Leading life sciences recruitment for pharmaceuticals and biotech

QA Compliance and Systems Specialist – Dublin – Pharmaceuticals One of the top 10 best companies to work in Ireland is looking for QA Compliance and Systems Specialist 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: Preparation, review and approval of Material Qualification Documentation.QA disposition of raw materials, level 1 & level 2 consumables.Authoring, review and approval of QA-related procedures.QA review, assessment and approval activities for Biologics Manufacture, as applicableBe a core team member of the QA Compliance Materials Management team engaging in other support activities as required. What you’ll need: BSc in Science or related discipline with QA or related experience in a Biologics or Pharmaceutical environmentA clear understanding of cGMP requirements for manufacturing and/or systems and complianceKnowledge of material qualification & SAP would be a distinct advantage.Required to work on his/her own initiative in addition to working as part of a team. Must be able to work across a team matrix to meet accelerated timelines. If this role is of interest, please apply now! #LI-JS4

QA Senior Specialist – Dublin – Pharmaceuticals One of the top 10 best companies to work in Ireland is looking for QA Senior Specialist 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: Support the Qualified Person with the Batch Certification functionPrepare and review batch documentation packages for QP release as per SOP requirementsLiaise with the Supply Chain and Quality colleagues to ensure that disposition lead times are consistently metUpdate SOPs, controlled documents i.e. FORMS and OJTsAssist in new product introduction activities as requiredProvide training to new team members What you’ll need: A degree in science, engineering or related discipline is essential. Experience in pharmaceutical /biopharmaceutical industryExperience using data or electronic document management systems (DCA, Trackwise, Infinity, and SAP)Strong working knowledge of Microsoft Excel and PowerPointAbility to work on his/her own initiative in addition to working as part of a team If this role is of interest, please apply now! #LI-JS4

CQV Engineer – Massachusetts – Pharmaceuticals – Contract Our client is a leading American multinational CDMO specializing in the development and manufacturing of complex, highly regulated active pharmaceutical ingredients (APIs). Our client is seeking an experienced CQV/Validation Engineer to contribute to an exciting project in the New England area. What you’ll do: Generate, execute, review, finalize, and approve validation/qualification protocols and reportsManage and update project validation plans for specific projectsAssist and deliver amendments to the qualification(s) to ensure qualification compliance within agreed upon timelines.Utilize computerized asset management system for managing validation/qualification schedulesGenerate operational and maintenance SOPs, FATs, URSs, FRSs, validation protocols and reports What you’ll need: Bachelor’s degree required; B.S. in engineering preferred.Experience in an Engineering or a closely related role in a manufacturing or R&D environment.Experience in a GMP environment required. Experience in the pharmaceutical/API/chemical manufacturing industry preferred.Experience in a Validation Engineering role generating and executing Commissioning, Installation Qualification (IQ), Operation Qualification (OQ), and Performance Qualification (PQ) protocols If you are interested, please apply now for immediate consideration and further information. #LI-BP1

QC Microbiology Specialist – Dublin – Pharmaceuticals – 11-month contract Do 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 QC Microbiology Specialist. What you’ll do: Perform and support QC analytical activities including in-process, release and stability related testing.Provide day to day direction and scheduling to the QC analyst team.Responsible for the qualification, maintenance, and/or integration of the QC methods, in compliance with up-to-date data integrity, regulatory, and industry standards.Responsible for driving a culture of Continuous Improvement.Ensure that cGMP standards are maintained at all times.Accountable for change control process and mechanisms required to maintain a state of continued compliance for the methods.Manage deviations, CAPAs and change controls. What you’ll need: Industry experience with significant knowledge and experience working in a Microbiology Laboratory in a pharmaceutical companyExperienced in testing as per the pharmacopeia’sWorking knowledge of QC Digital Systems (eLogs, Electronic Lab Notebook, LIMS etc.)Ability to respond to changing prioritiesStrong organisational skills If this role is of interest to you, please apply now! #LI-JS5

Chapter Engineer OT Shopfloor & Cyber Security – Dublin – Contract – Pharmaceuticals Our client is one of the world’s largest pharmaceutical organisations. With continued organisational growth including ongoing investment across the portfolio and capital projects programme at their manufacturing facility in Ireland, an excellent opportunity has arisen for a Chapter Engineer OT Shopfloor & Cyber Security to join the team. What you’ll do: Operates CIM OT Shopfloor Endpoint Services needed to publish shopfloor applications on GMSGQ sites, following global CIM standards and procedures.Represents the CIM OT Shopfloor Endpoint & Cyber Security team at site and/or region, collaborating with local and global teams.Partners within DD&T and CIM chapters to support defining/evolving standards and site level deliveries.Holds interfacing service providers accountable withing the service operations processes.Runs continuous monitoring and improvement.Build & upgrade OT Shopfloor Endpoint & Cyber Security environments.Maintains the CIM OT Shopfloor asset inventory in CMDB. What you’ll need: Bachelor’s degree in Computer Science, Business Administration with focus manufacturing, or related field, or equivalent experience requiredProven and strong knowledge of networks, especially in the area of OT production and laboratory environmentsBackground in IT Service Management and Service DeliveryExperience in IT and OT Networking Experience in Cloud computing (AWS, Azure) is nice to have For more information on this position, please apply with a copy of your CV today! #LI-CB1

LOTO Coordinator - North Carolina – Pharmaceuticals Our client, a global pharmaceutical manufacturing organization are looking for a talented LOTO Coordinator 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: Execute and manage LOTO (Lockout/Tagout) procedures on electrical installations and equipmentHelp coordinating and documenting all LOTO activities across projects and operational environments on the electrical side.Assisting in operating the LOTO control office, including issuing, tracking, and closing LOTO permitsPhysically lock and isolate electrical panels, switchboards, MCCs, and distribution boardsAct as AP (Authorized Person) for electrical work and permittingSupport safe energization and de-energization during commissioning What you’ll need: Certified Electrician, Electrical Installer, or Electrical EngineerExperience with electrical LOTO procedures and safety lockout systemsBackground from pharmaceutical, biotech, or other regulated industries is a strong advantageFamiliarity with digital permit systems, or LOTO tracking platforms is a strong advantageUnderstanding of electrical safety regulations and site energy controlFluent in English, both spoken and written If you are interested, please apply now for immediate consideration and further information.

Process Technician - North Carolina – Pharmaceuticals Our client, a global pharmaceutical manufacturing organization are looking for a talented Process Technician 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. Essential Duties and Responsibilities for this role include, but are not limited to: Provide recommendations to develop preventative maintenance plans to minimize equipment downtimeContribute to Standard Operating Procedure (SOP) development and revisions for process maintenance related activitiesDiagnose and troubleshoots equipment malfunctionsAssist in the installation and commissioning of new equipmentMaintain accurate maintenance records and documentationFollo standard operating procedures (SOPs) to ensure compliance with safety and Good Manufacturing Practices (GMP) quality standards Requirements: Knowledge of mechanical, electrical, and control systemsKnowledge of GMP requirementsEffective communication, both written and oralAbility to work in a team environmentKnowledge of lean manufacturing principles If you are interested, please apply now for immediate consideration and further information.

Upstream Associate Scientist - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for an Upstream Associate Scientist 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: Support commercial and product technical transfers including late-stage process characterisation programs.Design and execution of experiments with an ability to interpret data in upstream cell culture to support NPI, process characterisation and site operations.Media preparation and development supporting lab and manufacturing upstream processes.Preparation of laboratory operating procedures, study protocols and reports. What you’ll need: An MSc. in Biological or Chemical Sciences/Engineering is preferred or BSc, extensive industry and/or academic experience.Practical knowledge of cell biology, protein expression, protein structure and function and experience with cell culture or fermentation laboratory activities.Candidates must possess good organisational skills and strong attention to detail.Demonstrates ability to troubleshoot, interpret and discuss data.  If this role is of interest, please apply now!#LI-JS4

Automation Project Manager - US, Ohio - 8 Month ContractThis is a fantastic opportunity for an Automation Project Manager  to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn. What you'll do: Lead planning, execution, and delivery of automation projects from initiation through completionCoordinate cross-functional teams including engineering, operations, and external vendorsManage project scope, timelines, budgets, and resources to ensure alignment with strategic goalsIdentify and mitigate risks, resolve issues, and maintain clear communication across stakeholders What you'll need: Proven experience in project management, ideally within automation or controls environmentsStrong understanding of industrial automation systems, PLCs, SCADA, or related technologiesExceptional organizational, communication, and leadership skillsAbility to manage multiple projects and priorities in a fast-paced setting If this role is of interest, please apply now! #LI-KS1