Snr I&C Engineer

Procurement Director - 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 Procurement Director to join the team and help deliver this world-class program. What you’ll do: Own and execute the end-to-end procurement strategy for a $1bn greenfield pharmaceutical manufacturing project.Work closely with construction leadership to ensure procurement decisions directly support buildability, logistics, and site execution.Lead high-value negotiations with EPCMs, construction contractors, and major equipment suppliers.Oversee procurement of complex pharmaceutical process equipment and supporting utility systems. What you’ll need: Bachelor’s degree in Engineering, Construction Management, Procurement, Supply Chain, or related discipline (Master’s degree or MBA preferred but not required)Extensive experience leading procurement on large-scale capital projects ($500m ), ideally $1bn greenfield builds.Strong construction acumen with a practical understanding of how procurement decisions impact site execution.Demonstrated experience working with S-curves, cash flow forecasting, and procurement phasing aligned to construction schedules. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

HSE Data Analytics Lead - US, Remote - 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 HSE Data Analytics Lead to join the team and help deliver this world-class program. What you’ll do: Responsibilities include collecting, cleansing, and validating data from various sources and projects.The professional translates operational HSE data into meaningful metrics for improved HSE outcomes.Tasks involve performing trend analysis, frequency and severity analysis, and improvement effective.Identify high-risk trends, recurrent failure points, and weak signals that may precede LIFE incident, supporting risk mitigation efforts.  What you’ll need: Extensive Experience In data analyticsExperience in Safety or worker compensation insurance actuarial servicesExperience in Rote Cause AnalysisBachelor’s degree or advance technical studies on statistics, actuarial science or engineering Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

CQ Engineer Isolator - Germany, Frankfurt - 12 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 Isolator 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: Lead the development and optimization of Vaporized Hydrogen Peroxide (VPHP) decontamination cycles for Material Transfer Isolators and Sterile Test Isolators, ensuring compliance with aseptic processing standards and regulatory requirements.Conduct smoke studies to assess airflow patterns and contamination control during isolator interventions. Supported Environmental Monitoring Performance Qualification (EMPQ) activities to validate cleanroom and isolator environments.Experienced in the strategic placement, retrieval, and interpretation of Biological Indicators (BIs) during VPHP cycle development to verify sterilization efficacy. What you’ll need: Bachelor’s degree in Engineering, Life Sciences, or related fieldExperience in CQV within pharma or biotechProficiency in writing and executing qualification protocolsFamiliarity with electronic documentation systems and validation lifecycle Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-CO1

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

Procurement Equipment Advisor - 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 Procurement Equipment Advisor to join the team and help deliver this world-class program. What you’ll do: Own post-award execution of major process and utility equipment purchase orders.Actively expedite equipment suppliers, holding them accountable to fabrication schedules, inspection points, FAT readiness, and delivery commitments.Maintain direct, routine communication with vendors to identify and mitigate delivery risk early.Track supplier progress against contractual milestones, manufacturing schedules, and project needs.Challenge supplier recovery plans and escalate issues where schedule, quality, or documentation is at risk.  What you’ll need: Extensive experience buying and executing pharmaceutical manufacturing equipment on CAPEX projects.Proven track record managing long-lead equipment suppliers through fabrication, FAT, shipment, and delivery.Strong understanding of GMP equipment manufacturing, inspection, and release processes.Experience expediting vendors and applying commercial and schedule pressure.  Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

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!