Senior Process Engineer | API Manufacturing Expansion Project Cork, Ireland Site-Based ENG Bauen is supporting a leading global pharmaceutical company in delivering a major expansion project, requiring an experienced Process Engineer to oversee critical process evaluations within an API manufacturing environment. This is an opportunity to play a key role in a high-value investment program, ensuring that Commissioning, Qualification, and Validation (CQV) activities align with production requirements. Our client is making significant investments in state-of-the-art manufacturing technology to enhance production efficiency and maintain world-class pharmaceutical standards. As part of this strategic expansion, they require a Process Engineer to act as a key interface between CQV teams, Quality Assurance, and production operations, ensuring all process changes comply with regulatory and operational standards. This is an excellent long-term opportunity within a company at the forefront of pharmaceutical manufacturing advancements. Key Responsibilities: Act as the voice of production in evaluating CQV activities, ensuring new systems and modifications meet operational needs. Pre-approve qualification documents, verifying compliance before final QA sign-off. Assess and verify instrumentation changes, including valves, temperature sensors, and process control systems. Update P&IDs to reflect modifications within the production area. Ensure that all process changes align with GMP, safety, and regulatory standards. Required Skills & Experience: Degree in Chemical Engineering, Process Engineering, or related discipline. Strong experience in API manufacturing and process engineering within the pharmaceutical sector. Working knowledge of CQV principles, with experience in assessing qualification work from a production perspective. Familiarity with GMP, regulatory compliance, and quality assurance processes. Hands-on experience with valves, temperature sensors, and instrumentation systems. Ability to interpret and update P&IDs in response to system modifications. If you are interested in this opportunity, please apply or send your CV via the ENG Bauen website or LinkedIn page. Keywords: Process Engineer, API Manufacturing, Pharmaceutical Process Engineer, CQV Process Engineer, GMP Process Engineer, API Compliance Engineer, Process Control Engineer, Commissioning & Qualification Engineer, P&ID Engineer, Process Validation Engineer, Chemical Process Engineer, API Site Engineer. #J-18808-Ljbffr
Digital Transformation Lead | Pharmaceutical Project Tipperary, Ireland ENG Bauen is partnering with a leading global pharmaceutical company on an exciting capital project to support their digital transformation. We are seeking a Digital Enablement Lead to spearhead the integration of cutting-edge digital solutions within the manufacturing environment, ensuring that the facility is equipped for future advancements. This is a high-impact role that will see you lead the delivery of digital initiatives across a major expansion project. You will be working closely with cross-functional teams to define the scope and requirements for a truly state-of-the-art, digitally-enabled facility. This role offers a fantastic opportunity to take a leading position in a transformative project and contribute to shaping the future of pharmaceutical manufacturing. The role: Lead the scoping and delivery of digital initiatives, ensuring alignment with the project’s overarching goals and timelines. Work closely with local site stakeholders and global product teams to identify the required digital capabilities for the facility. Collaborate with technical teams to ensure that all digital solutions are implemented effectively, with a focus on optimizing operational efficiency. Oversee the integration of advanced digital technologies and systems, ensuring they meet regulatory and operational standards. Provide technical leadership and guidance, ensuring the successful adoption and implementation of digital tools across the site. The person: Strong experience in digital enablement within the pharmaceutical, biotech, or similar regulated industries. Proven track record of successfully managing digital initiatives and integrating technology solutions within large-scale projects. Excellent communication and stakeholder management skills, with the ability to drive cross-functional collaboration. Knowledge of digital tools and platforms used in manufacturing environments, with an understanding of shop-floor systems like DeltaV, OSI-PI, and MES. Ability to work effectively with both technical and non-technical teams to deliver high-quality results. If you are interested in finding out more about the role, please apply or send your CV via the ENG Bauen website or LinkedIn page. #J-18808-Ljbffr
2 days ago Be among the first 25 applicants Direct message the job poster from ENG Bauen Business Manager | UK & EMEA Region | Global Project Execution Expertise Ireland | Long-term Contract ENG Bauen has been working closely with our clients, supporting capital projects across the Life Sciences, Pharmaceutical, and Energy sectors. As part of our continued growth, we are seeking skilled professionals to join high-impact projects that are shaping the future of pharmaceutical manufacturing. We are partnering with a leading pharmaceutical organisation that is making significant investments in cutting-edge pharmaceutical and biotech manufacturing. As part of its growth strategy, the company is undertaking complex capital expenditure projects at one of its key sites in Ireland. With project values ranging from €50M to €250M, these initiatives are focused on enhancing manufacturing capabilities, expanding production facilities, and advancing life sciences technologies. The successful candidate will be instrumental in ensuring that all systems, equipment, and processes comply with regulatory requirements while supporting the seamless transition from construction to fully validated production environments. The role: Lead CQV activities for automation and IT aspects of capital projects. Develop and execute validation plans, protocols (IQ, OQ, PQ), and reports. Ensure compliance with industry regulations (GMP, FDA, EMA) and company quality standards. Collaborate with cross-functional teams, including Engineering, Quality, and Operations, to drive validation strategies. Conduct risk assessments, gap analyses, and remediation planning. Provide technical expertise in commissioning and qualification (C&Q) activities, ensuring efficient project delivery. The Person: Bachelor's degree in Engineering, Computer Science, or a related technical field. Extensive experience in CQV roles within the Pharmaceutical, Biotech, or Life Sciences sector. Strong knowledge of validation principles, including laboratory analytical instrument qualification. Hands-on experience with automation and IT systems used in pharmaceutical manufacturing. Excellent communication and stakeholder management skills, with the ability to present technical findings effectively. If you are an experienced CQV Engineer looking for an opportunity to be at the forefront of pharmaceutical innovation, apply now to be part of these transformative projects. Seniority level Mid-Senior level Employment type Contract Job function Manufacturing, Engineering, and Consulting Industries Pharmaceutical Manufacturing, Engineering Services, and Automation Machinery Manufacturing #J-18808-Ljbffr
Senior Delta V Automation Engineer | Pharmaceutical Project County Tipperary, Ireland Site based As ENG Bauen expands its support for clients across the UK and Europe, we are offering an exceptional opportunity for an experienced Delta V Engineer to take on a long-term position with a client who is making significant investments in transformative improvement and upgrade projects within the pharmaceutical sector. Our client is a globally recognised leader in the pharmaceutical and biopharmaceutical industries, renowned for its innovative approaches to drug development, manufacturing, and supply chain management. As part of their ongoing growth and investment in state-of-the-art facilities, they are enhancing their project delivery capabilities, ensuring the highest standards of operational excellence. As the Senior Delta V Engineer, you will serve as the key technical authority, responsible for driving the successful delivery of the automation and IT scope across the entire CAPEX project lifecycle. You will lead the technical execution of all automation activities, ensuring that systems are implemented to the highest standards while meeting the company’s strategic goals. This role is tailored for Senior Automation professionals with a proven track record in managing end-to-end automation projects in the pharmaceutical, biotech, or biopharma sectors. You will bring your expertise to lead the Delta V programming, integration, and recipe-building processes from the ground up, ensuring that automation systems deliver operational excellence. Key Responsibilities: Lead and manage the automation scope for the project, ensuring that all Delta V DCS systems are delivered on time, within budget, and in compliance with industry regulations. Act as the main point of contact for automation-related deliverables, collaborating closely with internal teams and external stakeholders. Oversee the design, implementation, and commissioning of Delta V systems, ensuring optimal performance across critical operations. Provide technical leadership and mentoring to the automation team, driving efficiency and maintaining a high standard of work. Ensure the automation systems comply with all safety, quality, and compliance standards, while meeting project timelines and business objectives. Be an active contributor to the successful delivery of the full project scope, from design through to final handover. Required Skills & Experience: Bachelor's degree or equivalent in Automation Process Control, Computer Science, Software Engineering, or a related field. A minimum of 7+ years of experience in automation engineering, with a focus on Delta V systems within the pharmaceutical, biotech, or biopharma industries. Expertise in Delta V programming, recipe building from scratch, and system integration. Strong leadership and project management skills, with a track record of delivering complex automation projects in regulated environments. In-depth understanding of GxP and industry regulations, with a focus on compliance and quality assurance. Excellent communication and interpersonal skills to manage stakeholder relationships and lead teams effectively. If you are interested in finding out more about the role, please apply or send your CV via the ENG Bauen website or LinkedIn page. #J-18808-Ljbffr
Direct message the job poster from ENG Bauen Business Manager | UK & EMEA Region | Global Project Execution Expertise Ireland | Long-term Contract On-site Position for a Delta V Automation Engineer to join a new high-value project from the early stages of design, where you will be responsible for the overall delivery of multiple Automation Systems at a global leading Biopharmaceutical organisation. This is the ideal role for an automation professional who has a strong background in delivering automation systems from design to commissioning and can coordinate with all internal and external vendors to ensure project delivery. You will work closely with systems integrators and engineering vendors to ensure all deliverables meet project needs and to liaise with senior stakeholders on the project to ensure clear lines of communication. This is a fantastic opportunity for an Automation Engineer to step into a long-term contract position with a client investing heavily in the improvement and upgrade projects. The position: 12 month contract position – 2 year project assignment Client site position Supporting DCS systems interfacing with PLC systems Ensuring all software is compliant with S88 standards The ideal applicant for the role: 5 plus years of DCS configuration and testing required Ability to work within a high-performing team Must have a background in Automation (full life cycle) Strong experience in DeltaV, PLCs, HMIs and OSI PI Experience with recipe testing If you are interested in finding out more about the role, please apply or send your CV via the ENG Bauen website or LinkedIn page. Seniority level Mid-Senior level Employment type Contract Job function Engineering, Design, and Production Industries Pharmaceutical Manufacturing, Engineering Services, and IT Services and IT Consulting #J-18808-Ljbffr
