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EHS Project Engineer - Ireland, Dublin - 12 Month ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a EHS Project Engineer. What you'll do: Ensure compliance with EHS regulations including HSA and EPA.Develop and maintain assigned EHS programs and provide support for other programmes.Deliver technical EHS training to projects, engineering, operations, and laboratory staffMaintain EHS documentation including risk assessments, SOPs, and change control records.Collaborate with Engineering, Quality, and Operations to ensure alignment on EHS goals. What you'll need: Bachelor’s degree in Environmental Engineering, Chemical Engineering, Occupational Safety, Industrial Hygiene, or a related technical discipline.Extensive EHS experience in pharmaceutical, biotech, medical device or chemical manufacturing environments supporting projects/operations.Proven experience supporting capital projects, facility upgrades, and equipment installations with EHS integration.Demonstrated involvement in GMP-regulated operations and cleanroom environments.Proficient with Construction Safety and associated regulations and requirements. If this role is of interest to you, please apply now!

Design Manager - Germany, Frankfurt - 12 Month ContractThis is your opportunity to work for a global data centre operator that has been recognised for as one of fastest growing and well-known groups in the industry.Having received significant investment, this established data centre group is in their next phase of growth and require the expertise of a Design Manager. They have established partnerships with many of the well-known technology powerhouses and tailor to their development to their client's requirements.  What you'll do: Lead the full design lifecycle, ensuring design packages, standards and specifications meet strategic objectives and technical requirements.Oversee procurement and vendor selection, guiding regional project leads and driving value engineering.Manage cross‑functional design coordination, integrating all design changes and ensuring alignment across internal and external stakeholders.Drive continuous improvement, quality assurance, and risk mitigation through on‑site inspections, lessons‑learned processes, and technical oversight. What you'll need: Extensive experience in data centre design management or equivalent engineering leadership roles.Strong technical knowledge of critical cooling and power infrastructure within data centre environments.Familiarity with European construction markets, building codes, and fire ordinances.Bachelor’s degree in construction management, building services engineering, or related technical field (or equivalent experience). If this role is of interest to you, please apply now!#LI-ID1

Clean Utilities and Validation Specialist - Romania - 12 Month ContractDo you want the opportunity to work with an international pharmaceutical organisation based in Romania? If yes, then this is the assignment for you!Our client that specialises in producing generic pharmaceutical products for patients across the globe are currently seeking the expertise of a Clean Utilities and Validation Specialist.What you'll do: Lead the full Qualification lifecycle for clean utilities, including WFI, purified water, purified steam, and distribution systems.Review and refine URS, Validation Plans, and IQ OQ PQ documentation.Oversee Validation activities during FAT, SAT, installation, and commissioning.Ensure all activities meet GMP and Quality expectations while supporting a live production environment. What you'll need: Extensive experience in pharmaceutical or sterile injectable manufacturing.Strong Validation background with full CQV lifecycle experience.Direct experience with WFI, purified water, purified steam, filtration, and distribution loops.Proven ability to deliver Validation Plans, URS review, and IQ OQ PQ documentation.Experience working on projects where production could not be stopped. If this role is of interest to you, please apply now! #LI-EA1

Design Manager - UK, London - 12 Month ContractThis is your opportunity to work for a global data centre operator that has been recognised for as one of fastest growing and well-known groups in the industry. Having received significant investment, this established data centre group is in their next phase of growth and require the expertise of a Design Manager. They have established partnerships with many of the well-known technology powerhouses and tailor to their development to their client's requirements.  What you'll do: Lead the full design lifecycle, ensuring design packages, standards and specifications meet strategic objectives and technical requirements.Oversee procurement and vendor selection, guiding regional project leads and driving value engineering.Manage cross‑functional design coordination, integrating all design changes and ensuring alignment across internal and external stakeholders.Drive continuous improvement, quality assurance, and risk mitigation through on‑site inspections, lessons‑learned processes, and technical oversight. What you'll need: Extensive experience in data centre design management or equivalent engineering leadership roles.Strong technical knowledge of critical cooling and power infrastructure within data centre environments.Familiarity with European construction markets, building codes, and fire ordinances.Bachelor’s degree in construction management, building services engineering, or related technical field (or equivalent experience). If this role is of interest to you, please apply now! #LI-ID1

Senior Process Quality Excellence Specialist - UK, West London - 12 Month ContractWe are looking for an experienced Senior Process Quality Excellence Specialist for a fantastic 12 month contract based in West London. You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease. This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first. What you’ll do: Manage Regulatory Intelligence (RIN) requirements for GCSO and coordinate with relevant SMEs.Review regulations and assign SMEs based on topic expertise.Serve as point of contact to ensure CROs assess all applicable regulatory and country‑specific requirements.Act as Audit Host, coordinating internal audits and supporting SMEs during auditor interactions.Support post‑audit activities, including responses to findings, CAPAs, and audit closure. What you’ll  need: Ideal candidates have experience as a Clinical Trial Associate or Clinical Trial Specialist.Exposure to audits is highly desirable.Regulatory Intelligence experience is a strong advantage.A blend of clinical operations background and quality/regulatory awareness is preferred.Overall, candidates should bring a mix of clinical trial support, audit familiarity, and regulatory insight. If this role is of interest to you, please apply now! #LI-KT1

Senior Automation Engineer - US, Raleigh - Long Term ContractDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Senior Automation Engineer for their Raleigh, NC based location.   What you'll do: Lead specific area (example Upstream, Utilities, Downstream…) as automation ownerParticipate in site business planning as an Automation representative.Lead vendor FATs as automation representsEnsure that site and global standards are met. What you'll need: Extensive experience in a manufacturing environment, biopharmaceutical or pharmaceutical industry, or an equivalent combination of education and experience.Knowledge of S95 Level 1 systems such as Emerson Delta V, OSI Pi, PLCs, IT Infrastructure & Hardware.DeltaV Batch Control experience.Knowledge of Industrial Automation Networks and their Communication Protocols. If this role is of interest to you, please apply now!#LI-MC1

Data Manager - Ireland, Dublin - 11 Months Initial ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Data Manager. What you'll do: As a Data Manager, you will be vital in building our animal data models, working closely with Marketing, IT, and R&D leads and teams to explore the data our products upload to our data platform.You will innovate new data features and work with data scientists to create innovative farm and animal KPIs promoting animal health and well-being.You will be responsible for data quality and integrity, ensuring our data is up-to-date and of high value.Conduct data profiling, analysis, and validation to ensure the accuracy, completeness, and consistency of animal health data. What you'll need: Extensive hands-on experience working as a Data Steward, Data Manager, Data Custodian, or similar role.Experience with data management tools and technologies, such as Collibra, Immuta, and Data BricksExperience harvesting data from ERP and CRM systems such as SAP and Salesforce, with a proven track record of building complex customer data models in international corporations.Strong knowledge of veterinary medicine and animal health data management principles If this role is of interest to you, please apply now!#LI-CH3

Project Engineer (LAPI) - 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 Project Engineer to join the team and help deliver this world-class program. What you’ll do: Support workshops and document outcomesCoordinate stakeholders for HSE initiatives (e.g., LOTO)Support solvent introduction planning and executionAssist with PSSR and startup readiness  What you’ll need: Bachelor’s degree in Engineering or a related technical fieldExtensive project experience in GMP, construction, or engineering environmentsExperience supporting execution (not just planning)Strong communication, initiative, and stakeholder coordinationFamiliarity with PSSR, LOTO, solvent handling, or C&Q is a plus Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Operational Readiness PM - 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 Operational Readiness Project Manager to join the team and help deliver this world-class program. What you’ll do: Own and lead operational readiness planning and execution for assigned areas of the Medicine Foundry.Partner with Manufacturing, Quality, Engineering, Validation, Supply Chain, EHS, IT, and other site functions to define readiness scope and deliverables.Translate operational readiness requirements into structured, executable plans and schedules.Build, manage, and maintain operational readiness schedules aligned with construction, commissioning, and qualification milestones. What you’ll need: Bachelor’s degree in Engineering, Chemistry, or related scientific/technical discipline.Extensive experience in pharmaceutical or biotech manufacturing environments.Direct experience supporting operational readiness, startup, or commissioning of a new or expanded manufacturing facility.Strong understanding of manufacturing operations and how key site functions interact (Operations, Quality, Engineering, Validation, Supply Chain). Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1