A leading pharmaceutical company is seeking a Maintenance Engineer for their site in Sligo, Ireland. This full-time on-site role requires maintaining machinery and ensuring compliance with GMP standards. Candidates should have at least 5 years of industry experience, particularly in maintenance within a GMP environment, and possess a Bachelor's degree in engineering. Additional skills in problem-solving and the ability to manage maintenance projects are essential. #J-18808-Ljbffr
•The Maintenance Engineer is an integral part of our Engineering team based out of our Ireland - Sligo site. •This role is full-time on-site in our Sligo site. The weekly working hours are Monday to Friday 8:30am to 17:00pm. Key Responsibilities Maintain machinery, plant, equipment, utilities, facilities and services to required operating standards, ensuring that the validated state of GMP equipment is maintained. Perform installation, emergency, corrective and preventive maintenance of equipment. Perform routine PMs and related paperwork according to scheduled timelines and ensure that eMaint (CMMS) is updated. Coordinate and manage maintenance contractors/equipment vendors on site, issuing and control of permits to work. In partnership with Operations, Quality and TSA troubleshoot issues, providing engineering expertise to find solutions promptly. Perform duties in a compliant manner and in accordance with all site SOP’s, EHS standards and guidelines and relevant legal requirements. Breakdown analysis. Work closely with project team to assist in the specification, installation, commissioning and testing of new or recommissioned equipment/plant/utilities. Attend FATs to ensure adherence to user requirements specifications and associated requirements. Own or provide engineering input to deviations, CAPAs and change controls. Participate in internal audits. Deal with any problems or issues escalated from Operations which may affect production. Management of inventory. Participate in projects to improve system performance and reliability. Assist in developing and implementing line/process improvements to achieve required OEE, support continuous improvements. Provide ‘On Call’ support for the site. Escalate issues with equipment or its management to the Engineering Manager. Perform other duties as assigned. Essential Education and Experience Bachelor degree or similar trade qualification in an engineering discipline 5 years+ of industry experience in a GMP manufacturer with at least 3 years’ experience in maintenance of chemical, HVAC/mechanical systems, pneumatic & hydraulic system, electrical power systems, control systems, building management systems Experience in maintaining utilities, facilities & production/process equipment Good team player who enjoys collaboration. Proactive attitude with ability to work on own initiative within the Phibro Quality Management and Engineering Standards framework. Understanding of the different level of work order priorities. High level of accuracy and attention to detail. Appreciation of total cost of ownership in dealing with equipment specification, repairs and maintenance. Analytical skills and ability to problem solve. Understanding of the relevant quality standards. Sense of ownership and accountability for own work. Experience of participating in project work and handling multiple tasks. Proficient in written and spoken English. Proficient in MS packages. Predictive maintenance regimes and routines Experience working with CMMS (Computerized Maintenance Management Systems) – eMaint an advantage. Time management. Desired Education and Experience Experience in tablet manufacturing or other pharmaceutical areas. AHU’s, Autoclaves and Lyo experience would be a strong advantage. Experience with utilities (black and clean utilities) Equipment validation experience. Experience with AutoCAD and ability to read & interpret technical drawings & specifications Phibro is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. Business Unit: Animal Health & Mineral Nutrition Division: Animal Health & Nutrition Department: Engineering Location: Ireland - Sligo Work Schedule: Monday - Friday (40 Hours) #J-18808-Ljbffr
About Phibro Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,300 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. The Graduate Engineer is an integral part of our Engineering team based out of our Ireland - Sligo site. We are seeking a motivated and detail-oriented Graduate Engineer to join our team at a EU GMP compliant vaccine manufacturing facility. This is an exciting opportunity to be involved in validation, qualification, and routine support of critical equipment and cleanroom environments. Key Responsibilities Temperature Mapping and Environmental Monitoring: Plan, execute, and document temperature mapping studies for storage areas (cold rooms, freezers, incubators, warehouses) and critical process equipment. Perform risk assessments to define mapping strategy and sensor placement. Analyze data for compliance with EU GMP and internal quality standards. Generate and review validation protocols and reports (IQ/OQ/PQ). Autoclave Load Qualification: Support the qualification of autoclaves, including moist heat sterilization cycles. Develop and execute load patterns and thermal distribution/equilibration studies. Ensure Biological Indicators (BIs) and thermocouples are placed per GMP requirements. Analyze cycle performance data and support requalification activities. Equipment Qualification and Validation: Assist with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for new and existing equipment (e.g., HVAC, clean steam, washers, filling lines, isolators). Support validation life cycle documentation and change control processes. Collaborate with cross-functional teams (QA, Manufacturing, Maintenance). Cleanroom and Facility Support: Support routine cleanroom qualification (HEPA integrity testing, airflow visualization, pressure differential monitoring). Participate in periodic requalification and deviation investigations. Assist in maintaining the state of control of classified environments. Other duties as assigned. Documentation and Compliance Prepare and review engineering documentation in compliance with EU GMP Annex 15, EMA, and FDA standards. Completion of work orders in the engineering system Follow Good Documentation Practice (GDP) and support audit readiness. Contribute to continuous improvement initiatives and deviation/CAPA investigations. Essential Education and Experience Bachelor’s degree in Mechanical, Chemical, Biomedical, or Process Engineering (or equivalent). Strong interest in GMP-regulated pharmaceutical/biotech manufacturing. Familiarity with validation principles and GMP guidelines (e.g., Annex 15, ICH Q8/Q9/Q10). Proficient with Microsoft Office. Excellent attention to detail, analytical mindset, and willingness to learn. Strong written and verbal communication skills. Desirable Education and Experience Internship or co-op in a regulated manufacturing or laboratory setting. Experience with GxP documentation or working in a cleanroom environment. Basic understanding of equipment like autoclaves, clean steam systems, HVAC systems, and temperature control devices. To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits. Phibro is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. Business Unit: Animal Health & Mineral Nutrition Division: Animal Health & Nutrition Department: Engineering Location: Ireland - Sligo Work Schedule: Monday - Friday (40 Hours) #J-18808-Ljbffr
Select how often (in days) to receive an alert: About Phibro Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,300 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. Responsibilities Lead & develop the Engineering team across Maintenance, Utilities, Calibration, Revalidation, Computer System Validation, Automation, Building Management Systems, & Capital Projects. Provide strategic oversight of all engineering activities, ensuring alignment with site goals and regulatory requirements. Oversee all capital projects on site. Maximise production & utility equipment reliability through planned maintenance execution, incident investigation, root cause analysis, & CAPA implementation. Oversee engineering aspects of facility qualification, equipment commissioning, & validation. Ensure engineering systems & processes meet EU GMP, EHS, & corporate standards. Maintain the validated state of critical utilities & equipment, ensuring readiness for audits & inspections. Own the site maintenance strategy, including predictive & preventive programs, & ensure effective use of CMMS tools. Champion energy efficiency, sustainability, & continuous improvement initiatives. Manage the engineering department’s expense budget, including utilities, facilities, & repairs. Collaborate with EHS to ensure safe working conditions through risk assessments, inspections, & safety programs. Collaborate cross-functionally with Operations, QA, QC, TSA and EHS teams. Skilled in CAPA, deviation, & change control processes; responsible for providing engineering input to same. Support, participate & lead internal and external audits. Drive compliance to regulatory standards & be audit facing to bodies such as the HPRA. Foster a culture of accountability, innovation, & technical excellence across the engineering function. Ad hoc duties as assigned. Education Bachelor’s or Master’s degree in Mechanical, Electrical, Chemical, or Process Engineering (or related discipline). Experience Min 10 years of experience in pharmaceutical or biotech manufacturing, with at least 3 years in a senior leadership role. Proven experience in GMP-regulated environments; vaccine & sterility experience is an advantage. Deep understanding of engineering compliance, automation, calibration, & utility systems (e.g., WFI, HVAC, clean steam). Proficiency in CMMS systems & project management tools. Demonstrated success in leading cross-functional teams & managing external contractors/vendors. Excellent problem-solving, leadership, & communication skills. Leadership & Management Competencies Ability to motivate, guide, & develop a team of engineers. Excellent written & verbal communication skills to effectively convey information to both technical & non-technical audiences. Ability to delegate tasks effectively & empower team. Strong ability to build relationships with stakeholders. Ability to resolve conflicts & manage difficult situations effectively. Ability to contribute to the development of strategic plans & goals. Ability to analyze data, identify trends, & make informed decisions. Attention to detail is critical to ensure compliance & product quality. Ability to plan multiple & complex workstream activities. Ability to manage multiple priorities. To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits . Phibro is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. Business Unit:Animal Health & Mineral Nutrition Division:Animal Health & Nutrition Department:Engineering Location:Ireland - Sligo Work Schedule:Monday - Friday (40 Hours) #J-18808-Ljbffr
A leading animal health organization in Sligo is seeking a Senior Engineering Manager to lead the Engineering team and ensure compliance with industry standards. The ideal candidate will have over 10 years of experience in pharmaceutical or biotech manufacturing and a relevant degree. Responsibilities include managing engineering projects, fostering team development, and driving compliance efforts. Competitive benefits are offered. #J-18808-Ljbffr
