Senior Electrical Engineer – Pharmaceutical Manufacturing Onsite requirements: Hybrid – approx. 50% onsite over a two‑week period. Engagement type: Permanent (contract or contract‑to‑permanent option available). Full‑time. All applicants must have the legal right to work in Ireland. No sponsorship is available. Role: Senior Manager – Site Electrical SME for a large biologics manufacturing campus in Dublin 15. This is a senior technical leadership role overseeing all electrical systems, special systems, life safety and security systems across GMP and non‑GMP facilities. It offers a 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 (SME), 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 key electrical discipline lead and main point of contact for the project team. Provide SME oversight for electrical, special systems, life safety(cv) and security systems. Reviewopfu. drawggings, datasheets, specifications and technical documentation. Ensure all electrical work complies with regulatory, quality, EHS and engineering standards. angall Act 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&Elaser partners and contractors to ensure design compliance and execution quality.Lead electrical SWAT activities, commissioning readiness and punch list closure. Oversee TTOPs and VTOPs and support CQV documentation to full closure. Support drawing management and hand天天中奖 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 Industry: Biotechnology Research, Pharmaceutical Manufacturing, Manufacturing. Referrals increase your chances of interviewing at Atrium (EMEA) by 2×. Get notified about new Electrical Engineer jobs in Dublin, County Dublin, Ireland. #J-18808-Ljbffr
A leading pharmaceutical company in Dublin is seeking a Senior Electrical Engineer to act as the primary SME for electrical systems across their biologics manufacturing site. This mid-senior level position requires a degree in Electrical Engineering and at least 10 years of experience in pharmaceutical manufacturing. Responsibilities include ensuring compliance, managing budgets and schedules, and providing technical guidance. This full-time role offers hybrid work options and requires expertise in various electrical engineering tools and standards. #J-18808-Ljbffr
A project management firm is seeking a Senior Project Manager to oversee healthcare systems implementation in a hybrid role based in Dublin. The ideal candidate will have a Bachelor's degree in a relevant field, project management qualifications, and experience in public sector healthcare environments. Responsibilities include leading projects, managing stakeholders, and ensuring delivery on time and budget. This contract role lasts for 12 months with a focus on implementing radiology systems and ensuring governance throughout projects. #J-18808-Ljbffr
Senior Project Manager – Healthcare Systems Implementation Contract Role – Dublin/Hybrid – 12 months Role Overview Job Title: Senior Project Manager – Healthcare Systems Implementation Location: Dublin/Hybrid Contract Type: Contract Duration: 12 months (Candidates must have the legal right to work in Ireland and be currently based in Ireland) Primary Responsibilities Lead and implement customer projects from initiation through to closure Scope, plan, and deliver projects to agreed timelines, quality, and budget Scope, lead, and implement technical infrastructure projects Manage project/program stakeholders internally and customer-facing Oversee the end-to-end project lifecycle, including sales, requirements definition, contracting, initiation, and closure Create and manage project initiation documents and plans, defining scope, deliverables, budgets, timelines, milestones, and other required documentation Ensure change management processes are followed to maintain delivery within budget and maximize revenue opportunities Forecast projects and associated revenue profiles over time Implement robust governance at all levels Provide accurate and effective management information on delivery status Proactively manage risks and issues through timely identification, mitigation, and closure Support the sales team with tender responses and other sales activities as required Qualifications Required Qualifications Bachelor’s degree (or higher) in a computer science or information technology discipline Project management qualification such as Prince2 or equivalent Experience implementing radiology systems from vendor to public sector organisations (HSE/NHS) Experience delivering from vendor to public sector health systems (HSE/NHS) Proficiency with MS Project, MS Office (PowerPoint, Excel, Word, Visio) Experience delivering into a public sector healthcare environment Preferred Qualifications Experience using Smartsheets in a project delivery environment Experience with SharePoint, Jira, Confluence Ability to work with product management and software development teams Soft Skills Communication and interpersonal skills Presentation, training, and facilitation skills Flexible approach, with the ability to work on your own initiative Ability to work under pressure and meet tight deadlines Ability to coordinate multiple geographically widespread projects Please feel free to contact Daisy Nguyen at dnguyen@gibbsconsulting.com for a confidential chat to learn more details about the role. #J-18808-Ljbffr
A biopharmaceutical company is seeking a mid-senior level Commissioning Qualification Validation Engineer in Dublin. This hybrid role (50/50) requires execution of cleaning validation activities for a new product intro in a multi-product GMP facility. Candidates must have a degree in a relevant field, 2+ years in GMP environments, and direct cleaning validation experience, particularly in biopharmaceutical settings. This position offers a contract engagement with key responsibilities including sample analysis and compliance adherence. #J-18808-Ljbffr
A leading recruitment agency is seeking a CSV Engineer to support a client in the pharmaceutical and biotechnology sector. This onsite role in Dublin offers a contract for 12 months at an hourly rate of €75. The ideal candidate will have over 5 years of experience in CSV within regulated environments, demonstrating strong knowledge of FDA regulations and validation methodologies. Responsibilities include developing validation protocols, conducting risk assessments, and ensuring compliance during regulatory inspections. #J-18808-Ljbffr
Commissioning Qualification Validation Engineer Duration: 12 months Working hours: 39 hours Onsite requirements: 50/50 hybrid – onsite full time during execution phase (expected to be summer 2026) Engagement Type: LTD Company Contractor Legal Right to Work: Candidates must have the legal right to work in Ireland. This role does not offer sponsorship. This role is for a client of ours. The client operates in the biopharmaceutical drug substance manufacturing industry. Job Overview The Cleaning Validation Engineer will support cleaning validation activities for a new product introduction (NPI) tech transfer into a multi-product GMP drug substance manufacturing facility. The role will primarily focus on cleaning sampling execution, QC result correlation, and generation/approval of cleaning validation documentation within a small, specialist CQV team. Responsibilities Execute cleaning validation sampling, including swab and rinse collection. Perform sample preparation and coordinate submission to QC for analysis. Administer LIMS workflows and support sample traceability. Correlate QC results with cleaning changeover protocols and logbooks. Support product changeover and equipment release activities. Generate and standardise Energy Control Plans (ECPs) and cleaning validation documents. Assist with LOTO (Lockout/Tagout) where required. Provide investigation and troubleshooting support within QMS. Prepare and issue cleaning validation release memos. Liaise with cross‑functional teams to ensure timely approval of deliverables. Maintain compliance with site and global GMP procedures and regulatory guidelines. Deliver workstream tasks to project deadlines within a team of 4 FTEs. Requirements Minimum of a Bachelor’s degree in a scientific, technical, or engineering discipline. 2+ years of experience in a GMP environment. Hands‑on cleaning validation execution experience, with strong preference for biopharmaceutical or multi‑product facilities. Direct experience performing swab and rinse sampling. Experience in sample preparation and submission to QC. LIMS exposure or administration experience. Strong understanding of cGMP and contamination control. Ability to work onsite full time during the Summer 2026 execution period. Nice to Have Biopharmaceutical process validation knowledge. Experience in drug product filling or sterile manufacturing environments. Seniority level: Mid-Senior level Employment type: Contract Job function and industry: Engineering and Manufacturing; Pharmaceutical Manufacturing, Biotechnology Research, and Chemical Manufacturing Location: Dublin, County Dublin, Ireland #J-18808-Ljbffr
Overview Atrium Global is supporting the search for a CSV Engineer for a client in the pharmaceutical and biotechnology industry. This role is 12 months in duration with 39 hours per week , onsite on a Fully onsite basis, and engagement via LTD Company Contractors . The hourly rate is up to €75 per hour. Candidates must have the legal right to work in Ireland ; the role does not offer sponsorship. Location: Dublin, County Dublin, Ireland (onsite working arrangement). Job title: CSV Engineer . Note: This posting includes application messaging prompts and time-stamped postings; only the substantive job details above are included here. Responsibilities Develop and execute validation protocols (IQ, OQ, PQ) for computerised systems and software. Partner with IT, Quality, Operations and cross-functional teams to ensure regulatory and internal compliance. Conduct risk assessments and impact analyses to determine critical system functions and vulnerabilities. Produce and maintain validation artefacts including plans, test scripts, traceability matrices, summary and validation reports. Perform periodic system reviews to maintain ongoing regulatory compliance. Support change control activities by assessing system modifications and executing required re-validation tasks. Provide subject matter guidance on CSV principles, regulatory expectations and best practice approaches. Work with vendors to ensure validation compliance for third-party lab and production systems. Validate laboratory analytical instruments and software including QC and PAT-enabled systems. Execute ERES and Data Integrity Risk Assessments for analytical instruments and related software. Perform validation using paperless test platforms such as ValGenesis, Kneat, or ALM. Support regulatory inspections and audits with documentation readiness and CSV-focused discussions. Qualifications Bachelor's degree in Computer Science, Engineering, or related discipline. Strong working knowledge of FDA 21 CFR Part 11, EU Annex 11 and GAMP 5 (GAMP 5 required). 5+ years CSV experience in regulated Pharma or Biotech environments. Experience with risk-based validation methodologies. Proven capability in protocol execution and validation documentation practices. Understanding of SDLC, change control and data integrity principles. Experience in sterile drug product manufacturing and associated lab/production/IT systems. Mandatory CV Requirements CSV of analytical instruments in QC labs or PAT-enabled manufacturing from requirements through to release. CSV of server/database-based laboratory software, middleware and enterprise systems (e.g., LIMS, Empower, NuGenesis). Execution of Electronic Record Electronic Signature (ERES) and Data Integrity Risk Assessments. Hands-on experience using paperless validation/test tools such as ValGenesis, Kneat, or ALM (ValGenesis or Kneat required). Seniority level Mid-Senior level Employment type Contract Job function Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Chemical Manufacturing #J-18808-Ljbffr
A global biopharmaceutical company in Dublin is seeking a Senior Electrical Engineer to oversee electrical, life safety, and security systems across a biomanufacturing site. This role requires a degree in Electrical Engineering, 10+ years in pharmaceutical manufacturing, strong leadership skills, and proficiency in MS Project and AutoCAD. The position offers a hybrid work arrangement and a competitive salary package, including a bonus. #J-18808-Ljbffr
Senior Electrical Engineer – Pharmaceutical Manufacturing 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 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 Job Details Seniority level: Mid-Senior level Employment type: Full-time Job function: Biotechnology Research, Pharmaceutical Manufacturing, and Manufacturing #J-18808-Ljbffr
