Information Scientist

CSV Engineer - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for 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

CQV Lead (Facility HVAC EM BMS) - Denmark, Copenhagen - 12 Months Initial ContractOur client, a global pharmaceutical company, are looking for a CQV Lead 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: Provide input and guidance for planned CQV activities related to federated scheduleParticipate in Facility (HVAC EM BMS) schedule and planning activities to support and amend existing scheduleReview and participate in planned equipment and system walk downs and SATGive oversight, guidance, and support in application of governance and expectationsEnsuring that Commissioning, Qualification, and Validation (CQV) activities meet project and regulatory requirements What you'll need: Strong Process Background within API ManufacturingPharma Experience and background is essentialRelevant experience in required fieldExperience of working in a cross-functional team If you would like to apply or find out more, get in touch now!#LI-LH1

CQV Lead (Black Utilities) - Denmark, Copenhagen - 12 Months Initial Contract Our client, a global pharmaceutical company, are looking for a CQV Lead 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: Provide input and guidance for planned CQV activities related to federated scheduleParticipate in Black Utilities schedule and planning activities to support and amend existing scheduleReview and participate in planned equipment and system walk downs and SATGive oversight, guidance, and support in application of governance and expectationsEnsuring that Commissioning, Qualification, and Validation (CQV) activities meet project and regulatory requirements What you'll need: Extensive industry experienceStrong Process Background within API ManufacturingPharma Experience and background is essentialClient experience with skills in creating and reviewing procedures and strategy. If you would like to apply or find out more, get in touch now!#LI-LH1

CQ Lead (Electrical & Instrumentation) - Denmark, Copenhagen - 12 Months Initial ContractOur client, a global pharmaceutical company, are looking for a CQ Lead 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: Provide input and guidance for planned CQV activities related to federated scheduleParticipate in E&I schedule and planning activities to support and amend existing scheduleReview and participate in planned equipment and system walk downs and SATGive oversight, guidance, and support in application of governance and expectations What you'll need: Extensive industry experience Strong Process Background within API ManufacturingPharma Experience and background is essentialExperience of working in a cross-functional team If you would like to apply or find out more, get in touch now!#LI-LH1

Senior Validation Engineer - US, Seattle - 4 Months Initial ContractOur client, a global biotechnology organisation, is recruiting for a Senior Validation Engineer to join their capital project in Seattle. This new build facility will house a therapeutic protein production plant, and we are looking for a Senior Validation Engineer to help expand our client's biotech operations throughout Europe. As the Senior Validation Engineer you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.What you’ll do: Lead the planning, development, and execution of EMPQ protocols (IQ/OQ/PQ) for new and existing equipment, utilities, and process systems.Write clear, compliant, and technically robust EMPQ protocols aligned with GMP, GAMP 5, and site validation master plans.Execute EMPQ protocols on the manufacturing floor, ensuring accurate data capture and adherence to safety and GMP requirements.Ensure validation activities comply with FDA, MHRA, EU Annex 15, and other applicable regulatory frameworks.Partner with Engineering, Facilities, Manufacturing, Quality Assurance, and external vendors to ensure equipment readiness and qualification success. What you’ll need: Bachelor’s degree in Engineering, Life Sciences, or related technical discipline.Extensive experience in validation within GMP-regulated industries (pharmaceutical, biotech, medical devices, or similar).Proven expertise in EMPQ, including authoring and executing IQ/OQ/PQ protocols.Strong understanding of regulatory requirements: FDA 21 CFR Parts 210/211, EU GMP, Annex 15, GAMP 5.Exceptional technical writing skills and ability to produce clear, audit-ready documentation. If this role is of interest, please apply now!#LI-CO1

Validation Engineer - US, Seattle - 4 Months Initial ContractOur client, a global biotechnology organisation, is recruiting for a Validation Engineer to join their capital project in Seattle. This new build facility will house a therapeutic protein production plant, and we are looking for a Validation Engineer to help expand our client's biotech operations throughout Europe. As the Validation Engineer you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.What you’ll do: Plan, develop, and execute qualification activities (URS, RA, IQ/OQ/PQ) for QC laboratory instruments and systems.Author clear, compliant qualification protocols and reports for QC equipment.Maintain qualification status throughout the equipment lifecycle, including periodic reviews, requalification, and retirement.Ensure QC equipment qualification meets regulatory requirements (FDA, MHRA, EU GMP, Annex 15).Work closely with QC analysts, QA, Engineering, IT, and vendors to ensure equipment readiness and compliance. What you’ll need: Bachelor’s degree in Engineering, Life Sciences, Chemistry, or related technical field.Experience in a GMP-regulated QC laboratory environment (pharmaceutical, biotech, ATMP, or medical devices).Hands-on experience with QC equipment qualification (IQ/OQ/PQ).Strong understanding of analytical laboratory instruments (e.g., HPLC, GC, UV-Vis, PCR, balances, incubators).Excellent technical writing and documentation skills. If this role is of interest, please apply now!#LI-CO1

QA/QC Welding Inspector - Denmark, Copenhagen - 12 Month Contract  Our client, a global pharmaceutical company, are looking for a QA/QC Welding Inspector 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: Verify piping fabrication and installation against approved isometrics, P&IDs, weld maps, material specifications, and project standardsInspect welding activities including fit-up, root pass, hot pass, fill and cap ensuring adherence to specificationReview and approve and amend welding documentationConduct visual weld inspections (VT) and coordinate NDT activities (RT, PT, MT, UT) with third-party inspectors, including the EPCMMonitor weld traceability ensuring full linkage between welds, materials, NDT results, and turnover documentation What you'll need: Strong knowledge of welding processes (GTAW, SMAW, GMAW, orbital welding).Ability to interpret WPS, PQR, WPQ, weld maps, and consumable requirements.Skilled in visual weld inspection (VT) and coordination of NDT (RT, PT, MT, UT).Understanding of material traceability, heat numbers, MTRs, and stainless-steel handling.Mechanical Engineering (degree or diploma). If you would like to apply or find out more, get in touch now!#LI-LH1

Senior Scientist - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Senior 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: Provide technical oversight and ownership of analytical methods. This includes partnering with analytical development to ensure method readiness for validation, assisting with validation protocols, gathering data generated by analytical development/QC labs and assisting with validation reports.Lead complex projects and lead a team of scientists to meet deadlines and collaborate with key stakeholder groups.Provide technical oversight of method revisions.Lead method transfers to QC GMP labs within and outside of the company. What you’ll need: Specific Knowledge, Skills, Abilities, etc:Demonstrated trouble shooting and hands on experience with protein separation methods, for example, CE_SDS or iCIEF Electrophoresis, HPLC and UPLC Chromatography including Size-Exclusion chromatography, ion exchange and UVIS spectroscopy based technologies.Good understanding of the fundamentals of protein characterisation methods such as peptide mapping, and carbohydrate analysis.Experience leading complex projects, projects teams and meeting tight deadlines If this role is of interest, please apply now!#LI-JS4

Validation Engineer - Redmond, Seattle - 4-6 Month ContractOur client, a global biotechnology organisation, is recruiting for a Validation Engineer to join their capital project in Redmond. This new build facility will house a therapeutic protein production plant, and we are looking for a Validation Engineer to help expand our client's biotech operations throughout Europe. As the Validation Engineer you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.What you’ll do: Identify gaps, risks, and improvement opportunities, escalating issues where required.Support the maintenance of validated status through impact assessments, requalification planning, and validation updates.Maintain validation files and ensure documentation is audit-ready at all times.Participate in internal and external audits, providing subject-matter expertise on validation lifecycle and periodic review processes. What you’ll need: Experience in pharmaceutical, biotech, or other regulated GMP environments.Strong understanding of validation principles (IQ/OQ/PQ), equipment qualification, and process validation.Familiarity with regulatory guidelines including EU GMP Annex 15, FDA 21 CFR Parts 210/211, and data integrity expectations.Excellent analytical and documentation skills with a high attention to detail. If this role is of interest, please apply now!#LI-CH3