E, A & I Integration lead

Process & Piping Integration Lead - US, Ohio - 12 Month ContractBe part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility in Ohio, a multi-billion-dollar investment designed to push the boundaries of science and engineering. We’re looking for a Process & Piping Integration Lead to join the team and help deliver this world-class program. What you’ll do: Lead owner-side integration of process, piping, and equipment engineering scopes.Coordinate closely with the Owner Equipment Manager on equipment data, layouts, and installation requirements.Transition from design integration to discipline-focused construction support.Ensure piping and equipment systems are designed for cleanability, testability, and access. What you’ll need: Extensive experience in pharma, biotech, or complex regulated projects.Strong background in process systems, piping engineering, and equipment integration.Experience working with EPC delivery models and owner-side teams.Solid understanding of system-based turnover and CQV execution. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Process Utilities Integration Lead - US, Ohio - 12 Month ContractBe part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility in Ohio, a multi-billion-dollar investment designed to push the boundaries of science and engineering. We’re looking for a Process Utilities Integration Lead to join the team and help deliver this world-class program. What you’ll do: Integrate clean and dirty utility systems including WFI, PW, clean steam, process gases, HVAC utilities, chilled water, steam, condensate, waste, and drains.Challenge EPC utility designs for operability, maintainability, and sequencing.Support installation sequencing, testing, flushing, passivation, and startup activities.Ensure utility systems meet CQV access, testing, and documentation requirements. What you’ll need: Extensive experience in clean utilities and facility infrastructure for regulated projects.Strong understanding of utility system commissioning and CQV expectations.Experience working with EPCs and owner teams.Utility systems are turned over aligned with process and CQV schedules. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Tech Transfer Engineer (Downstream) - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Tech Transfer Engineer for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.What you’ll do: Deliver tech transfer readiness activities from facility assessment through to PPQ execution and report completion for a new product introduction to the MPCC Cruiserath.Authoring of technical documents, including protocols, reports and SOPs supporting the validation of the manufacturing process.Identify and implement process improvements, e.g. yield, cycle time reduction through evaluation of process performance using data analytics tools.Generate documentation protocols and lead the execution of plant supporting studies and technical studies on the manufacturing floor at commercial scaleProvide on the floor support for troubleshooting processing issues and to lead manufacturing investigations into process deviations and resolution What you’ll need: Minimum BSc or equivalent extensive experience in drug substance manufacturing technical support in the biopharmaceutical industry including tech transfer preparation, execution and post-execution activities.You have demonstrated awareness of cGMP compliance and regulatory agency requirements as well as strong oral communication and technical writing skills.Good interpersonal skills coupled with demonstrated ability to effectively work in a cross-functional global environment matrix organisation, and in local group settings.Ability to develop, build, present and defend technical and scientific approaches in both written and verbal form. If this role is of interest, please apply now!#LI-JS4

Senior Project Controls Lead - US, Maryland - 12 Months Initial Contract Our client is currently seeking the skills of a Senior Project Controls Lead to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll do: Lead and oversee project controls implementation across a major project or a portfolio of smaller projects, ensuring all organizational standards, governance expectations, and compliance requirements are met throughout the full project lifecycle.Provide proactive and transparent communication to project leadership—across both Project Services and Project Execution—highlighting performance trends, emerging risks, variances, and opportunities for corrective or preventative action.Define and maintain project controls frameworks, including service level agreements, RACI/responsibility matrices, and coordination protocols to ensure clear ownership and alignment between internal teams and external partners.Develop, maintain, and approve comprehensive project control plans and procedures covering all key discipline areas: scheduling, cost management, cashflow forecasting, risk management, change control, and project reporting. What you'll need: Extensive capital project experience, with strong technical and execution exposure on major capital investments—ideally within the pharmaceutical or biotech sector.Proven experience supporting pharmaceutical R&D capital projects, including understanding of the unique requirements, regulatory considerations, and delivery models within research environments.Demonstrated success working within a global organization, with the ability to adapt engineering and project delivery approaches to accommodate regional, cultural, and regulatory differences.Strong track record collaborating with design contractors and equipment suppliers on large-scale, complex projects, ensuring alignment, quality, and timely delivery across multidisciplinary teams. If this role is of interest to you, please apply now!#LI-SC1

Procurement Specialist - Denmark, Copenhagen - 12 Month ContractOur client, a global organisation within the pharmaceutical industry, needs a Procurement Specialist to join their large-scale CAPEX project based near Copenhagen. This is a fantastic opportunity for a professional in the life sciences sector to advancing their career within a globally recognised pharmaceutical environment. What you’ll do: Proven track record of Tendering of equipment & service agreements incl. the Evaluation and recommendations of award.Proven track record of excellent stakeholder management alignment with legal, SME’s, finance and managementActively participates in team and project environments. Encourages co-operation.Aware of needs of others and responds flexibly What you’ll need: Recognised degree and qualification within Procurement and/ or Supply Chain ManagementExperience of working within CAPEX procurement within a highly regulated project environmentStrong critical-thinking and problem-solving skills; ability to recognise, resolve discrepancies and implement resolutions to benefit the organisationMust possess the abilities to meet accelerated timelines, manage multiple shifting priorities and maximise efficiencies in a dynamic customer-focused environment Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-DC1

MS&T Scientist, Downstream - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for an MS&T Scientist for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.What you’ll do: Upstream (Cell culture focus) including media preparation, large scale cell culture bulk drug substance manufacturing process (vial thaw, scale up, single use systems, seed and production bioreactors and harvest centrifugation/clarification).Downstream: to include buffer preparation, purification and viral reduction steps including chromatography, ultrafiltration viral reduction filtration and viral inactivation technologies and DS formulation and bulk fill.Authoring of technical documents, including protocols, reports and SOPs supporting the validation of the manufacturing process.To identify and implement process improvements, e.g. yield, cycle time reduction through evaluation of process performance using data analytics tools. What you’ll need: Minimum BSc or equivalent with at extensive experience in drug substance manufacturing technical support in the biopharmaceutical industry.You have demonstrated awareness of cGMP compliance and regulatory agency requirements as well as strong oral communication and technical writing skills.Good interpersonal skills coupled with demonstrated ability to effectively work in a cross-functional global environment matrix organisation, and in local group settings.Ability to develop, build, present and defend technical and scientific approaches in both written and verbal form. If this role is of interest, please apply now!#LI-CB1

CSV Engineer - Ireland, Dublin - 12 Month Contract One of the top 10 best companies to work in Ireland is looking for a CSV Engineer for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.What you’ll do: Develop and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for laboratory analytical instruments (e.g Cell Viability Analysers etc.)Create and execute test protocols designed to verify compliance of the system with data integrity principles and regulatory requirements.Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure compliance with regulatory guidelines and internal policies.Perform risk assessments and impact analyses to identify critical system functionalities and potential vulnerabilities. What you’ll need: Bachelor's degree in Engineering, Science, Computer Science or a related field.Extensive experience in a similar roleExperience working in a similarly large biologics company, preferably within a Validation, Analytical or Quality Assurance role.Knowledge of Validation principles and processes If this role is of interest, please apply now!#LI-CB1

C&Q LOTO Officer - Denmark, Copenhagen - 12 Month ContractOur global engineering client specialise in delivering innovative solutions for the pharmaceutical and life sciences industries. Their focus is on designing and optimising advanced facilities that enable the development and production of critical medicines. With a strong commitment to quality, sustainability, and cutting-edge technology, they help clients bring life-changing treatments to patients worldwide. They are currently looking for a C&Q LOTO Officer to join their team based near Copenhagen.What you'll do: C&Q LOTO Officer is responsible for overall safety in the project management starting from Mechanical Completion, and working closely with Commissioning and Initial Startup team.Conduct risk assessment (RAMS) identifying potential hazards and mitigations as per Company and EU Standards for each process system to be ready for startup.Review project documents e.g. P&ID, Layout, ATEX mapping, safeguarding system (SGS) etc. for establishing adequate controls in place and Lock out Tag out (LOTO) on safety critical equipment for the safe execution of C&Q activities.Understand the functional safety requirements for evaluating process operating sequence and potential deviations for corrective actions is necessary. What you'll need: Extensive experience in managing Lockout/Tagout procedures to ensure the safe isolation and control of energy sources.Experience in preparing and reviewing work permits, ensuring all necessary safety measures are in place before work begins.Strong background in preparing LOTO P&I Diagrams and understanding of P&ID systems.Extensive Commissioning experience on large scale projects. If this role is of interest, apply now!#LI-EB1

CSV Engineer - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a CSV Engineer for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.What you’ll do: Develop and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for computer systems and software applications.Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure compliance with regulatory guidelines and internal policies.Perform risk assessments and impact analyses to identify critical system functionalities and potential vulnerabilities.Create and maintain validation documentation, such as validation plans, test scripts, traceability matrices, and validation summary reports. What you’ll need: Bachelor's degree in Computer Science, Engineering, or a related field.Strong knowledge of regulatory guidelines, such as FDA 21 CFR Part 11, EU Annex 11, and GAMP 5.Extensive experience in computer system validation within a regulated industry, preferably pharmaceuticals or biotechnology.Familiarity with validation methodologies, including risk-based validation approaches. If this role is of interest, please apply now!#LI-JS4