QA Analyst

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

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

CQV Engineer - Ireland, Dublin - 12 Month ContractOur client, a global pharmaceutical company, are looking for a CQV 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: Own and manage GEP documentation including Engineering Design Specifications, C&V Plans, GEP Test Sheets, and Engineering Reports.Act as project manager when required, maintaining tight control of vendor activities and deliverables.Evaluate technical design and performance of systems such as HVAC and Clean Utilities.Proactively challenge existing practices, introducing new ideas to enhance performance. What you'll need: Extensive experience in the pharmaceutical industry, with strong exposure to commissioning and qualification of GxP/GEP systems.Experience in project management and contractor/vendor oversight.Strong working knowledge of HVAC or Clean Utilities (WFI, SIP, CIP etc) in a GMP environment.Experience working with automated documentation systems (e.g., Valgenesis, TIMs). If you would like to apply or find out more, get in touch now!#LI-CB1

CQ Engineer - Germany, Frankfurt - 18 Month 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: Ensure compliance with BS 7671, IEC standards, GMP, GEP, and project specifications.Witness electrical testing: continuity, insulation resistance, polarity, Zs, RCDs.Maintain GMP-compliant quality records (NCRs, CAPAs, test sheets, redlines).Monitor installation quality in cleanrooms, utility areas, and plant rooms.  What you’ll need: Degree or HNC/HND in Electrical Engineering.Experience in pharmaceutical or GMP-regulated construction projects.ISO 9001 or GMP training desirable.ECS/CSCS card; professional membership (IET/CQI) beneficial. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-CO1

CSA Engineer - Germany, Frankfurt - 18 Month ContractLooking 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 CSA 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: Oversee CSA aspects of cleanroom and HVAC installations during commissioning and qualification phases.Review and validate design documentation, specifications, and drawings for compliance with GMP, ISO, and project standards.Conduct field inspections and assessments of cleanroom finishes, architectural elements, and HVAC-related civil works.Collaborate with mechanical, electrical, and process teams to ensure integrated system performance.  What you’ll need: Bachelor’s degree in Civil, Structural, or Architectural Engineering (or related discipline).Extensive experience in CSA engineering within cleanroom/HVAC environments.Proven track record in commissioning and qualification in GMP-regulated industries.Strong understanding of cleanroom classifications (ISO 14644), airflow principles, and HVAC integration. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-CO1

QC Quality Systems Specialist - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a QC Quality Systems Specialist 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: Lead and manage QC Investigations assignedFacilitate root cause analysis and problem solving sessionsComplete the generation of associated investigation reportsDetermine and create CAPA’s, Effectiveness Reviews, and Supplemental Tasks as requiredPresent investigations at IRB to senior management What you’ll need: Proficiency in communication and collaboration at a variety of levelsProven success working well in a team environment with flexibility to react to changing business needsDemonstrated problem solving, project management abilityExcellent time management and organisational skillsExcellent technical writing skills If this role is of interest, please apply now!#LI-JS4

Electrical Maintenance Technician - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for an Electrical Maintenance Technician 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: Work Safely – identify risks and put in place mitigation actions if required.Ensure that equipment failures or issues are responded to promptly and appropriately in a cross functional environment.Record interventions including failure codes. Provide guidance and solutions for preventative action where required.Execute planned maintenance routines including predictive, preventative and calibration activities. What you’ll need: The successful candidate must possess at minimum a Level 6 Electrical qualifications or an electrical apprenticeship.Extensive experience in a maintenance or relevant engineering role in a regulated manufacturing environment.Experience in a regulated biopharmaceutical, pharmaceutical, medical device, facilities maintenance or FMCG facility is required.High level of attention to detail in following procedures and must be flexible and open to change.GMP experience. If this role is of interest, please apply now!#LI-AJ1

API Plant Technologist - Ireland, Dublin - 6 Month ContractOur client is one of the world’s largest pharmaceutical organisations. With continued organisational growth including ongoing investment across the portfolio and capital projects programme at their manufacturing facility in Dublin, an excellent opportunity has arisen for a API Plant Technologist to join the team. What you'll do: Perform duties as directed in whatever area of manufacturing operations they are currently assigned. This would include (but not be limited to) batch processing, utility monitoring and waste management.Assist in training of API team members with on the floor activities.Work with API Plant Team Lead and engineers to complete scheduling for batch productionAssist in the development of Standard Operating Procedures (SOPs) and Batch Manufacturing Records. What you'll need: Extensive experience in s similar roleExperience in an API manufacturing facility would be an advantage.Experience in a team lead role would be an advantage.Experience handling and working with hazardous chemicals would be essential. For more information on this position, please apply with a copy of your CV today!#LI-CB1

Senior CQV Engineer - Denmark, Copenhagen - 12 Months Initial Contract Our 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 Senior CQV Engineer to join their team in Copenhagen.What you'll do: Coordinate Mechanical Completions Line Walks, ensuring readiness for commissioning.Oversee the development and execution of IQ/OQ/PQ protocols, ensuring compliance with GMP and regulatory standards (FDA, EMA, MHRA).Facilitate daily board meetings, providing clear updates on progress, risks, and mitigation strategies.Collaborate with cross-functional teams (Engineering, QA, Operations) to ensure seamless system integration.Manage project documentation, including qualification reports, deviation logs, and risk assessments. What you'll need: Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical) or Life Sciences.Advanced degrees or certifications (e.g., PMP, Lean Six Sigma) are a plus.Extensive experience in commissioning and qualification, preferably in biopharma or regulated industries.Proven experience in leading large-scale projects, including planning, execution, and delivery.Strong understanding of commissioning of Clean & Black utilities.Familiarity with GMP, GEP, FDA, and EU regulations. If this role is of interest, apply now!#LI-DC1