Construction Piping & BIM Engineer

Planner - US, Ohio - 12 Months Initial ContractBe part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility near Ohio, a multi-billion-dollar investment designed to push the boundaries of science and engineering. We’re looking for a Planner to join the team and help deliver this world-class program. What you’ll do: Develop and manage high-level program schedules for capital projects, ensuring accurate forecasting and project alignment.Own and oversee the Owner Verification Schedule and Operational Readiness Schedule, integrating project phases and milestones.Lead schedule reviews, ensuring contractor submissions align with overall project strategy, scope, and deadlines.Conduct critical path analysis, identify risks, and provide recovery strategies to maintain project integrity. What you’ll need: Extensive experience in project scheduling and planning within large-scale CAPEX projects (pharmaceutical sector preferred).Bachelor's degree in Engineering, Project Management, Construction Management, or equivalent.Expert proficiency in Primavera P6 and MS Project.Strong understanding of EPCM contracts, project logic, and scheduling methodologies. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Contracts Administrator, Site/General Conditions - 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 Contracts Administrator to join the team and help deliver this world-class program. What you’ll do: Own the contract administration and commercial execution of assigned mechanical construction packages (e.g., HVAC, process piping, utilities/mechanical systems, mechanical install scopes).Lead/support RFP development and issuance (often in coordination with Fluor), including bidder communications, clarifications, and commercial bid evaluation.Support contract drafting/review, ensuring scope, deliverables, milestones, and commercial terms are clear and executable in the field.Manage contract award package: pricing basis, assumptions, inclusions/exclusions, schedule milestones, reporting requirements, payment terms. What you’ll need: Extensive experience in construction contracts administration / commercial management for mechanical scopes.Strong experience managing mechanical construction packages (not just processing contracts).Experience working owner-side or seconded to owner on large capital projects; EPCM interface experience strongly preferred (Fluor/Jacobs/Bechtel etc.).Comfortable operating in active construction: understands work packaging, sequencing, and mechanical interface risk. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Engineering 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 an Engineering Integration Lead to join the team and help deliver this world-class program. What you’ll do: Own and enforce horizontal integration across process, piping, utilities, E&I, and automation disciplines on behalf of the Owner.Act as the single point of accountability for engineering alignment, readiness, and system-level coherence.Validate engineering maturity based on system completeness, constructability, and CQV readiness, not percent-complete metrics.Challenge EPC engineering progress reporting that is resource-driven rather than deliverable- or system-driven. What you’ll need: Extensive experience in pharmaceutical or regulated industrial engineering environments.Demonstrated owner-side or owner’s engineer experience on large-scale CAPEX projects.Strong multi-discipline engineering integration experience within EPC or EPCM environments.Deep understanding of system-based delivery models and their impact on construction sequencing, commissioning, and CQV. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Owners Equipment Manager - 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 an Owners Equipment Manager to join the team and help deliver this world-class program. What you’ll do: Define and manage the owner equipment execution strategy aligned to project schedule, system boundaries, and CQV turnover needs.Identify critical and long-lead equipment impacting engineering development, piping release, utilities, controls, and qualification.Establish and track equipment readiness milestones aligned to P&ID development, IFC releases, mechanical completion, and system turnover.Ensure timely issuance, completeness, and stability of equipment data (datasheets, nozzles, loads, utilities, control inputs).Act as the primary owner technical interface with equipment vendors. What you’ll need: Extensive experience supporting pharmaceutical, biotech, or regulated manufacturing CAPEX projects.Demonstrated owner-side or owner’s engineer experience managing equipment lifecycle risk.Strong understanding of process and utility equipment, and their interfaces with piping, utilities, controls, and CQV.Experience managing equipment data maturity, vendor technical alignment, and FATs. Familiarity with EPC delivery models and system-based delivery concepts. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Contracts Administrator, Mechanical Packages - 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 Contracts Administrator to join the team and help deliver this world-class program. What you’ll do: Own the contract administration and commercial execution of assigned mechanical construction packages (e.g., HVAC, process piping, utilities/mechanical systems, mechanical install scopes).Lead/support RFP development and issuance (often in coordination with Fluor), including bidder communications, clarifications, and commercial bid evaluation.Support contract drafting/review, ensuring scope, deliverables, milestones, and commercial terms are clear and executable in the field.Manage contract award package: pricing basis, assumptions, inclusions/exclusions, schedule milestones, reporting requirements, payment terms. What you’ll need: Extensive experience  in construction contracts administration / commercial management for mechanical scopes.Strong experience managing mechanical construction packages.Experience working owner-side or seconded to owner on large capital projects; EPCM interface experience strongly preferred (Fluor/Jacobs/Bechtel etc.).Comfortable operating in active construction: understands work packaging, sequencing, and mechanical interface risk. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Clean Utilities Engineer - Paris, France - 4 Months Initial ContractOur client, a global pharmaceutical company, are looking for a Clean Utilities Engineer to join their team. The company has grown to become a world leader in the development, manufacture, and marketing of innovative pharmaceutical products to alleviate some of the world’s biggest health problems. What you'll do: Conduct quality activities for the Clean Utilities work packageClean utilities specialist for the MOA in the execution of turnkey contracts with our partnersAdministrative tasks for the maintenance of the Clean Utilities equipmentPreparation of the master plan for the maintenance What you'll need: Experience in Clean utilitiesExperience working in a project set upExperience working for pharmaceutical building and utilities including commissioning requirements (FAT/ SAT / QI / QO)Language is English in the project, so English full professional proficiency is mandatory If you would like to apply or find out more, get in touch now!#LI-LH1

MS&T Scientist (Upstream or 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: Have a thorough knowledge of the science behind each molecule and associated drug substance manufacturing processes with fundamental knowledge of one or more of the following relevant principles.To identify and implement process improvements, e.g. yield, cycle time reduction through evaluation of process performance using data analytics tools.Provides process subject matter expertise for regulatory inspections and other interactions with regulatory agencies (e.g. health authority query support - timely responses / data gathering etc.), representing the Cruiserath site.To provide 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 with 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-JS4

QA Analyst - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a QA Analyst 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: Execute and assist in batch release testing, technical transfer and co-validation activities.Accurately documenting laboratory work.Data review based on demonstrated proficiency on assays.Performing routine data analysis, assist in the investigation of OOS results, perform trending analysis and writing investigation reports. What you’ll need: Experience in the following analytical techniques would be an advantage: Aseptic Techniques, Cell Culture, Cell-based Bioassays and ELISA.The ideal candidate should hold a minimum of a BSc. in Biochemistry or related discipline.The successful candidate must demonstrate an ability to work independently in assay execution and recognise anomalous trends or results.The successful candidate must demonstrate problem solving ability, as well as the ability to prioritise objectives from multiple projects and adhere to scheduled timelines. If this role is of interest, please apply now!#LI-JS4

Software Application Engineer - Denmark - 6-10 Month ContractOur client, a global organisation within the pharmaceutical industry, needs a Software Application Engineerto join their large-scale CAPEX project based in Denmark. 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: URS development inputBid package and vendor reviewVendor clarification meetings and follow upVendor documentation review/approval What you’ll need: Technical background in automation and control systems with experience working in regulated GMP environmentsHands-on experience reviewing and developing Functional Specifications (FS), test documentation, and validation deliverables (IQ/OQ)Strong knowledge of PLC/SCADA platforms, HMI configuration, industrial IT/OT architecturesexperience in vendor management, including technical clarifications, documentation review, FAT/SAT participation, and ensuring alignment between requirements and delivered solutions. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-DC1