Explore global engineering opportunities

Drug Product Engineer (Formulation) - 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 Drug Product Engineer. What you'll do: Provide technical and compliance review and/or authorship of testing protocols, reports, and applicable manufacturing SOPs.Generate and execute documentation for cGMP activities including risk assessments /reports. Management of Equipment Vendors including execution of on-site maintenance visits, management of continuous improvement projects & spare parts criticality assessments.Support/lead maintenance of the validated state of the equipment through execution of revalidation protocols as per Site VMP. What you'll need: Extensive cGMP industrial / engineering experience, Experience in executing on the floor activities such as FAT, SAT, IQ/OQ Specific experience with Autoclave, Parts Washers, and CIP/SIP equipment. Knowledge of Formulation processes. If this role is of interest to you, please apply now!#LI-CH3

Utilities Engineer - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Utilities 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: Support the Critical Utilities Operations and Maintenance team in the day-to-day operation and maintenance of utility equipment.Assist in developing and updating plant operation procedures, maintenance plans, and risk assessments.Help ensure maintenance standards are met to support safe and reliable operations.Review vendor documents and reports, and assist with closing out Work Orders in the site CMMS. What you’ll need: Bachelor’s Degree (Level 8) in a relevant Science or Engineering discipline.Extensive experience providing technical support on an operating site; experience in biopharmaceutical manufacturing is an advantage.Basic knowledge of utility system design, installation, maintenance, and troubleshooting, with the ability to interpret technical documents and process drawings.Basic Knowledge of Good Manufacturing Practices, maintenance systems, and industry regulations related to pharmaceutical manufacturing is desirable. If this role is of interest, please apply now!#LI-JS4

Senior CQV Engineer - Ireland, Dublin - 12 Month ContractOur client is a global leader in pharmaceutical innovation, specializing in the development and manufacture of cutting-edge drugs. As they continue to grow, they’re seeking an experienced Senior CQV Engineer to join their dynamic team and drive forward groundbreaking projects in Dublin. What you’ll do: Ensure Commissioning readiness of Utility Systems to support Equipment Start-up and IOQ Testing, acting as CQV SME on Utility systems.Lead CQV interface with KNEAT.Liaise with all Project Groups to ensure all Systems are managed appropriately for the Project Lifecycle.Support CQV Document Generation. What you’ll need: Extensive experience including experience with design and construction projects for pharmaceutical manufacturing facilities.Experience within Black Utilities.Experience utilising electronic validation systems including KNEAT. Apply today and be part of shaping the future of medicine!#LI-TE1

Validation Engineer - 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 Validation Engineer . What you'll do: Support the site validation activities across a number of workstreams.Develop and maintain the site Validation Master Plan.Drive development of site EMPQ strategy and implement/maintain EM protocols and procedures for graded pharmaceutical areas, ensuring compliance with regulatory guidelines.Support equipment qualification post Operational Qualification (OQ) through to Process Performance Qualification (PPQ) and subsequent revalidation.  What you'll need: Extensive direct experience with a pharmaceutical or biotechnology company with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.Bachelor’s degree (or higher) in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry etc.Prior experience in Cleaning Validation, Temperature Mapping activities, and qualification of Parts Washers and/or Autoclaves.Experience with upstream cell culture and/or downstream formulation/fill finish processes. If this role is of interest to you, please apply now!#LI-CH3

CQ Engineer PMO - Germany - 18 Month Contract Looking to take your career to the next level? We’re recruiting for a high-impact pharmaceutical project located near Germany. With major capital investment experience driving various facility build projects. This is a unique opportunity for a CQ Engineer PMO to join a global leader in the life sciences market and play a key role in shaping the future of advanced manufacturing. What you’ll do: Support C&Q activities while acting as the team’s PMO specialistOwn and maintain these systems end-to-end, ensuring accuracy, usability, and scalabilityCollaborate with cross-functional teams to ensure project transparency and timely deliveryProvide technical guidance and training to team members on PMO tools What you’ll need: Proven expertise in Microsoft Excel, MS Project, Tableau, and SmartsheetStrong understanding of project lifecycle within pharmaceutical or GMP-regulated environmentsExperience in commissioning and qualification of pharmaceutical equipment or facilitiesAbility to work independently and proactively in a fast-paced project environment Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-CO1

CQ Engineer - Germany, Frankfurt - 8-9 Months Initial ContractLooking to take your career to the next level? We’re recruiting for a high-impact pharmaceutical project located near Frankfurt. With major capital investment experience driving various facility build projects. This is a unique opportunity for a CQ Engineer to join a global leader in the life sciences market and play a key role in shaping the future of advanced manufacturing. What you’ll do: Execute FAT protocols for Syntegon liquid/aseptic filling lines and autoclave sterilizers.Review and approve vendor FAT protocols, test scripts, and acceptance criteria.Execute mechanical, automation, and functional testing—including safety, alarms, interlocks, and recipe functionality.Document deviations, non-conformances, and corrective actions; ensure timely resolution prior to equipment shipment. What you’ll need: Previous FAT execution experience, strong preference for Filling equipment however the Manager is open to reviewing strong EngineersExtensive hands on CQ experienceP&ID redline and punch list experienceKnowledge and experience with KNEAT Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-CO1

Senior Piping & Process Engineer - Belgium, Antwerp - 10 Months Initial ContractDo you want to work with a world leader in material technology? This opportunity is currently available to a Senior Piping & Process Engineer to support our clients growing portfolio of projects globally across material science, chemistry and metallurgy. With a portfolio of exciting projects coming up globally, there is no better time to join this exciting company – make your application today for immediate consideration. What you'll do: Designing the installation from concept, through basic engineering until detailed engineering and execution. Processing all input from stakeholders. Sometimes, you will also manage external engineering firms.Conducting technical discussions with suppliers (preparing technical specifications, price inquiries, orders, and tracking deliveries).Estimating costs and creating a schedule in consultation with the project manager, and monitoring these during execution.Coordinating execution works and general site activities. Keeping and resolving a punch list until the project is fully completed. What you'll need: A bachelor's degree with a specialisation in electromechanics or mechanical engineering.Strong knowledge of pumps, piping (both calculations and design), and thermodynamics.Strong knowledge of process engineeringSeveral years of relevant work experience. If this role is of interest to you, please apply now! #LI-CT2

Manufacturing Projects Scientist Engineer - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Manufacturing Projects Scientist 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: Contribute to cross functional teams (Manufacturing, Engineering, QA, QC, Regulatory, Supply Chain, etc.) for process improvement implementations, new product start-ups or other process changes.Support new product introduction risk assessments to ensure the appropriate controls are in place to enable manufacturingSupport product change over protocols to allow a smooth transition from sustaining to new product manufacturingRepresent the Manufacturing at meeting to ensure the end user requirements are represented What you’ll need: Ability to demonstrate proficiency communicating and collaborating at a variety of levels, coupled with excellent organization and planning skills.Currently completing a Bachelors/Masters in Science, Engineering, or a related subject.In-depth theoretical knowledge of GMP biologics manufacturing equipment and process automation.Proven ability to support the closeout of complex technical investigations.Strong working knowledge of systems such as Delta V, MES Syncade and SAP. If this role is of interest, please apply now!#LI-JD1

Process Engineer - Belgium, Brussels - 7 Month Initial ContractWe are looking for an experienced Process Engineer for a fantastic 7 month contract based in Brussels. 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: Planning of all the technical activitiesFollow-up of the implementation of the corrective actions. re-test when needed.Support SAT activities in its area of expertiseReview and approve the updated technical documentationOrganise the training of the final user in its area of expertise & provide technical documentation in to finalise the Hand-over What you’ll  need: Extensive experience within pharmaceutical companies and working with Engineering officesIn-depth technical experience in a regulated environment, biologicals, pharmaceutical and engineering operationsExperience in single use systems within the pharmaceutical industryLarge experience in equipment installation and commissioningGood understanding of EHS (Environment, Health and Safety) and Quality aspects (GMPs) If this role is of interest to you, please apply now!#LI-CB1