Within this role you will manage the QC Microbiology team and provide critical microbiology support to manufacturing and facilities. Applying for this role is straight forward Scroll down and click on Apply to be considered for this position. A typical day might include, but is not limited to, the following: Managing a team of laboratory analysts within the QC microbiology department involved in the analysis of raw materials, intermediates (in process) and bulk drug substance in a cGMP regulatory environment Implementing and managing the environmental monitoring programme, including surface, settling and viable and non-viable particulate air monitoring of aseptic operations and controlled areas Managing QC microbiological operations to ensure compliance with cGMP standards and accurate sample analysis Designing and overseeing microbiological validations as needed for drug substance, in-process controls and buffers Managing the design, validation and execution of the clean utilities qualification and re-qualification program Supporting manufacturing personnel in the identification of microbiological root cause analysis and provide technical advice on QC related topics as needed Participating in the investigation and review of alert and action limit investigations as needed and implements corrective action as appropriate Ensuring that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs) Reviewing and approving method protocols, reports and SOPs Assisting in the preparation for internal/customer/regulatory inspections Ensuring a safe working environment within the laboratory Overseeing or conducting laboratory investigations and generates reports in response to invalid assays, Deviations, OOS/OOT Ensuring that CAPAs and Change Controls are initiated and completed on time and in accordance with site procedures Presenting analytical data reports clearly and concisely to senior management, including QC performance metrics and trend This role might be for you if: You have the ability to train, develop and mentor direct reports and effectively manage the performance of individuals You can proactively identify and implement lab process improvements, lean initiatives To be considered for this opportunity you should have a BS/BA in Microbiology or closely related field with 6+ years' experience in microbiology lab, preferably in the pharmaceutical or biotech industry with 3+ years' experience in a leadership role in microbiology laboratory management. #REGNIRLTO Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit For other countries' specific benefits, please speak to your recruiter. Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron's roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron's on-site policy and expectations for your role and your location. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U. positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. xsokbrc Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. TLNT1_IJ

Overview Job title: Quality Controller Reporting To: Technical Manager Role Type: Full time, Permanent Location: Carrolls Cross, Co. Is this the next step in your career Find out if you are the right candidate by reading through the complete overview below. Waterford Closing Date: Role Summary: Dawn Meats are currently recruiting for a Quality Control Operative to join the Carrolls Cross Convenience Foods & Retail Quality Team. Working as part of the FSQ team to support the production team by ensuring that the quality of the product is tested and measured at regular daily intervals ensuring it meets all production, food safety, hygiene and customer specifications across the Convenience Foods and CX Retail production areas. Responsibilities Your role will see you tackle a wide range of business challenges in a busy quality and production environment. The successful Candidate will be responsible for: Work to an hourly schedule to complete quality and due diligence checks on product, to ensure that it meets required customer and legal specifications. Carry out pre-start checks in production areas daily. Record and regularly report product quality information and feedback to quality team lead and production team shift manager for quality improvement. Collection of meat and environmental samples for microbial testing. Assist in projects as outlined by the QC Team Leader, Quality Supervisor and/or FSQ Managers. QC decision making based on data collection and analysis. Aiding production staff where necessary regarding product safety, quality or traceability control procedures. To be involved with Customer & 3rd Party Audits. To ensure a culture of "Always Audit Ready" is implemented within the production area. Qualifications The ideal Candidate will have or demonstrate: Have good understanding of English. Good communicational skills. Team working skills. Have good problem-solving skills and be able to use own initiative. Keen attention to detail. Willingness to learn. Must be flexible and able to support QC team members. Be able to work a three-shift pattern and be available to work Saturdays when scheduled to do so. (Days Evenings Mid-Shift) Own transport is preferred. INDLP To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register. TLNT1_IJ

Overview PM Group is a leading international engineering, architecture, project and construction management firm. While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required. With a network of offices in Europe, Asia and the US and a multi-discipline team of over 3,700+ people, we deliver complex, capital projects in the life sciences, food and beverages, mission critical/ICT, advanced manufacturing, energy and environmental sectors. Due to our ongoing success securing large-scale projects, we now have a requirement for an Operational Support Engineer to support client site, providing day-to-day manufacturing operations support to Upstream and Downstream production. Who Are We PM Group is an employee owned, international project delivery firm with a team of 4.000+ people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients and trade partners. Responsibilities Provide manufacturing operations support to Upstream and Downstream production lines to ensure safe, compliant and reliable manufacturing. Troubleshoot and resolve manufacturing issues across mechanical/process/utility and automation interfaces, escalating as required and coordinating multi-discipline support. Drive structured problem solving (e.g., 5-Why/Fishbone) to identify root cause and implement effective corrective and preventive actions. Own and track issues through to closure using site systems (deviations, CAPAs, change controls, work orders), maintaining clear status visibility for stakeholders. Support line performance through monitoring of key operational metrics, trend analysis, and identification of recurring issues/opportunities for improvement. Ensure all activities are executed in accordance with GMP, EHS and site procedures, with a strong focus on data integrity and right-first-time documentation. Support maintenance planning and execution (including troubleshooting support during interventions), ensuring equipment is returned to service safely and compliantly. Contribute to commissioning/qualification and continuous improvement initiatives as required from an operational perspective (e.g., SOP updates, risk assessments, operational readiness). Communicate effectively with Operations, QA, Engineering, MS&T and vendors to align priorities and support business needs. Provide flexible operational support, which may include shift working, extended hours, weekend coverage and/or on-call support as business needs require. Qualifications Degree or trade background in Mechanical, Process, Chemical, Automation, or related engineering discipline (or equivalent experience). Experience supporting biopharmaceutical manufacturing operations (Upstream and/or Downstream), with strong exposure to GMP environments. Demonstrated troubleshooting capability across equipment, process and compliance issues, with an ability to prioritise in a fast-paced production setting. Strong working knowledge of deviation investigation, CAPA, change control and documentation standards (including data integrity expectations). Familiarity with CMMS/work order systems and maintenance coordination; experience with single-use and/or stainless-steel processing equipment is beneficial. Excellent stakeholder management and communication skills, with a collaborative, hands-on approach to supporting business needs. Flexibility to support shift patterns and operational coverage requirements (including potential extended hours/weekends/on-call) as the business requires. Why PM Group? As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy. Click here to read more in our Corporate Responsibility and Heath, Safety & Well-being Report. Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future. PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. xsokbrc If you require any assistance in this regard, please let us know. #LI-SG1 TLNT1_IJ

Mechanical Automation and Maintenance Fitting Apprentice (Ardnacrusha) Launch your career working on some of the largest equipment that helps power the nation Join Our Team at Ardnacrusha! This is an opportunity to work as part of a leading-edge team in Ireland's Ardnacrusha hydropower generating station and on the Shannon Scheme. Please make sure you read the following details carefully before making any applications. We have been generating electricity on the Shannon since 1929. The station team plays a pivotal role in ensuring Ardnacrusha's safety, commercial and technical performance is optimised. ESB Ardnacrusha Station has 3 Francis turbines and 1 Kaplan Type Turbine, 4 generators (G1 - G4: rated at 21MW, 22MW, 19MW and 24MW respectively) and responsibility for all the associated dams, weirs, gates, and civil structures associated with the Shannon hydroelectric scheme. ESB is committed to and promotes an open and inclusive culture where everybody has the opportunity to work to the best of their ability and feel part of the team. ESB is inviting those interested to apply for our Apprenticeship ( Mechanical Automation and Maintenance Fitting) programme which will commence in September 2026. Our apprenticeship programme will provide you with: both on-the-job and classroom-based learning dynamic work experience the skills required to undertake routine power plant maintenance as well as diagnose and problem-solve complex power plant faults attain a recognised Level 6 Trade Advanced Certificate with a world-class Utility Company What an ESB Apprenticeship consists of: The Apprenticeship is SOLAS standards-based, consisting of 208 weeks / 4-year duration. During the 4 years, there are 7 SOLAS Phases: Phases 1, 3, 5 and 7 are on-the-job training, gaining experience while working closely with qualified Crafts people on site. SOLAS Phases 2, 4 and 6 are off-the-job training modules. These phases take place in regional Education & Training Boards centres, SOLAS approved training centres and in the Technical Universities. Additional plant required training is provided by ESB in your location and at various training centres in the region. Full PPE and tools are provided along with safety training. Safety is a foundational capability of ESB and you will be expected at all times to work within and according to safe working practices and safety systems. You will be provided with safety training during your apprenticeship which is provided by ESB. You will also be required to complete safety training that is required under legislation while working in ESB. The Mechanical Automation and Maintenance Fitting Apprentice role includes, but is not limited to: learning to maintain pumps, seals, bearings, actuators, turbines, piping and pumping systems. working with hydraulics, pneumatics, workshop equipment such as lathes, drilling machines, welders, milling machines, rotating plant and equipment. You will be involved in scheduled plant maintenance programs during shutdowns. learning to trouble shoot mechanical systems during breakdowns and work as part of an experienced team of qualified technicians. An apprenticeship with ESB is an opportunity to earn while you learn to gain an internationally recognised advanced level six trade certificate. You will be supported throughout your On the Job and Off the Job phases during your training. Educational Requirements: To start your career in power generation, we are looking for candidates who have a mechanical aptitude, enjoy problem solving or technical subjects, or have an interest in working in industrial environments. Prior trade experience is not necessary, although candidates need to be safety focused, a team player, curious or technically minded and a willingness to learn are essential. Candidates must be17 years of age or older before the 1st June 2026andhaveobtained the followingminimum standards at the time of applying: Junior Cycle Profile of Achievement - 5 Achieved grades or higher in Maths, English or Irish, Science * and two other subjects. Junior Certificate - 5 grades D or higher Maths, English or Irish, Science * and two other subjects. Leaving Certificate Applied - 120 or more Credits. Vocational Leaving Certificate - 5 grades D's or higher in Maths, English or Irish, Science * and two other subjects. Leaving Certificate - 5 grade O6 or higher (formerly 3 Leaving cert grade D or higher) in Maths, English or Irish, Science * and two other subjects(H7 is not accepted as equivalent to O3 for this Campaign, a candidate must have a minimum of 40% in required subject either in higher or ordinary level) FETAC/QQI Level 3 Major Awards - Minimum 6 modules which include Communications, Mathematics or Broader Application of Number and Functional Mathematics, Personal Effectiveness or Personal and Interpersonal Skills. FETAC/QQI Level 4 Major Awards - Minimum 5 modules. FETAC/QQI Level 5 Major Awards - Minimum 5 modules. Science * can be replaced by Technology, Art, Craft & Design, Technical Graphics, Metalwork, Material Technology (Wood) Design Communication Graphics, Construction, Engineering, Home Economics, AgScience, Biology, Physics, Chemistry Additional Requirements: Full driving license or evidence of working towards a full driving licence If successful at interview stage, the successful candidate will also be required to complete a medical assessment which must be passed. Closing Date Closing date for applications is no later than 18/05/2026 If you have any queries, please e-mail: There is no commitment to a role in ESB upon completion of the apprenticeship. Note: Applicants who anticipate requiring assistance or reasonable accommodations for any part of the application or interview process may contact, in confidence, ESB is an equal opportunity employer Join us in our mission to achieve a net-zero electricity system by 2040. ESB is Ireland's leading energy utility, with activities spanning electricity generation, transmission and distribution, energy supply, energy services and international consultancy. Operating in Ireland, Northern Ireland and Great Britain, we invest over €1 billion each year to deliver a new energy future based on reliable, affordable zero-carbon electricity. Our inclusive culture fosters innovation and connection among our 9,000 employees. At ESB, we support you to be your best so that you can truly make a difference. .buttontext4ebea33125a0ecd0 a{ border: 1px solid transparent; } .buttontext4ebea33125a0ecd0 a:focus{ border: 1px dashed #009DE0 !important; outline: none !important; } Diversity, Equity and Inclusion Statement ESB is committed to being an equal opportunities employer. We welcome applications from all sections of society and ensure that no one is discriminated against on the grounds of race, religion or belief, ethnicity or nationality, disability, age, citizenship, marital status, domestic or civil partnership status, sexual orientation or gender identity, or any other basis as protected by law. Applicants who anticipate requiring assistance or reasonable accommodations for any part of the application or interview process may contact, in confidence, . About ESB Join us in our mission to achieve a net-zero electricity system by 2040. ESB is Ireland's leading energy utility, with activities spanning electricity generation, transmission and distribution, energy supply, energy services and international consultancy. Operating in Ireland, Northern Ireland and Great Britain, we invest over €1 billion each year to deliver a new energy future based on reliable, affordable zero-carbon electricity. To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process click the Continue to Application or Login/Register to apply button below. TLNT1_IJ

Quality Assurance Validation About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. Below, you will find a complete breakdown of everything required of potential candidates, as well as how to apply Good luck. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn . Are you driven to make a real difference in the lives of patients? We are seeking individuals who thrive in dynamic environments, embrace new ideas and are committed to making a meaningful impact. Location and Working Environment This position is 100% onsite in Tralee, Ireland. Purpose & Scope The role is part of the Quality Assurance function within the Astellas Ireland Co. Ltd. Tralee Plant Aseptic Manufacturing Facility. The QA Validation resource will be primarily responsible for the implementation, execution, and assessment of quality systems, procedures, and records to support compliant GMP operations. Responsibilities include ensuring adherence to agency regulations (GxP) and guidance, industry best practices, local regulations, and internal policies and procedures. This position works closely with Validation, Engineering, Manufacturing, Facilities, Document/Data Management, Quality Control (QC) and other GxP supporting functions to ensure compliance. This is accomplished by direct collaboration and oversight of Validation, Facilities/Engineering, Manufacturing Operations, QC activities and the review/audit of data and reports as specified by Standard Operating Procedures. Role and Responsibilities Build strong cross-functional relationships to ensure clear quality requirements and effective collaboration from project start. Provide hands-on QA oversight to staff and contractors, ensuring compliance with SOPs and GxP standards. Review and approve validation lifecycle documentation (plans, specifications, risk assessments, protocols, reports, deviations, and change controls). Partner with validation and stakeholders to define strategies, support project execution, and ensure timely, high-quality facility readiness in a cGMP environment. Author, review, and manage QA documentation and quality system records (SOPs, deviations, CAPA, change controls), including leading investigations and audits. Support leadership, external communications, and quality culture development while ensuring regulatory engagement and continuous improvement. Required Qualifications Science based degree with experience in a cGMP compliance environment, experience of QA function in an aseptic manufacturing plant essential. What awaits you at Astellas? Global collaboration and connection with like-minded life-science leaders. Real-world patient impact through transformative therapies. Relentless innovation at the forefront of scientific advancement. A culture of growth that supports your development and ambitions. Our Organizational Values and Behaviors Impact Innovation Integrity One Astellas Accountability Courage Sense of Urgency Outcome Focus Benefits Learn more at: We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help. #LI-Tralee #LI-Onsite #LI-LG1 To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register. TLNT1_IJ

Mechanical Automation and Maintenance Fitting Apprenticeship ( Aghada Generation Station ) Launch your career working on some of the largest equipment that helps power the nation Join Our Team at Aghada Generation Station! Are you an ambitious, high-performing individual looking to develop your trade skills in a dynamic and professional environment? ESB Aghada Power Station in Cork consists of a 450 MW Alstom single shaft combined cycle gas turbine and 3 x 90 MW Alstom dual fuel open cycle gas turbines. Do you have the right skills and experience for this role Read on to find out, and make your application. This is your opportunity to join a positive and achievement-focused workforce, where you can learn, grow, and make a significant impact. Apply now and be part of our journey towards a sustainable energy future! ESB is committed to and promotes an open and inclusive culture where everybody has the opportunity to work to the best of their ability and be feel part of the team. ESB is inviting those interested to apply for our Apprenticeship (Mechanical) programmes which will commence in September 2026. Our apprenticeship programme will provide you with: both on-the-job and classroom-based learning dynamic work experience working in a modern power plant the skills required to undertake routine power plant maintenance as well as diagnose and problem-solve complex power plant faults attain a recognised Level 6 Trade Advanced Certificate with a world-class Utility Company What an ESB Apprenticeship consists of: The Apprenticeship is a structured SOLAS standards-based, consisting of 208 weeks / 4-year duration. During the 4 years, there are 7 SOLAS Phases: Phases 1, 3, 5 and 7 are on-the-job training, gaining experience while working closely with qualified Crafts people on site. SOLAS Phases 2, 4 and 6 are off-the-job training modules. These phases take place in regional Education & Training Boards centres, SOLAS approved training centres and in the Technical Universities. Additional plant required training is provided by ESB in your location and at various training centres in the region. Full PPE and tools are provided along with safety training. Safety is a foundational capability of ESB and you will be expected at all times to work within and according to safe working practices and safety systems. You will be provided with safety training during your apprenticeship which is provided by ESB. You will also be required to complete safety training that is required under legislation while working in ESB. The Mechanical Automation and Maintenance Fitting Apprentice role includes, but is not limited to: learning to maintain pumps, seals, bearings, actuators, turbines, piping and pumping systems. working with hydraulics, pneumatics, workshop equipment such as lathes, drilling machines, welders, milling machines, rotating plant and equipment. You will be involved in scheduled plant maintenance programs during shutdowns. learning to trouble shoot mechanical systems during breakdowns and work as part of an experienced team of qualified technicians. An apprenticeship with ESB is an opportunity to earn while you learn to gain an internationally recognised advanced level six trade certificate. You will be supported throughout your On the Job and Off the Job phases during your training. Educational Requirements: To start your career in power generation, we are looking for candidates who have a mechanical aptitude, enjoy problem solving or technical subjects, or have an interest in working in industrial environments. P rior trade experience is not necessary, although you will need to be safety focused, a team player, curious or technically minded and a willingness to learn are essential. Candidates must be17 years of age or older before the 1st June 2026andhaveobtained the followingminimum standards at the time of applying: Junior Cycle Profile of Achievement - 5 Achieved grades or higher in Maths, English or Irish, Science * and two other subjects. Junior Certificate - Grade D or higher Maths, English or Irish, Science * and two other subjects. Leaving Certificate Applied - 120 or more Credits. Vocational Leaving Certificate - 5 grades D's or higher in Maths, English or Irish, Science * and two other subjects. Leaving Certificate - 5 grade O6 or higher (formerly 3 Leaving cert grade D or higher) in Maths, English or Irish, Science * and two other subjects(H7 is not accepted as equivalent to O3 for this Campaign, a candidate must have a minimum of 40% in required subject either in higher or ordinary level) FETAC/QQI Level 3 Major Awards - Minimum 6 modules which include Communications, Mathematics or Broader Application of Number and Functional Mathematics, Personal Effectiveness or Personal and Interpersonal Skills. FETAC/QQI Level 4 Major Awards - Minimum 5 modules. FETAC/QQI Level 5 Major Awards - Minimum 5 modules. Science * can be replaced by Technology, Art, Craft & Design, Technical Graphics, Metalwork, Material Technology (Wood) Design Communication Graphics, Construction, Engineering, Home Economics, AgScience, Biology, Physics, Chemistry Additional Requirements: Full driving license or evidence of working towards a full driving licence. If successful at interview stage, the successful candidate will also be required to complete a medical assessment which must be passed. Closing Date Closing date for applications is no later than 18/05/2026 There is no commitment to a role in ESB upon completion of the apprenticeship. Note: Applicants who anticipate requiring assistance or reasonable accommodations for any part of the application or interview process may contact, in confidence, ESB is an equal opportunity employer Join us in our mission to achieve a net-zero electricity system by 2040. ESB is Ireland's leading energy utility, with activities spanning electricity generation, transmission and distribution, energy supply, energy services and international consultancy. Operating in Ireland, Northern Ireland and Great Britain, we invest over €1 billion each year to deliver a new energy future based on reliable, affordable zero-carbon electricity. Our inclusive culture fosters innovation and connection among our 9,000 employees. At ESB, we support you to be your best so that you can truly make a difference. .buttontext4ebea33125a0ecd0 a{ border: 1px solid transparent; } .buttontext4ebea33125a0ecd0 a:focus{ border: 1px dashed #009DE0 !important; outline: none !important; } Diversity, Equity and Inclusion Statement ESB is committed to being an equal opportunities employer. We welcome applications from all sections of society and ensure that no one is discriminated against on the grounds of race, religion or belief, ethnicity or nationality, disability, age, citizenship, marital status, domestic or civil partnership status, sexual orientation or gender identity, or any other basis as protected by law. Applicants who anticipate requiring assistance or reasonable accommodations for any part of the application or interview process may contact, in confidence, . About ESB Join us in our mission to achieve a net-zero electricity system by 2040. ESB is Ireland's leading energy utility, with activities spanning electricity generation, transmission and distribution, energy supply, energy services and international consultancy. Operating in Ireland, Northern Ireland and Great Britain, we invest over €1 billion each year to deliver a new energy future based on reliable, affordable zero-carbon electricity. To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process click the Continue to Application or Login/Register to apply button below. TLNT1_IJ

Mechanical Project Engineer We are hiring a Mechanical Project Engineer to support the delivery of mechanical installations within healthcare and hospital environments across Ireland. Apply below after reading through all the details and supporting information regarding this job opportunity. This site-based role in Dublin involves close coordination with project, design, and site teams to ensure systems are delivered safely, efficiently, and in full compliance with regulatory and quality standards. If you are a Mechanical Project Engineer who is looking for your next career move, send your CV to Kate OHerlihy or call for a confidential discussion. Responsibilities Review mechanical drawings, specifications, and submittals for accuracy and compliance Support design development and resolve technical queries Assist procurement with equipment selection and material approvals Monitor on-site installations to ensure quality, safety, and adherence to specifications Coordinate with subcontractors, suppliers, and multidisciplinary teams Support development of method statements and risk assessments Requirements Bachelors degree in Mechanical Engineering (or equivalent) 5+ years experience in mechanical building services or construction engineering Experience working in live healthcare or hospital environments Strong knowledge of HVAC systems, piping, and mechanical installations Ability to interpret technical drawings and solve engineering issues Proficiency in MS Office and BIM tools (e.g., Revit, Navisworks) Knowledge of Irish/EU construction standards and regulations Benefits Salary: €55,000 €65,000 DOE Pension contribution Further education support Annual bonus Opportunities to work across Europe Company laptop If you are a Mechanical Project Engineer who is looking for your next career move, send your CV to Kate OHerlihy or call for a confidential discussion. All applications will be treated in the strictest of confidence. xsokbrc We also have many other roles available within the Engineering and Construction sector across Ireland and Europe. Skills: Mechanical Project Engineer Construction Engineering TPBN1_IJ

Senior Quality Assurance Associate Shift RK5335 Contract 12 months Dublin Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. Check out the role overview below If you are confident you have got the right skills and experience, apply today. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. This role plays a pivotal role in the site's Quality Assurance team. As the Quality point of contact for manufacturing and inspection operations, the PQA Senior Associate will contribute to continuous improvement initiatives by undertaking additional responsibilities beyond routine QA duties. This 24/7 shift role demands a 12-hour shift pattern (4 on, 4 off) to support manufacturing operations. Key Responsibilities: Ensure adherence to safety standards and SOPs in all activities. Review and approve production batch records and associated documentation for Qualified Person disposition activities. Provide real-time quality oversight and support for production unit operations, extending to formulation, vial and syringe Fill Finish activities, including media fills and assessment of aseptic interventions. Conduct inspections of vials and syringes as part of AQLs, annual reserve inspections, and support complaint investigations. Offer Quality Assurance support for on-the-floor investigations and deviations. Review and approve deviations for closure, ensuring compliance with appropriate documentation. Participate in customer complaint investigations. Conduct routine Quality Assurance walks on the production floor. Review and issue logbooks, ensuring compliance with procedures. Provide training and guidance to staff for effective performance. Review and approve cGMP records, ensuring compliance with appropriate documentation. Support continuous improvement and Operational Excellence initiatives. Undertake other tasks/projects as assigned by the manager. Education and Experience: University degree in an Engineering or Science-related discipline (preferred). Over 4 years of relevant experience in the pharmaceutical or biotechnology industry or an equivalent combination of experience and educational background Demonstrated problem-solving abilities, particularly in supporting non-conformance/deviation investigations. Experience in inspecting vials and syringes and engaging in aseptic operations. xsokbrc If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information. TLNT1_IJ

Senior Technician Quality Control Shift RK25920 Contract 11 months Carlow Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. Be one of the first applicants, read the complete overview of the role below, then send your application for consideration. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Key Responsibilities: Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP. Required to drive compliance with Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions Participate in QC Tier 1 daily meetings and ensure effective communication of testing progress, deviations etc Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same Operate as part of the QC team performing the allocated testing and laboratory-based duties Perform various analytical techniques including but not limited to HPLC, (HIC, CE, IEX, HP-SEC), Capillary Electrophoresis and other compendial test methods in compliance with GMP requirements Peer review testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved Participate in the laboratory aspects of OOS investigations Provide support with audit/inspection requirements to ensure department compliance/readiness. Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility. Drive continuous improvement, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues e.g., FMEA, Fishbone diagrams, 5 why's etc, Work collaboratively to drive a safe and compliant culture on site. Education and Experience: Bachelors Degree or higher preferred; ideally in Analytical Chemistry/ Biochemistry or a closely related discipline 2- 3 years experience in a pharmaceutical laboratory, ideally with experience in HPLC and relevant systems and software. Core to the role is to perform testing of samples to support the release of our key drug products. xsokbrc Good working knowledge of HPLC systems and software is desirable Good knowledge of cGMP, GLP, Quality Management Systems If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information. TLNT1_IJ

An exciting opportunity has arisen for a Process Science Lead Technician to join our client, a BioPharmaceutical Manufacturing company, based in the Mid- West. Do you have the following skills, experience and drive to succeed in this role Find out below. The Successful applicant will have the opportunity to work as part of a successful and progressive company that puts individual development at the forefront and promotes from within to achieve a high performing team . This Global company offers many training paths, including LEAN and leadership development, and actively encourage innovation and participation in continuous improvement and project work. If you are looking for a challenging and rewarding role that will help grow your skills and advance your career in Biopharma , then you might be the perfect fit for this Process Science Lead Technician About the role The main responsibility of the Process Science Lead Technician is to manage a team of 3- 4 Lab Technicians .You will coordinate the team so that productivity, quality, documentation, work schedules, safety and housekeeping is run at maximum efficiency. Responsibilities Lead a team of 3-4 Lab Technicians Conduct 1 to 1s with staff and guide development plans. Complete performance reviews and provide feedback. Ensure that the manufacturing schedules are met, producing correct volume requirements. Problem solving of manufacturing equipment to achieve product quality and production schedules. Ensuring that productivity, quality, and cost objectives are achieved. Ensuring conformance with all relevant GMP policies and procedures. Responsible for supporting cell culture and downstream purification projects including set-up of equipment and material preparation. Requirements Relevant third level qualification (Degree/Diploma)in an Engineering/ Science / Manufacturing discipline Minimum 2 years work experience in an Engineering / Manufacturing GMP environment essential Experience with pharmaceutical and/or laboratory operations (GMP, Documentation, Autoclaves, Sample Management) For further details of this exciting opportunity please apply today! Applicants are advised to APPLY NOW to avoid disappointment. xsokbrc Interviews are taking place next week. You may have searched for job titles: QC Lab Technician job Munster, QC Chemist job, QC Analyst job Limerick, QC Lab Job, Process Science Job, QC Analyst Job, Lab Analyst Job Skills: Process Science Technician Lab Tech Job Bioprocessing Technician Benefits: Benefits TLNT1_IJ