensure that the necessary capacity is in place across the workshop to meet customers' demands. Capital Expenditure Management/Opex: Identify and submit CapEx/Opex requests to the Board/SMT for approval, identify future CapEx/Opex requirements and deliver projects that align with organizational goals. Environmental: Ensure that workshops contribute towards the organization’s environmental goals and objectives and collaborate with teams to implement sustainable practices in production. Facilities: Oversee the upgrade and upkeep of the facility to maintain world-class standards. Manage the upkeep and servicing of all facilities, equipment, and machinery in the workshops. Requirements: Bachelor’s degree in Mechanical, Production, Manufacturing Engineering, or a related field. Proven experience (5+ years) in operational/manufacturing leadership roles within the engineering or related industry. Proficiency in project management and process optimization, with a strong focus on meeting deadlines. Familiarity with relevant regulations and compliance requirements in the manufacturing sector. Ability to manage budgets effectively and ensure resource allocation aligns with organizational goals. Experience with continuous improvement methodologies and a track record of implementing successful initiatives. Proven experience in implementing Lean and Six Sigma methodologies to optimize production processes and enhance operational efficiency. Strong background in developing and managing production schedules to ensure timely delivery while optimizing resource utilization. Contact: If you would like to learn more about the vacancy, apply now, or contact Brendan Mullins at Bmullins@elusav.com or 061527150. #J-18808-Ljbffr
Elusav Recruitment have an amazing opportunity for a Head of Sterility Assurance and Microbiology with a leading global biopharma company in Waterford, Ireland. As the Head of Sterility Assurance and Microbiology you will be responsible for developing and implementing effective strategies and procedures for sterility assurance and microbiology across the organization. Responsibilities: Develop and implement comprehensive sterility assurance and microbiological programs in alignment with the organizational strategy, vision, and objectives. Ensure the compliance of products and processes with applicable sterility assurance and microbiology regulatory requirements and company quality standards. Maintain a system to ensure sterility assurance and microbiological risks are properly identified, tracked and mitigated. Oversee, with Q&V team, the validation, qualification and monitoring of methods, equipment and the environment ensuring sterility assurance control. Follow metrics and monitor data for the sterility assurance and microbiological activities, to identify trends and issues and to implement action plan. Promote a culture of quality throughout the organization, identifying and driving continuous improvement initiatives and projects to enhance the sterility assurance and microbiological activities. Evaluate and recommend new technologies, tools, and methods to enhance sterility assurance and microbiology. Lead management reviews to assess the effectiveness of the sterility assurance program and microbiological program. Lead and manage the sterility assurance and microbiology team, including hiring, training, coaching, professional development and performance evaluation. Interact with external bodies & Global Quality to bring knowledge and awareness of best industry practices. Prepare and participate in regulatory inspections and audits, providing expertise on sterility assurance and microbiology. Requirements: Degree and/or Master’s in a science or engineering discipline. Over 7 years of experience in the Pharma industry, with at least 4 years in a leadership role within aseptic/sterile manufacturing or Microbiology. Proven experience in microbiology and sterile manufacturing. Strong leadership and experience in developing and mentoring technical teams. Expertise in aseptic manufacturing, regulatory requirements and product technical transfer. Strong communication, decision-making, and analytical skills. Proficient in Lean Principles and process control strategies to enhance operational effectiveness. Contact: If you would like to learn more about the vacancy, apply now, or contact Brendan Mullins on +353 61 527 150 or Bmullins@elusav.com #J-18808-Ljbffr
As the Qualified Person you will be responsible for ensuring that practices at the company are in compliance with cGMP as stated in Directive 2003/94/EC and in the Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2002. Responsibilities: Ensure practices and products released from the site are in compliance with cGMP as stated in Directive 2003/94/EC and in the Rules and Guidance for Pharmaceutical manufacturers and Distributors 2002. Provide oversight and support improvement of site quality systems and GMP practices. Review and approval of Quality documentation. Work with relevant departments to ensure timely closure of quality actions/ findings. Support investigation of deviations ensuring all product deviations are closed prior to product release. Complete all duties as per relevant local and global procedures. Conduct duties in a safe manner and report all safety issues or concerns. Maintain work area to good housekeeping standards. Lead quality improvement projects. Mentor QA Specialists. Actively contribute to continuous improvement initiatives. Requirements: Third level qualifications (degree in science or related discipline preferred) appropriate for eligibility for Qualified Person status. Minimum of 5 years’ experience in the pharmaceutical industry in a QA role. Contact: If you would like to learn more about the vacancy, apply now, or contact Stephen O'Brien at Stephen@elusav.com or +3536959993. #J-18808-Ljbffr
