Supply Planner

I&C Metrology Engineer - US, North Carolina - 12 Month Initial ContractOur client, a global pharmaceutical manufacturing organization are looking for a talented I&C Metrology Engineer 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: Be part of a team of Metrology Specialists, Technicians, and Team Leads Supporting Aseptic and Finish Production areasSupporting calibrations across the site, including Formulation, Filling, QC, Facilities, Finish Production and Component Prep. The calibration program includes on-site and vendor performed calibrations.Supprt for all audit / inspection responsibilitiesDeviation and Change Control responsible (including SPS)Create and maintain department SOPs What you'll need: Bachelor’s degree in Engineering (Instrumentation & Controls, Electrical, Mechanical, or related discipline) or equivalent technical experience.Extensive experience in metrology, calibration, or instrumentation engineering within a GMP-regulated bio-pharmaceutical, medical device, or FDA-regulated manufacturing environment.Experience supporting drug substance manufacturing operations preferred.Strong knowledge of calibration and metrology principles for process, laboratory, and facility instrumentation. If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Procurement Manager - Spain, Madrid - 12 Months Initial ContractLooking to take your career to the next level? We’re recruiting for a high-impact pharmaceutical project located near Madrid. With major capital investment experience driving various facility build projects. This is a unique opportunity for a Procurement Manager 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: Analyse investment project requirements and define optimal purchasing strategies (make/buy, source, tender, negotiate).Manage the complete acquisition cycle for goods, installations, technologies, and specialized services: RFI/RFQ/RFP, supplier lists, bid comparison, contracting.Lead complex commercial and technical negotiations with national and international suppliers.Collaborate with technical teams and the Project Management Office to define specifications and evaluation criteria. What you’ll need: Expertise in procurement methodologies for complex CAPEX projects.Proficiency in tendering tools and main contractual frameworks (EPC, EPCM, framework agreements, supply and service contracts).Strong skills in economic analysis, cost modelling, and budgeting.Familiarity with engineering, construction, and commissioning processes (industrial, energy, manufacturing, or infrastructure sectors). Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-LH1

Quality Assurance Specialist/QP - Ireland, Sligo - 12 Month ContractLocated on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a Quality Assurance Specialist/QP to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow. What you’ll do: Comply with EudraLex Volume 4 EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use Annex 16: Certification by a Qualified Person and Batch Release; Article 47 of Directive 2001/83/EC.Qualified Person is responsible for ensuring that each individual batch has been manufactured and checked in compliance with laws in force.To ensure that products manufactured by the client are manufactured in accordance with the relevant GMPs.Responsible for the disposition of bulk product manufactured at site as acceptable for release or reject based on the information available relating to the manufacture and testing of the product. What you’ll need: Third level qualification in a science discipline with extensive experience in the pharmaceutical industry.MSc in Industrial Pharmaceutical Science or similar course recognised by Regulatory Authority to permit Qualified Person (QP) status as per Article 49 of Directive 2001/83/ECExtensive industrial experience gained in an FDA and EMEA approved pharmaceutical environment.Extensive experience gained within an aseptic processing environment, ideally gained within a quality function. If this role is of interest, please apply now!#LI-JS4

QC Material Management Analyst - Ireland, Dublin - 12 Month ContractLocated on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a QC Material Management Analyst to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow. What you’ll do: Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.Liaise with Engineering Stores to ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.Manage TempTales and shipping documents when receiving samples from external sites. What you’ll need: The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team based collaborative environment.The ideal candidate should hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline.Extensive experience in a pharmaceutical / healthcare laboratory or related technical function. If this role is of interest, please apply now!#LI-JS4

Automation Area 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 Automation Area Lead to join the team and help deliver this world-class program. What you’ll do: Technical ownership for an area in a projectDefine the S88 software structure and list for the areaDevelop draft function design specifications for the areaWork with system integrators to finalize the functional specificationsParticipate in P&ID and control strategy reviews What you’ll need: Key Measures of Success:Area automation deliverables consistent with program standards and philosophy.FDS and software deliverables delivered on time and to quality.Issues tracked, resolved, and documented with minimal impact to schedule. Area automation scope delivered successfully through design, FAT, SAT, and turnover. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Laboratory Systems Specialist - Dublin, Ireland - 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 Laboratory Systems Specialist. Essential Duties and Responsibilities for this role include, but are not limited to, the following: The motivation to be an inspiring member of a high performing team.The desire to continuously learn, improve and develop.Be the SME on data management systems for instrument control in the laboratories, this includes but is not limited to GLIMS (Global Labware LIMS Platform), Laboratory Execution Systems (LES), Lonza MODA and Waters Empower.Work within an environment of right first time in everything that we do, through a focus on principles of lean, including simplification, standard work, visual management Desirable Experience: Degree qualification in a Technical discipline.Extensive experience in laboratory systems, Labware LIMS experience preferred.Previous experience with configuring, building, maintaining laboratory management systems such as LIMS/ MODA and /or Empower systems and interest in coding/ script.Ability to think logically and be proactive under pressure. If this role is of interest to you, please apply now!#LI-CH3

Contracts Manager - 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 Contracts Manager to join the team and help deliver this world-class program. What you’ll do: Lead the administration and governance of construction contracts during executionOwn the full contract lifecycle post-awardAct as the primary commercial and contractual interfaceSupport dispute resolution and claims management  What you’ll need: Extensive experience of contract management experience on large-scale CAPEX projects ($250m )Owner’s representative or EPCM delivery modelsConstruction-phase contract administration Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Project Manager - US, North Carolina - Long Term ContractOur client, a global pharmaceutical manufacturing organization are looking for a talented Project Manager 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: Lead the planning, execution, and delivery of capital projects, ensuring alignment with business objectives, schedule, and budget.Develop and manage project scopes, budgets, schedules, and risk assessments, driving accountability across teams.Coordinate with cross-functional stakeholders, including engineering, operations, quality, procurement, and regulatory teams, to ensure seamless project execution.Manage contractor and vendor relationships, overseeing procurement, contract negotiations, and project execution. What you'll need: Extensive experience in capital project management within the pharmaceutical, biotech, or life sciences industry.Proven track record of delivering complex capital projects on time and within budget.Experience managing process equipment, utilities, automation systems, and facility expansions.Strong leadership and communication skills (written and verbal), with the ability to influence, negotiate, and build relationships with stakeholders at all levels. If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Automation Engineer - Ireland, Dublin - 12 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 Automation Engineer. What you'll do: Partner with local site project teams to scope changes on the PLC systemMaintain Inventory and control upgrades to PLC/SCADA systemsFollow the SDLC Procedure to implement changes (covering RS updates, RTM Change control, Implementation and test)Assist in integrating PLC/SCADA systems to core systems on the Manufacturing network including the site historian, Time server, central software repository etc. What you'll need: Experience in the commissioning of PLC/SCADA systems at a GMP manufacturing site.Experience with Siemens software including TIA Portal, WinCC, PM-Analyse, Simatic LogonExperience interfacing to control systems via common industrial protocols such as OPC UA, Profibus, Profinet, MODBUS (RTU and TCP) If this role is of interest to you, please apply now!#LI-WS1