Explore opportunities for validation engineers

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

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

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

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

Cleaning Validation Engineer - Dublin, Ireland - 12 Months Initial ContractOne of the top 10 best companies to work in Ireland is looking for a cleaning validation 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: Performing all aspects of cleaning sampling required for cleaning validation for a new product.Activities include swab and rinse sampling, sample preparation, LIMS administration, submission to QC for analysis, correlation of QC results with cleaning change over protocols/ cleaning logbooks.Supporting product changeover activities.Assisting with LOTO (lockout/ Tagout) activities where required.Generation of standardized cleaning validation ECPs (Energy Control Plans). What you’ll need: A minimum of a BS qualification (Degree) in a scientific, technical or engineering discipline.Previous cleaning validation experience is an advantage.The ideal candidate would have biopharmaceutical Process / Validation knowledge.Exposure to cGMP in a fast-paced environment is required.Previous experience in working in a drug product filling facility would be advantageous. If this role is of interest, please apply now!#LI-JS4

Process Validation Specialist - Oxfordshire, UK - 12 Month ContractAre you a Process Validation Specialist professional with experience in Cell & Gene therapy? Are you looking to take the next step in your career and be part of an exciting new project? Then the position of process validation specialist is exactly what you’re looking for. This is your chance to work for a company that is a pioneer in gene and cell therapy focussing on long-term curative treatments. With vast investment being made into the organisation and new build projects on the horizon this is the ideal time to join the team and establish yourself as a key team member. Led by an experienced executive team, this is a fantastic opportunity to work for a high-profile Biopharma client. Essential Duties and Responsibilities for this x role include, but are not limited to, the following: Lead and execute process validation activities for cell and gene therapy manufacturing processes.Develop and author process validation documentationConduct ancillary validation studies (e.g., hold time validation, mixing studies, sterile filter validation).Ensure compliance with regulatory requirements for process validation and PPQ.Collaborate with cross-functional teams to support process characterization and control strategy development. Desirable Experience: Proven track record in process validation and process performance qualification (PPQ) within GMP manufacturing environments.Hands-on experience authoring validation documentation.Familiarity with regulatory requirements for process validation.Experience conducting ancillary validation studies).Prior exposure to cell & gene therapy or biologics preferred; small molecule experience acceptable. #LI-JM1

QA Validation Engineer - North Carolina, United States - 9-months contractOur client works across regulated sectors to build robust, repeatable compliance and validation practices. They prioritise clear guidance, clean documentation, and controls that fit how teams operate.  What you’ll do: The QA Validation Specialist is responsible for implementing, executing, and assessing quality systems, procedures, and records to support compliant GMP operations.The role works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation teams.Provide hands‑on QA support and oversight to internal teams and suppliers/contractors to ensure compliance with applicable quality standards, regulatory requirements, and industry guidance.Review and approve commissioning, qualification, and validation documentation.Review and approve qualification and validation deviations and discrepancies, supporting investigation and corrective actions.Work collaboratively across site functions to instil a strong quality culture, coaching in the application of GMP principles and the rationale behind them.Author, review, and approve controlled documents for Quality and other GMP functions, including SOPs, specifications, protocols, and reports.Assist in the preparation for, and hosting of, regulatory inspections and audits as required. What you’ll need: Degree in biological, physical or chemical sciences, engineering, or a related field, with  experience in QA within biologics manufacturing. Strong knowledge of risk‑based approaches to qualification and validation in a biotech quality environment.Hands‑on experience with qualification and validation of process equipment, isolators, bioreactors, clean utilities, automation systems, sterile filling, and cleanroom facilities.Solid understanding of relevant regulations and guidelines, including US and EU frameworks (e.g. FDA, EMA), ICH guidance, and industry best practice.Proven track record of working in a fast‑paced team environment, meeting deadlines, and prioritising work across multiple projects.Strong analytical and communication skills, sound judgement, and the ability to work effectively with colleagues and stakeholders.Excellent problem‑solving capability, with experience in root‑cause investigation and CAPA determination. If this roles is of interest to you, apply today!

DTI Validation Lead - US, North Carolina - 12 Months Initial ContractOur client, a globally recognized pioneer in Biotechnology, are recruiting for the position of DTI Validation Lead. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to join them on their global mission to better the lives of those effected by disease and illness. The project at hand is for the construction of a new build biomanufacturing plant based located on the East Coast. What you'll do: Develop and own the validation strategy for digital technology systems (e.g., MES, DCS/SCADA, Historian, lab systems, asset management tools, and digital workflow platforms).Lead CSV (Computer System Validation) planning and execution.Collaborate with engineering, automation, IT, quality, and construction teams to ensure integration and data flow meet compliance and data integrity standards.Ensure validation deliverables (URS, FS/DS, IQ/OQ/PQ, risk assessments, etc.) are created, reviewed, and approved per project timelines. What you'll need: Extensive experience in CSV/automation/IT validation within pharmaceutical or biotech manufacturing.Experience supporting greenfield/brownfield CAPEX projects highly preferred.Strong knowledge of GAMP 5, Data Integrity principles (ALCOA ), and GMP regulations.Proven leadership in cross-functional environments and vendor/contractor management. If this role is of interest, please apply now. #LI-DA1