Devon Spelman-Glasford

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, North Carolina - 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 North Carolina 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

Procurement Assistant - US, Ohio - 12 Month Contract Be 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 Procurement Assistant to join the team and help deliver this world-class program. What you’ll do: Support the Capital Procurement team in executing procurement activities aligned with the ProjectProcurement Plan and Global Capital Facility Project plans.Manage a high volume of purchase requisitions concurrently (often 10 active requisitions), prioritising workload effectively.Proactively acknowledge receipt of requisitions and provide regular status updates to requisitioners without prompting.Source capital equipment and services, analyse supplier quotations, and prepare commercial bid analyses with recommendations. What you’ll need: Degree or qualification in Business, Supply Chain, Procurement, or equivalent experience.Extensive experience in a buyer, procurement assistant, or purchasing role.Hands-on experience using SAP (including MRP) and/or Ariba for purchasing activities.Experience supporting capital projects or large-scale industrial environments preferred. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Senior Project Manager - UK, Surrey - 12 Month ContractWe are looking for an experienced Senior Project Manager for a fantastic 12 month contract based in Surrey.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: Lead the programme from initial definition through planning, delivery, commissioning, and handover.Hold accountability for final engineering aspects, ensuring design intent, technical standards, safety requirements, and compliance obligations are met.Understand and oversee the full commissioning process for R&D and laboratory environments, ensuring readiness for functional testing, validation, and operational ramp-up.Develop and maintain integrated programme schedules, resource plans, and performance baselines. What you’ll  need: Extensive experience managing major capital programmes, ideally within R&D, laboratories, scientific facilities, pharma, defence, advanced engineering, or highly regulated technical environments.Strong understanding of engineering processes, design assurance, and technical governance.Demonstrable exposure to commissioning activities within complex facilities.Proven ability to lead multidisciplinary teams through full lifecycle delivery If this role is of interest to you, please apply now!#LI-TN1

Process & Piping Integration Lead - 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 Process & Piping Integration Lead to join the team and help deliver this world-class program. What you’ll do: Lead owner-side integration of process, piping, and equipment engineering scopes.Coordinate closely with the Owner Equipment Manager on equipment data, layouts, and installation requirements.Transition from design integration to discipline-focused construction support.Ensure piping and equipment systems are designed for cleanability, testability, and access. What you’ll need: Extensive experience in pharma, biotech, or complex regulated projects.Strong background in process systems, piping engineering, and equipment integration.Experience working with EPC delivery models and owner-side teams.Solid understanding of system-based turnover and CQV execution. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Process Utilities Integration Lead - 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 Process Utilities Integration Lead to join the team and help deliver this world-class program. What you’ll do: Integrate clean and dirty utility systems including WFI, PW, clean steam, process gases, HVAC utilities, chilled water, steam, condensate, waste, and drains.Challenge EPC utility designs for operability, maintainability, and sequencing.Support installation sequencing, testing, flushing, passivation, and startup activities.Ensure utility systems meet CQV access, testing, and documentation requirements. What you’ll need: Extensive experience in clean utilities and facility infrastructure for regulated projects.Strong understanding of utility system commissioning and CQV expectations.Experience working with EPCs and owner teams.Utility systems are turned over aligned with process and CQV schedules. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1