Procurement Equipment Advisor

Commissioning Lead - UK, Surrey - 12 Month ContractWe are looking for an experienced Commissioning Lead 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: Develop and own the Commissioning Strategy, Commissioning Plan, and Master Commissioning Schedule.Lead commissioning meetings and workshops with contractors, design teams, and stakeholders.Ensure commissioning documentation is produced, reviewed, and approved.Ensure commissioning activities are executed safely, with appropriate risk assessments and method statements.Support training programmes for operational staff, ensuring knowledge transfer. What you’ll  need: Proven experience as a Commissioning Lead/Manager on complex construction projects.Experience delivering commissioning for laboratories, R&D facilities, or highly serviced technical environments.Strong understanding of building systems, MEP design, automation controls, and specialist lab systems.Ability to interpret technical drawings, specifications, and commissioning protocols.Excellent leadership skills with the ability to influence across multiple stakeholders. If this role is of interest to you, please apply now! #LI-TN1

Spare Parts / Materials Assistant - US, North Carolina - 12 Month ContractOur client, a global pharmaceutical manufacturing organization are looking for a talented Spare Parts / Materials Assistant to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States. What you'll do: Work with construction, startup, and commissioning teams to identify, catalog, and track required spare parts and critical materials for new equipment.Assist with developing Scope of Work (SOW) documents for vendor-supplied parts, pursuing RFPs, and clarifying technical questions between vendors and engineering teams.Assist with vendor onboarding, specifically focusing on the logistics of material delivery, storage, and handling.Follow up on material submittals, vendor document control, and send reminders to responsible parties to ensure parts arrive to support commissioning schedules. What you'll need: Degree preferred but not required; Certification in project management or a related field.Extensive experience in materials management, spare parts coordination, or similar assistant manager role.Extensive experience in pharmaceuticals, biotechnologies, or similar regulated industry.Extensive experience with procurement processes, such as PO creation, RFPs, and basic material tracking. If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Vendor Management Assistant - US, North Carolina - Long Term ContractOur client, a global pharmaceutical manufacturing organization are looking for a talented Vendor Management Assistant to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States. What you'll do: Work with startup, commissioning, qualification teams to understand needs for upcoming Vendor ServicesAssist with developing SOW’s, pursuing RFP’s, clarifying questions between Vendor and service requestorsAssist with Vendor onboarding steps alongside Safety and Procurement counterpartsFollow up on paperwork submittals, and send reminders to responsible parties when action is required What you'll need: Proficient communicator, with ability to understand status of activities, quickly and effectively relay to other team members both written and verballyExtensive experience in construction management or similar assistant manager type roleExtensive experience in pharmaceuticals, biotechnologies, biomedical or similar fieldExtensive experience with general procurement processes, such as RFPs, SOWs, PO’s and basic management of cost, scope, and schedule If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Program Manager - UK, Surrey - 12 Month ContractWe are looking for an experienced Program 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-JS4

EHS Project Engineer - Ireland, Dublin - 12 Month 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 EHS Project Engineer. What you'll do: Ensure compliance with EHS regulations including HSA and EPA.Develop and maintain assigned EHS programs and provide support for other programmes.Deliver technical EHS training to projects, engineering, operations, and laboratory staffMaintain EHS documentation including risk assessments, SOPs, and change control records.Collaborate with Engineering, Quality, and Operations to ensure alignment on EHS goals. What you'll need: Bachelor’s degree in Environmental Engineering, Chemical Engineering, Occupational Safety, Industrial Hygiene, or a related technical discipline.Extensive EHS experience in pharmaceutical, biotech, medical device or chemical manufacturing environments supporting projects/operations.Proven experience supporting capital projects, facility upgrades, and equipment installations with EHS integration.Demonstrated involvement in GMP-regulated operations and cleanroom environments.Proficient with Construction Safety and associated regulations and requirements. If this role is of interest to you, please apply now!

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 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, Raleigh - 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 Raleigh, NC 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