A leading recruiter in the pharmaceutical sector is seeking a CSV Engineer in Dublin. The ideal candidate will have over 5 years of experience in CSV within regulated environments and possess strong knowledge of FDA regulations. This on-site role offers an hourly rate of €75–80, requiring expertise in computer system validation and risk assessments. Join a dynamic team to ensure compliance and data integrity in a fast-paced industry. #J-18808-Ljbffr
This range is provided by Atrium (EMEA). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base Pay Range Direct message the job poster from Atrium (EMEA) Duration: 12 Months Working hours: 39 hours per week Onsite requirements: Onsite Engagement Type: LTD Company Contractor Hourly rate: 75–80 EUR per hour Legal Right to Work: You must have the legal right to work in Ireland. No sponsorship is available for this role. Atrium Global is supporting a client within the pharmaceutical industry to appoint a highly skilled CSV Engineer. This position plays a key role in ensuring regulated systems, laboratory software, analytical instruments and manufacturing technologies meet full compliance across the business. Job Overview You will take ownership of end-to-end computer system validation activities, working across Quality, IT, Laboratory and Manufacturing teams. This role involves developing validation protocols, managing qualification of analytical instruments, supporting audits and ensuring that all systems meet the highest standards of data integrity and regulatory compliance. It is an excellent opportunity for an experienced CSV specialist with strong exposure to QC laboratories, PAT, enterprise laboratory systems and paperless validation tools. Responsibilities Develop and execute IQ, OQ and PQ protocols for computer systems, laboratory instruments and software applications. Partner with IT, QA and Operations to maintain compliance with regulatory guidelines and internal quality systems. Conduct system-level risk assessments and impact analyses. Create and manage validation documentation including plans, test scripts, traceability matrices and summary reports. Perform periodic reviews to ensure sustained compliance. Support change control by assessing validation impact and defining required activities. Provide subject matter expertise on CSV principles, regulations and best practice. Monitor updates to regulatory expectations and industry trends. Work with vendors to ensure external systems meet validation standards. Support audits and inspections by preparing and presenting CSV evidence. Lead qualification of analytical instruments including Cell Viability Analysers, Liquid Handlers and other QC laboratory technologies. Requirements Bachelor’s degree in Computer Science, Engineering or a related field. Strong working knowledge of FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. 5+ years of CSV experience in a regulated pharmaceutical or biotechnology environment. Understanding of risk-based validation methodologies. Proven experience creating and executing validation protocols with high-quality documentation. Strong analytical and problem‑solving skills with excellent attention to detail. Confident communication skills with the ability to work across multiple functions. Ability to manage several projects simultaneously and independently. Understanding of SDLC, change control and data integrity principles. Experience supporting sterile drug product manufacturing environments and associated laboratory and IT systems. Must‑Haves Extensive experience delivering CSV from requirements through release of analytical instruments used in QC laboratories or PAT‑based manufacturing operations. Strong background validating server or database‑based laboratory software, middleware and enterprise applications such as LIMS, Empower and NuGenesis. Demonstrated experience completing Electronic Record Electronic Signatures (ERES) assessments and Data Integrity Risk Assessments. Hands‑on experience using paperless validation and test management tools including ValGenesis, Kneat and ALM. Seniority Level Mid‑Senior level Employment Type Contract Industries Pharmaceutical Manufacturing, Biotechnology Research, and Manufacturing Get notified about new Computer Systems Engineer jobs in Dublin, County Dublin, Ireland. #J-18808-Ljbffr
A leading biotechnology company in Dublin is seeking a Senior Electrical Engineer for their pharmaceutical manufacturing site. The role involves overseeing electrical systems, ensuring compliance, and leading technical teams. Candidates should have at least 10 years of experience in the pharmaceutical sector, along with strong leadership and engineering skills. A hybrid working model is offered, alongside a competitive salary package. #J-18808-Ljbffr
Senior Electrical Engineer – Pharmaceutical Manufacturing Base pay range Direct message the job poster from Atrium (EMEA) Onsite requirements: Hybrid – approx. 50% onsite over a two-week period Engagement Type: Permanent (contract or contract-to-perm option also available) Benefits: €30,000 bonus package, full benefits + LTI (permanent option) Salary: Up to €100,000 per annum DoE Hourly Rate: €75 per hour (contracting option) - This is a contract to permanent option Legal Right to Work: All applicants must have the legal right to work in Ireland. No sponsorship is available. Atrium Global is partnering with a leading organisation in the biopharmaceutical sector to hire a Senior Manager – Site Electrical SME for a large biologics manufacturing campus in Dublin 15. This is a senior technical leadership role where you will oversee all electrical systems, special systems, life safety and security systems across GMP and non-GMP facilities. This position offers the chance to lead electrical design governance, drive engineering excellence and play a major role in delivering complex capital projects across a world‑class manufacturing site. Job Overview You will act as the site’s primary Electrical Subject Matter Expert, responsible for design review, engineering compliance, construction support and commissioning oversight. Working with engineering, construction, project management and CQV teams, you will ensure the safe, compliant and reliable delivery of electrical systems across the entire site. Responsibilities Serve as the key electrical discipline lead and main point of contact for the project team Provide SME oversight for electrical, special systems, life safety and security systems Review and approve electrical drawings, datasheets, specifications and technical documentation Ensure all electrical work complies with regulatory, quality, EHS and engineering standards Act as system owner for electrical systems across GMP and non-GMP areas Participate in design reviews, 3D model reviews, HAZOPs, FATs, SATs and construction walkdowns Review vendor packages and technical submissions for electrical and special systems Guide A&E partners and contractors to ensure design compliance and execution quality Lead electrical SWAT activities, commissioning readiness and punch list closure Oversee TTOPs, VTOPs and support CQV documentation to full closure Support drawing management and handover processes Lead development and review of electrical bid packages and construction scopes Maintain Basis of Design intent throughout project execution Manage electrical‑related budgets, schedules and engineering milestones Approve commissioning protocols and support electrical troubleshooting during startup Provide technical guidance for maintenance strategies and lifecycle planning Liaise with cross‑functional groups to ensure full alignment across engineering, construction and operations Support schedule development, acceleration strategies and risk mitigation Ensure correct inspection, storage, installation protection and construction quality for electrical systems Participate in inspections, first‑in‑place reviews, mechanical completion and punch list evaluation Requirements Degree in Electrical Engineering or equivalent Qualified Electrician with strong industrial experience Minimum 10 years’ experience in pharmaceutical manufacturing (design, construction, commissioning, operations) Extensive experience in MV/LV distribution, generators, UPS, lighting/emergency lighting, containment, voice/data, fire alarm, earthing/bonding, lightning protection, hazardous areas and life safety/security systems Strong understanding of electrical engineering codes, standards and best practice Experience delivering complex projects within operational GMP facilities Proven SME capability in troubleshooting and supporting electrical systems in a regulated environment Strong leadership, communication and cross‑functional coordination skills Proficiency in MS Project, AutoCAD, Navisworks, SAP, Visio, BMS platforms and standard engineering tools Experience coordinating electrical planning and scheduling across multiple buildings and facilities Seniority level Mid-Senior level Employment type Full-time Job function Biotechnology Research, Pharmaceutical Manufacturing, and Manufacturing #J-18808-Ljbffr
This range is provided by Atrium (EMEA). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Direct message the job poster from Atrium (EMEA) Onsite Requirements: Fully onsite, 5 days per week Engagement Type: PAYE contract Hourly Rate: €38.51 per hour Atrium Global is partnering with our client, a leading global biopharmaceutical organisation dedicated to developing innovative medicines and advancing patient care. We are seeking an experienced QA SME to support their Quality function in Cruiserath for a 9-month PAYE assignment. Job Overview The QA SME will support the Qualified Person with batch certification activities and ensure all quality standards are met in compliance with SOPs, regulatory requirements, and internal quality systems. This role plays a key part in maintaining inspection readiness and supporting continuous improvement initiatives across the site. RESPONSIBILITIES Support the Qualified Person with the Batch Certification function. Prepare and review batch documentation packages for QP release as per SOP requirements. Liaise with Supply Chain and Quality teams to ensure timely disposition of batches. Update SOPs and controlled documents (FORMS, OJTs) as required. Assist with new product introduction activities. Provide training to new team members. Support site inspection readiness for corporate and regulatory audits. Identify and recommend opportunities for continuous improvement. Participate in Quality Management System activities (Change Control, Self-Inspections, Quality Agreements, Customer Complaints, Product Quality Reviews). Ensure all activities comply with SOPs, GMP regulations, and Quality Agreements. Perform additional team tasks to support the effective running of the function. REQUIREMENTS Degree in Science, Engineering, or a related discipline (essential). Minimum 1–2 years’ experience in the pharmaceutical or biopharmaceutical industry. Experience with data or document management systems (e.g. DCA, Trackwise, Infinity, SAP). Strong working knowledge of Microsoft Excel and PowerPoint. Excellent organisational skills and attention to detail. Ability to work independently as well as collaboratively within a team. Capable of managing multiple priorities and meeting deadlines. Demonstrates initiative, adaptability, and commitment to continuous improvement. Legal Right to Work Applicants must have the legal right to work in Ireland. Visa sponsorship is not available for this role. Seniority level Mid-Senior level Employment type Contract Job function Quality Assurance Biotechnology Research Pharmaceutical Manufacturing Manufacturing #J-18808-Ljbffr
Senior Specialist, QA Compliance – Materials Management Duration: 8 months (until 31 July 2026 – fixed term, backfill for leave cover) Working Hours: 39 hours per week Onsite Requirements: Initially 5 days onsite; hybrid working (up to 50% from home) once trained Engagement Type: Via PAYE Hourly Rate: €28.41 per hour Atrium Global is partnering with one of our leading biopharmaceutical clients to recruit an experienced Senior Specialist, QA Compliance – Materials Management. This position supports material qualification and release activities for a state‑of‑the‑art biologics manufacturing facility, contributing to both its commercial portfolio and clinical pipeline. Job Overview Reporting to the Senior Manager, QA Compliance, the successful candidate will be responsible for quality assurance activities related to materials management, ensuring compliance with cGMP standards and internal quality systems. The role requires strong collaboration across teams, excellent organisational skills, and the ability to meet accelerated timelines in a fast‑paced biologics environment. Responsibilities Prepare, review, and approve Material Qualification Documentation. Perform QA disposition of raw materials and consumables (Level 1 & Level 2). Author, review, and approve QA‑related procedures. Conduct QA review, assessment, and approval for Biologics Manufacture documentation, including: Change controls Deviations and investigations CAPAs TSE (Transmissible Spongiform Encephalopathy) Certificates Other relevant quality records Act as a core member of the QA Compliance Materials Management team. Support Operational Excellence initiatives (e.g., 5S, Standard Work, Kaizen, Problem Solving). Requirements BSc in Science or a related discipline. Minimum of 3 years’ QA or related experience in a Biologics or Pharmaceutical environment. Strong understanding of cGMP requirements for manufacturing and compliance systems. Knowledge of material qualification and SAP is highly desirable. Proven ability to work independently and collaboratively across teams. Excellent communication, presentation, and organisational skills. Strong time management and multitasking abilities. Demonstrated commitment to continuous improvement and operational excellence. Legal Right to Work: Candidates must have the legal right to work in Ireland. No visa sponsorship is available for this position. Seniority level Mid‑Senior level Employment type Contract Job function Quality Assurance Industries Biotechnology Research Pharmaceutical Manufacturing Manufacturing #J-18808-Ljbffr
Private Equity Fund Team Leader – Limerick Overview Atrium is looking for a Private Equity Specialist to assist in all aspects of the administration of Private Equity Funds including fund accounting, transfer agency and financial reporting. The role involves ensuring that allocated clients receive a high‑end, timely and effective service. The Private Equity Team Leader will take over an existing client list, become proficient in delivering end‑to‑end fund administration, complete reviews to maintain the department’s high standards, and mentor other analysts in the team. Responsibilities Assist in managing an expanding Private Equity team Execute strategic plans, goals and priorities Deliver high‑quality service to each assigned client Qualifications Previous experience in an accounting environment Good track record of producing financial statements and reviews Team player, customer‑centric with excellent attention to detail, positive attitude, enthusiasm, and the ability to work under pressure and meet tight deadlines Excellent communication skills Hold a recognised Professional Accounting Qualification or equivalent post‑QE experience Detailed knowledge of Irish/UK GAAP, US GAAP and IFRS Working knowledge of the Irish regulatory and tax regime as it relates to fund accounting and financial reporting Knowledge of or willingness to quickly gain knowledge of Private Equity Fund Administration Demonstrated leadership and team‑building qualities, with the ability to motivate a team Clear and concise communication skills Strong knowledge of Microsoft Office – Excel and Word Track record of excellent attention to detail Experience in optimising system use and automating processes where possible Provision of focused, quality client service Commitment to producing high‑quality work within required timeframes Willingness to support daily BAU activities when necessary Ability to participate in systems development projects Ability to assist in developing a team in a Tier 3 location Next Steps Click Apply now to be considered for the Private Equity Fund Team Leader – Limerick role. #J-18808-Ljbffr
