Electrician North West Ireland €50k+van With the successful acquisition of new contracts, our client is looking for experienced and self-motivated Electricians to join their team to carry out our repairs, testing & inspection, fault finding and new project work. Applicants should have relevant Electrician and Electrical Testing qualifications and be conversant in the servicing and installation of electrical systems. You will be expected to: * Electrical Installations on a variety of sites within the Water industry * Carrying out all electrical maintenance, servicing, and repairs * Carry out surveys and installations * Work on your own using your own initiative as well as alongside the existing team * Ensure tasks are completed with the appropriate H&S awareness. Requirements * Minimum of 3 years working in a similar role * Relevant Electrical certifications * Proven experience in electrical testing and inspections, and hold a valid QC Number * Safe pass & Manual handling certified * Full driving license * Ability to work autonomously For more information please contact Steve on (phone number removed). INFORM3 Recruitment is an equal opportunities employer. By applying to this position, you accept the terms of our privacy policy, please find this on our website

Team Horizon is seeking a Supply Chain Planner for our client who are a global biopharmaceutical company, for their site in Sligo. This person will play a crucial role in optimizing and managing the flow of products and materials throughout the site. The Supply Chain Planner will ensure all customer demand is fully met for new and existing products, through demand management, efficient production planning and inventory management. The successful candidate will ensure product availability through effective management of available capacity while maintaining cost and quality compliance. Why you should apply: * This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses. * There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives. * Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally. What you will be doing: * Develop and execute the supply chain strategy to optimize inventory levels, minimize stockouts, and reduce lead times. * Develop and maintain accurate demand forecasts and inventory plans to meet customer demand. * Collaborate with cross-functional teams, including procurement, manufacturing, logistics, and sales to ensure timely delivery of products and services to customers. * Monitor and analyze supply chain performance metrics, identify opportunities for improvement, and implement corrective actions as necessary. * Identify and assess supply chain risks, develop mitigation strategies, and implement contingency plans to manage disruptions. * Manage relationships with purchasing and suppliers to ensure timely delivery of materials and services and resolve any issues that may arise. * Maintain accurate and up-to-date records of inventory levels, procurement costs, and supplier performance. * Develop and maintain effective communication channels with internal and external stakeholders to ensure alignment of goals and objectives. * Participate in cross-functional projects to support business goals and objectives. * Any other duties assigned. What you need to apply: * Minimum 3 years’ experience in supply chain planning and execution. * Bachelor’s Degree or equivalent in an appropriate Technical or Business Discipline. * APICS (Desirable) Understanding & experience using MRP/ERP systems, especially SAP

Description Team Horizon is seeking a Process Scientist for our client in Sligo. This position is on 12-month fixed term basis. You will be part of a pilot plant project team and will provide technical support and program management to all relevant functional departments and NPI’s throughout the site. Your technical support will apply to all manufacturing operations from a chemistry perspective, and will develop new and innovative processes to deliver cost reductions. Why you should apply: * This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses. * There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives. * Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally. What you will be doing: * Execution of process development on existing products or new late stage clinical products including scale up to plant equipment. * Provide on-the-floor technical support to the Production Team Leaders for process/equipment optimization and troubleshooting. * Provide technical support to all manufacturing and chemistry related issues. Tasks include, daily trouble shooting, optimisation, cost reduction, training and coaching of manufacturing personnel. * Planning and leadership of technical transfers for future product introductions. * Identification and laboratory development of continuous improvement projects. * Work closely with process engineers and other departments to deliver these continuous improvement projects * Process and equipment optimisation in order to sustain and improve process chemistry, cleaning, product quality, yields and throughput. * Making recommendations and implementing measures to improve production systems, equipment performance, efficiency and quality of product. * Support of process front runs / use tests for both NPI and commercial processes. * Development of process control recipes for NPIs and optimization of existing commercial process recipes * Provide engineering support to all manufacturing and digital control system related issues. * Tasks include, daily trouble shooting, optimization, training and coaching of manufacturing personnel. * Support of all commissioning and validation activities during project start-up. * Development and update of batch and cleaning documentation for NPIs * Preparation of feasibility studies and operating budgets for future product introductions. * Identification and process development of continuous improvement initiatives to drive the required departmental cost reductions. * Coaching and training of all manufacturing personnel on technical/ chemistry elements of department operations Maintains regular contact with the other departmental team leaders and management, to ensure all site operations are operating effectively. * Adheres to and supports all EHS&E standards, procedures and policies

Role To coordinate the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements. Co-ordination, implementation and active participation in the site Validation Program. Responsibilities: * Ensure all Computerized systems are qualified in compliance with Data Integrity policies and regulatory requirements. * Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, * European cGMP and GAMP standards. * Generation/maintenance of the Validation Master Plans. * Generation/maintenance of Project Validation Plans. * Generation of validation plans, protocols and final reports to cGMP standard. * Review / approval of all protocols and final reports. * Management of validation change control process. * Adheres to and supports all EHS & E standards, procedures and policies Supervision Received * Individual is given authority to carry out their duties without close supervision. * Reports to Validation Team Leader. * Goals are reviewed on a regular basis and formal performance reviews are carried out once per year. Supervision Provided * No direct reports. * Provide guidance to functional areas the area of Validation. * May provide cross training and guidance to new department members. Qualifications: * 3rd level qualification in a relevant engineering or scientific discipline. Job/Technical Skills * A minimum of 5-10 years’ experience in a cGMP regulated environment. * A good understanding of regulatory requirements. Ownership and Accountability * The position has a high level of autonomy and individuals are expected to work on their own initiative. * Adheres to and follows all procedures policies and guidelines ensuring compliance with cGMP and HPRA/FDA regulations and company policies, procedures and guidelines. * Individual is fully responsible for the co-ordination and closure of projects assigned. * This position is crucial in identifying systems requiring validation and ensuring that this activity is documented, actioned and resolved. * This position impacts on product quality and technical performance as well as manufacturing operations. * Requires an ethos of Right First Time at all times. Decision Making/Impact * Expected to provide functional expertise to support daily operations. * Seeks Managers input when making decisions which affect the area. * Is a site SME on validation issues and provides guidance on same. * Decision making within confines of agreed responsibility with Team Leader. For immediate consideration please forward your CV to

Team Horizon is seeking a Validation Engineer on a permanent basis for our client’s manufacturing facility in the Northwest. Why you should apply: * You will get the opportunity to coordinate, implement and actively participate in the site Validation Program and general Technical Operations activities * Attractive Salary & Benefits Package on offer – Bonus, Healthcare,Pension as well as excellent career progression opportunities What you will be doing: * Coordination / direction and active participation in the validation of site Facility, equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards. * Generation/maintenance/execution of the Site Validation Master Plan, Project Validation Plans and schedules * Generation of validation protocols and final reports to cGMP standards. * Generation of validation investigations and implementation of corrective actions. * Creation, review and approval of various quality documents and test data. * Management of validation exception events and change control processes. * Maintenance and tracking of validation equipment, if applicable. * Performing cross training within the team and training of new team members. * Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems. * Communicating with peers and management regarding activities in the area, including elevation of events or concerns. What you need to apply: * Qualification and/or degree in engineering or scientific discipline. * 3 years plus validation experience in pharmaceutical, diagnostics or medical device industry & knowledge of cGMP and regulatory requirements * Strong communication (written and oral), presentation and troubleshooting skills required. * Effective interpersonal and organizational skills

Contract: 12 + Month Location: Sligo Responsibilities: * To provide Engineering services to the plant, in order to maximise the availability of all Site Process Equipment and Utilities. * To support the engineering teams in controlling uptime of process equipment and optimizing efficiencies both in equipment and process performance. * To support the Engineering team with the emphasis on continual operational improvements. * To provide process engineering support and technical trouble shooting within the site. * To improve the operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives. * To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining, troubleshooting and installing/commissioning equipment. * To provide engineering support and technical trouble shooting to all site operations and reliability of equipment and processes by the successful identification and implementation of continuous improvement initiatives. * Preparation of feasibility studies and budget management for all assigned projects. * Management and negotiation of external contracts and contractors. * Support all major site initiatives and sites core goals. ESSENTIAL Requirements * Degree in a relevant Engineering Discipline (Mechanical/Chemical/Process) * 5 years + strong site experience in API Manufacturing / OSD Manufacturing / BioPharm but will consider more junior (3 years) if they have relevant project site experience. * Proven track record in delivering Capital Projects – new equipment, utilities, facilities, etc. * Good knowledge of change control and C&Q processes/execution. Must have demonstrated relevant site experience of one or more of the below: * API process equipment trains (reactors, filter dryers, pumps, process pipework, milling, containment technology – gloveboxes, downflow booths, etc.). * Drug Product equipment (tablet press, roller compaction, tablet coater, material handling – post hoists, blenders, milling – Quadro Comils, etc.) * Cleanroom processing/utilities – HVAC, CIP systems, Purified water generation and distribution systems, etc. * Knowledgeable/competent with executing change control. * Experience in process engineering, with relevant experience of batch processing, automation, project management, commissioning and validation, equipment reliability and continuous improvement. * Working knowledge of distributed control systems, such as Delta V. * This is a hand-on role requiring a logical and structured approach to resolving day to day engineering issues typical of a live manufacturing environment. * Knowledge of cGMP and regulatory requirements relating to the Healthcare industry is required. * Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements. DESIRABLE * Trackwise change control system experience. * Electrical background – competency with electrical system design & installation (process equipment and site electrical infrastructure), familiar with ATEX regulations and requirements. For immediate consideration please forward your CV to

EHS Engineer Responsibilities * Ensure that the highest standards of Environmental Health and Safety are maintained throughout the plant in an ever-changing business environment. * Ensure compliance with all relevant EHS legislation and develop systems and procedures that optimizes the safety, health and environmental performance of the Site. * Ensure that effective contractor management systems and procedures are followed and maintain Contractor Safety Performance KPI’s. Requirements * BSc in Occupational Safety & Health Level 8, or equivalent, or a degree in a related discipline is a necessary requirement for this position * 2-3 years relevant experience Experience Required * Maintain ISO 14001 and ISO 45001 Certification. * Liaise with Managers /Ensure employees are trained to a defined competency standard with all applicable EHS policies and procedures. * Perform Risk assessments throughout the plant and oversee and monitor training on risk assessments. * Ensure adequate training is in place to ensure that employees and contractors can perform their roles in compliance with all EHS standards. * Support, improve and continuously monitor the Site Emergency Response Plan to ensure it meets the requirements of changing processes. * Support the Emergency Response Team during an EHS emergency. * Assist in induction and training of new and/or existing employees. * Auditing to ensure compliance with safety standards and with the corporate management and technical standards. * Monitor and achieve environmental targets such as recycling, waste, emissions etc. * Maintains and enforces the requirements of the sites environmental licence. For immediate consideration please forward CV to

Senior Automation Engineer Team Horizon is seeking a Senior Automation Engineer for a leading pharmaceutical company in Sligo. Why you should apply: * This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses. * There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives. * Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally. What you will be doing: * Manage Automation projects throughout the project lifecycle. * Provide technical support to all control system related issues. Tasks include, daily trouble shooting, optimisation, and documentation control. * Leadership of control system validation activities during project start-up. * Life cycle management of the on site control systems, to GAMP-4 requirements. * Project management of control system elements of continuous improvement projects. Work closely with process engineers/ technical support chemists and other departments to deliver these continuous improvement projects. * Project management and technical development of future integrations of the control systems, with planned MIS and ERP systems. * Departmental budgeting as delegated by the Automation & IT Manager. * Adheres to and supports all EHS & E standards, procedures and policies. * To administer and support all Automation & IT Processes in Pharmaceutical Manufacturing environment. * Implement, qualify, commission and maintain manufacturing Automation & IT systems (MES, SCADA) and associate IT infrastructure that delivers operational efficiency and agility. * Identify, evaluate and implement opportunities for continuous Automation & IT process improvement. * Define requirements on capital projects and interact with internal & external stakeholders, vendors and contractors. * Work with Production/Engineering and Quality to troubleshoot and optimise output, minimise contamination and minimise costs. * Generate & Maintain documentation (SOP’s & Technical Documentation) for full cGMP validation and operation, including documentation of changes made. * Maintain Data Integrity Program, including remediation of legacy systems to ensure robust procedure and systems are in place covering data integrity, security and recovery. * Actively Contribute to the Automation Business Strategy. * Any other duties as assigned. What you need to apply: * Relevant 3rd level degree in Mechatronics, Electronics or Computer Technology. * 5-10 years’ experience in process automation, with relevant experience of batch processing and DCS platforms in a GMP environment in the pharmaceutical industry. * 3 years’ experience of the 21 CFR Part 11 requirements for automated systems in the pharmaceutical industry. * 3 years plus of Experience of plant start-ups and/or new product introductions to pharmaceutical facilities. Must be able to lead these activities in a start-up environment. * Experience with PLC (Siemens), SCADA and process equipment. SCADA experience (iFix, WinCC). Knowledge of Shop floor Network & Control Architecture with Electronic Batch Record Implementation. Instrumentation/Automation & Control knowledge with BMS / SCADA / DCS / PLC

Senior Project Engineers - Biologics Process Equipment Team Horizon is seeking a Senior Project Engineers - Biologics Process Equipment for a leading pharmaceutical company in Sligo. Why you should apply: * Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work. * You will join an innovative team, working among a diverse group of visionaries, thinkers and doers, working on developing pioneering solutions that lead to shared success. * You enjoy working in a culture of learning and collaboration and making a positive impact. What you will be doing: * Safely coordinate and lead cross functional project teams for the delivery of processing equipment to the site based on planned timelines and scope. * Processing equipment would include e.g., Autoclaves, RABS & Isolator Filling machines, LAF units, Compounding skids, Vessels, Containment booths & Stopper processing eq. * Writing User Requirement Specifications. * Selecting Vendors and completing Vendor evaluation matrix. * Writing RCE's, placing orders, Project Management & Design review meetings. * Working to the ASME BPE 2019 Standard and relevant ISPE Guidelines etc. * Coordination of processing equipment installation and services hook up, working with Equipment Vendors and Engineering personnel. * Lead the Project Team participation in Factory Acceptance Testing program. * Coordination of all equipment documentation requirements. * Commissioning of equipment and Engineering support during qualification. * Work with the E&T Senior Manager & System Owner / Project Team. * Handover training, coordination of O&M manuals, Spare parts, & PM schedules. * Contribute to a team environment on specific technical problem-solving forums associated with Product manufacture & Aseptic fill. * Deliver on Process improvement / cost reduction projects. * Lead your regular weekly / bi-weekly Project review meetings with your Project team. * Attend the weekly Tier 1 meeting with your manager. * Liaise with Senior Engineering Manager, Equipment Vendor, Quality Leads, Validation Engineers, Operation Leads, Technology Leads, Maintenance technicians and Business Technology Technicians. * All other duties as requested or assigned. What you need to apply: * Third level qualification in an Engineering or equivalent discipline/experience. * Experience of working in Biologics, Pharmaceuticals or Medical device industry. * Minimum of 2 to 5 years’ experience. Project Management experience with a proven record. * Assured self-starter with proven technical ability. * Good communication and Interpersonal skills required to operate in a multi-function project team set up. * Ability to work within a team using your own initiative to articulate and deliver specific functional requirements for all aspects of the project and work with members of various disciplines and functions across the project. * Good team leading skills and ability to work closely with other areas/departments within an organization. * Experience in commissioning and cycle development/Validation/startup would be a huge advantage

Live the cabin crew life! Join our team as Emirates cabin crew and see the world as you work. This is your opportunity to be part of the world’s largest international airline. Look forward to a tax-free salary, free accommodation and great travel perks for you and your family. Make Dubai your home and enjoy all the benefits of this vibrant city. If you’re ready for a career that takes you places, apply online now and start your adventure with Emirates. Starting Salary & Flying Pay Your pay is made up of three components: a fixed basic salary, an hourly pay for operated flights and an overseas meal allowance. Basic salary: AED 4,430 / month Flying Pay: AED 63.75 / hour based on avg. 80-100 hours / month Average Total Pay: AED 10,170 / month (~USD 2,770, EUR 2,710 or GBP 2,280) These are approximate numbers for Grade II (Economy Class). Hotel accommodation as well as transport to and from the airport is provided by the company. We are looking for: 1+ year of hospitality or customer service experience Positive attitude with the natural ability to provide excellent service in a team environment, dealing with people from many cultures High school graduate (Grade 12) Fluency in written and spoken English (ability to speak another language is an advantage) Arm reach of 212 cm while standing on tiptoes and minimum height of 160 cm which will enable you to reach emergency equipment on all aircraft types No visible tattoos while you’re in Emirates cabin crew uniform (cosmetic and bandage coverings are not allowed) Can adapt to new people, new places and new situations As Emirates cabin crew, you will be based in Dubai and will need to meet the UAE’s employment visa requirements Fly Emirates. Fly Better.