Ready to power the future of biopharmaceutical manufacturing? We’re looking for an experienced Senior Electrical & Instrumentation Project Engineer to lead essential electrical projects, ensuring our site remains safe, compliant, and innovative. What you’ll do: Design and manage LV/ELV systems (lighting, fire alarms, data points, UPS, automation) Drive small-scale electrical infrastructure projects from concept to completion Collaborate in design reviews, testing, and installations Prepare and update electrical drawings and documentation Specify and deliver cGMP-compliant E&I equipment and controls Integrate electrical systems with business IT networks Lead contractor supervision, risk assessments, and Health & Safety initiatives Your expertise: Degree in Electrical Engineering (or similar) Experience in regulated manufacturing (ideally biopharma) Strong project management and technical skills Passion for safety, teamwork, and continuous improvement #J-18808-Ljbffr
EFOR is seeking a Senior Electrical & Instrumentation Project Engineer in Limerick, Ireland, to lead critical electrical projects. The successful candidate will design and manage low voltage systems, ensure compliance with safety standards, and oversee project execution in a regulated biopharmaceutical environment. Candidates should have a degree in Electrical Engineering and experience in regulated manufacturing. This role offers opportunities for significant professional growth and contribution to innovative projects. #J-18808-Ljbffr
Project Engineer – Aseptic Manufacturing (Biopharma/API) Looking to advance your engineering career in cutting-edge biopharma? We’re seeking a Project Engineer with proven aseptic manufacturing experience to join our dynamic team focused on delivering complex API and biopharmaceutical projects. Your Role Manage and support multi-disciplinary projects in aseptic and sterile manufacturing environments Oversee project phases from design, installation, and commissioning to qualification and validation Coordinate vendors, contractors, and internal teams to realize project objectives on time and within budget Ensure all project activities align with GMP, quality, and safety requirements Identify and implement process improvements, troubleshooting issues to drive operational excellence Prepare and review technical documentation for regulatory compliance What You Bring Degree in Engineering or related discipline Hands-on experience delivering projects in aseptic, sterile, or cleanroom manufacturing (biopharma or API a plus) Solid understanding of GMP guidelines and regulatory standards for pharmaceutical manufacturing Strong organizational, communication, and stakeholder management skills Problem-solving mindset and keen attention to detail Ready to make a real impact in the world of biopharma and APIs? Apply today to join a company where innovation and quality are at the heart of what we do! #J-18808-Ljbffr
EFOR in County Cork is looking for a Project Engineer specializing in aseptic manufacturing within the biopharma industry. The ideal candidate will manage complex projects, ensuring compliance with GMP guidelines and driving operational excellence. Responsibilities include coordinating internal teams and overseeing project phases from design to validation. A degree in Engineering and hands-on experience in sterile environments are essential for this role, which offers a chance to impact biopharma innovation significantly. #J-18808-Ljbffr
The CSA Engineer is responsible for providing civil, structural and architectural engineering leadership on the Project, ensuring that all CSA design, construction and completion activities are delivered safely, on time, to specification and within budget. The role provides technical oversight and assurance of the CSA scope from Basis of Design (BOD) through construction and handover, working closely with the Client Engineering team, EPCM partners, contractors and specialist subcontractors to ensure integrated, compliant delivery across all buildings and site‑wide infrastructure. CSA Design Oversight & Technical Assurance Provide client‑side CSA engineering oversight across all buildings and site‑wide civil infrastructure, from Basis of Design (BOD) through detailed design. Review and challenge EPCM and specialist consultant deliverables for structural design, architectural specifications, civil and drainage design, ensuring compliance with Eurocodes, Dutch building regulations, Global Engineering Standards and project‑specific requirements. Ensure CSA design inputs are coordinated with process, mechanical, HVAC, E&I and fire protection disciplines; identify and resolve clashes and interface issues through design reviews and BIM coordination. Support value engineering and buildability reviews to optimise CSA solutions for cost, schedule and constructability without compromising quality or compliance. Oversee geotechnical and ground condition assessments, ensuring foundation design and earthworks solutions are appropriate for the site conditions (including any UXO, contamination or groundwater considerations). Construction Support & Site Oversight Provide CSA engineering support during construction, including review of contractor method statements, temporary works proposals, lifting plans and structural steelwork erection sequences. Monitor CSA construction quality on behalf of the client, ensuring workmanship, materials and finishes meet specification and that non‑conformances are identified, documented and resolved. Support resolution of site‑based technical queries (TQs) and requests for information (RFIs) relating to CSA scope; assess proposed changes for structural and architectural impact. Coordinate with Construction Management and Leads to ensure CSA works are sequenced correctly relative to MEP installations, process equipment placement and clean‑build requirements. Review and approve as‑built documentation, structural completion certificates and handover packages for CSA scope. Ensure all CSA design and construction activities comply with Dutch building regulations, Eurocodes (EN 1990–1999), fire safety codes and environmental permit conditions. Support the environmental permitting process (Omgevingswet / BOPA application) by providing CSA‑related inputs including building envelope specifications, drainage design, landscape and visual impact assessments as required. Maintain awareness of local planning conditions and ensure architectural design respects any site‑specific constraints (height restrictions, façade treatments, landscaping buffers, noise attenuation). Ensure GMP‑relevant architectural elements (room classifications, finishes, cleanability, containment) are incorporated into the design and maintained through construction. Integrated Planning & Stakeholder Coordination Contribute to integrated schedule development by providing realistic CSA activity durations, sequencing logic and long‑lead procurement inputs (e.g., structural steel, cladding, specialist finishes). Coordinate with procurement and EPCM teams on CSA package strategy, technical bid evaluation and vendor/subcontractor selection. Communicate CSA progress, risks and issues clearly to Leads, the Project Director and wider stakeholder groups through regular reporting and design/construction review meetings. Build effective working relationships across the contractor teams to facilitate rapid resolution of CSA‑related issues. Safety, Environmental & Risk Leadership Promote a strong safety culture and ensure CSA design and construction activities align with EHS policies, including safe design principles, CDM‑equivalent obligations and working‑at‑height risk management. Identify, assess and manage risks across the CSA scope including ground conditions, structural interfaces, weather dependencies, material supply and subcontractor performance. Support hazard identification and elimination through design (e.g., fall protection, structural stability during construction phases, temporary works design review). Ensure environmental mitigation measures (dust, noise, vibration, water management) are incorporated into CSA construction methodologies. Required Qualifications & Experience Bachelor’s degree (or higher) in Civil Engineering, Structural Engineering, Architecture or a related discipline. Chartered Engineer status (CEng) or equivalent professional registration is strongly preferred. Proven experience (typically 10+ years) in CSA engineering on large‑scale industrial, pharmaceutical or advanced manufacturing facility projects. Demonstrable experience across structural design review, construction oversight and handover on multi‑building greenfield programmes. Strong working knowledge of Eurocodes (EN 1990–1999), and familiarity with Dutch or European building regulations. Experience working within EPCM delivery models alongside international engineering contractors. Excellent communication, coordination and stakeholder management skills; ability to work effectively in a multi‑disciplinary, multi‑cultural project environment #J-18808-Ljbffr
EFOR is looking for an MES Engineer in Sligo, Ireland, to drive digital transformation within pharmaceutical manufacturing. The role involves implementing and supporting MES solutions, integrating them into existing systems, and ensuring compliance with industry regulations. Ideal candidates should have a Bachelor's degree in Engineering or a related field, experience with MES platforms, and excellent communication skills. Join a pioneering team that offers growth opportunities and the chance to make a significant impact in delivering lifesaving medicines. #J-18808-Ljbffr
EFOR in Munster, Ireland is seeking a DeltaV Commissioning Engineer for biopharma facilities. The role involves leading commissioning processes, executing operational protocols, and troubleshooting automation systems. Candidates should have 3–5 years of site-based commissioning experience, strong hands-on DeltaV expertise, and excellent communication skills. This is an exciting opportunity to contribute to the future of biopharmaceutical manufacturing. #J-18808-Ljbffr
DeltaV Commissioning Engineer – Biopharma Facility Ready to make an impact in biopharma manufacturing? We're looking for DeltaV Engineers to drive hands‑on commissioning of process and utility areas across four API trains at our advanced facility. Your Role: Lead DeltaV commissioning—from equipment module setup and recipe validation through OQ Execute operational protocols in full integration with the C&Q team Troubleshoot and optimize automation systems to ensure seamless process delivery What You Bring: 3–5 years site‑based commissioning experience (biopharma/API preferred, but not essential) Strong hands‑on DeltaV expertise Proven record in equipment module and recipe commissioning Excellent teamwork and communication skills Important: Site‑based commissioning experience is mandatory. Candidates must meet this requirement to be considered. Bring your expertise—help us shape the future of biopharmaceutical manufacturing! Apply now. #J-18808-Ljbffr
Job Title: MES Engineer – Pharmaceutical Manufacturing Location: Sligo, Ireland Overview Join our dynamic team as an MES Engineer, where you’ll drive digital transformation in pharmaceutical manufacturing. You will play a key role in designing, deploying, and optimizing Manufacturing Execution Systems (MES) to ensure production excellence and compliance with industry standards. Key Responsibilities Implement and support MES solutions to streamline production workflows Integrate MES with equipment, ERP, and quality systems Collaborate with cross-functional teams to define and improve processes Troubleshoot MES issues and deliver technical solutions Ensure regulatory compliance (GMP, FDA, etc.) in MES operations Requirements Bachelor’s degree in Engineering, Computer Science, or related field Experience with MES platforms (e.g., Werum, Siemens, Rockwell, etc.) Pharma manufacturing or GMP environment background desirable Strong communication, analytical, and problem-solving skills Why Join Us? Be part of a pioneering pharma team that leverages technology to deliver lifesaving medicines more efficiently. Shape your future with opportunities for growth, innovation, and impact. #J-18808-Ljbffr
A global pharmaceutical leader in Cork is seeking a Primary Packaging Scientist to enhance innovations in pharmaceutical packaging. The role includes providing expertise in packaging materials, designing and validating packaging for drug products, and ensuring compliance with quality and safety standards. Ideal candidates should have a Master’s or PhD in Science or Engineering and experience with primary packaging for pharmaceuticals. Join a team committed to excellence in packaging solutions. #J-18808-Ljbffr
