Senior Embedded Software Engineer

Warehouse JIT & Outbound Logistics Process Associate - 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 Logistics Process Associate to join the team and help deliver this world-class program. What you’ll do: Design, build, and optimize material kitting workflows to ensure accurate, efficient transfer of materials from the central warehouse to manufacturing nodes.Collaborate with cross-functional teams to align kitting and transfer processes with manufacturing schedules and requirements while accounting for storage space within the manufacturing nodes JIT warehouses.Develop and document standard operating procedures (SOPs) and work instructions for kitting and transfer activities.Support Commissioning, Qualification, and Validation (CQV) activities for new or modified warehouse processes, equipment, and systems. What you’ll need: Bachelor’s degree in Engineering, Supply Chain, or related field.Experience in GMP-regulated environments, warehouse kitting, material transfer, and outbound logistics.Familiarity with CQV processes and documentation.Proficiency in SAP/EWM and familiarity with MES systems.Extensive experience in supervising or designing logistics operations, specifically the flow of materials through multiple process steps. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-KS1

Project Manager, Peptide Headblocks - 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 Project Manager to join the team and help deliver this world-class program. What you’ll do: Manage and oversee design and construction of the Peptides Headblock projects, ensuring completion on time, within budget, and to quality standards.Operate as the Owner’s Representative, ensuring alignment with project vision and requirements.Provide feedback on change orders, ensuring modifications are necessary, cost-effective, and maintain project integrity.Participate as part of the project team, managing stakeholders including Operations, C&Q, Design, Quality, Design-Build Partners, EPCM, and others as appropriate. What you’ll need: Strong problem-solving skills in project and program management.Excellent verbal and written communication skills.Extensive experience on relevant construction projects.Significant leadership experience with design and construction projects Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-KS1

Mechanical & Plumbing Quality 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 Mechanical & Plumbing Quality Manager to join the team and help deliver this world-class program. What you’ll do: Perform daily walkdowns of mechanical and plumbing systems, with emphasis on process piping and HVAC.Monitor installation quality of contractors, especially less sophisticated mechanical subcontractors, ensuring compliance with specifications.Review and interpret drawings and specifications to verify installation accuracy.Document findings through formal reports, NCRs (Non-Conformance Reports), and checklists. What you’ll need: Extensive mechanical/plumbing quality management in large ground-up construction projects.Strong background in process piping (highest priority system).Extensive understanding of HVAC systems, including quality walks and specification compliance.Ability to read and interpret specs and drawings accurately. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-KS1

Procurement Assistant - Denmark, Copenhagen - 12 Month ContractOur client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Procurement Assistant to join their new and exciting large-scale CAPEX investment programme. With a mission to provide process development and cGMP production in cell culture, microbial fermentation, and gene therapies, this is an outstanding opportunity make a genuine contribution to the biopharmaceutical industry. What you’ll do:Procurement of: Produce spare partsService agreementsRaw materialsToolsThe entire basic procurement processFollow up on delivery. What you’ll need: Strong procurement experienceStructure and know how to follow proceduresIs happy to be part of an ever changing project environmentCan do mentalitySelf-driven but not afraid to ask when in doubt If this role is of interest, please apply now!#LI-JM3

Contamination Control Engineer - Belgium, Geel - 6 Month ContractAre you local to Geel, and looking for your next contract role? We are recruiting for a Contamination Control Engineer, on behalf of our client, an innovative global biopharmaceutical company, supporting their mission to transform medicine and provide life-changing treatment. With an exciting new project in the pipeline, the successful candidate will be involved from design to handover and a contract extension is likely. The role is remote based, with occasional visits to their state-of-the-art facility required.If you would like to help contribute towards solutions across various fields including human vaccines, rare diseases, oncology, and many more, this Contamination Control Engineer opportunity might the next role for you!What you’ll do: Ensures microbial control of process, cleanroom and clean utility systems by setting up monitoring plans, setting limits, perform trend evaluations, define improvement actions.Perform trend evaluation and reporting of microbial data for process, cleanroom and clean utilities. Perform investigations as coordinator and/or investigation leader for deviations related to process, clean utility or cleanrooms.Provide microbial information as part of deviation to further assess the impact on product. What you’ll need: Master’s degree or equivalent in Pharmaceutical/ Biotech/ Life sciences.Extensive experience in the pharmaceutical industry of manufacturing and/or quality operations. If this role is of interest to you, please apply now! #LI-CH2

Procurement Specialist - US, North Carolina - 12 Month ContractOur client, a global pharmaceutical manufacturing organization are looking for a talented Procurement Specialist 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: Provide collaboration and input to subcontracting strategies to include bid lists, pre-qualification, compensation, award basis, risk management and other information to support commercial recommendations.Review and approval of subcontract award recommendations, change order requests, and other commercial actions to ensure compliance inclusive of negotiating and validating pricing and ensuring adherence of prime contract flow down terms and conditions.Review and monitor commercial action item requests and ensure timely processing.Collaborate with respective Building Project Managers (PMs) and Responsible Engineers/Work Package Owners (WPOs) to ensure the proposed scope and schedule are acceptable. What you'll need: Advanced knowledge of MS Excel, Word, PowerPoint, Adobe AcrobatPrevious experience in large-scale construction project work environmentsKnowledge of market researchBS in Logistics, Supply Chain Management, Business Administration or relevant field If you are interested, please apply now for immediate consideration and further information.#LI-KC2

HR Business Partner - UK, Maidenhead - 12 Month ContractOur client is a global biopharmaceutical company manufacturing plasma-derived, and recombination therapeutic products, who in turn deliver high-quality medicines that treat people with rare and serious diseases, and we are now searching on an exclusive basis with the client to appoint a HR Business Partner to join their busy and rewarding team on a contractual basis for a period of 12 months.What you'll do: Managing the changes in the UK with growth in Maidenhead and all BusinessTransformations supporting Regional Agile Lead in Project ManagementLeads all employee relations matters, including providing advice and counsel to managers concerning employee performance, policy adherence, harassment, compliance violations, grievances, conflicts, and union/works council mattersManages escalations received from the HR Operations Centres and special projects as assignedAssists in the execution of the derived strategy formed by HRBP(s) for the assigned client group What you'll need: Bachelor’s degree or equivalent in human resource management, organisational psychology, business, or related field requiredExtensive experience as a HR Generalist or Employee Relations Manager, or equivalent relevant experience working in a dynamic global organisationKnowledge of HR processes gained in a dynamic organisationExperience in a global company in a matrixed reporting environment preferred If this role is of interest, please apply now!#LI-JD1

Manufacturing/Validation Specialist - Netherlands, Arnhem - 6 Months Initial ContractHow would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!Our client is currently seeking the skills of a Manufacturing/Validation Specialist to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll need: Reviewing and approving validation tests in TLS (Tulip Validation)Drafting implementation protocols, executing change controls, and updating work processes for shopfloor implementationHands-on mentality, proactive approach, and flexible attitude to implement the EBR process as quickly as possibleAssessing implementation and validation against current GxP guidelines Desirable Experience: Change controls – Independently executingChange ControlsDocumentation updateKnowledge of current GxP regulationsFlexibility and a hands-on mindsetStakeholder / Vendor Management If this role is of interest to you, please apply now! #LI-SC1

QMS Specialist - Ireland, Cork - 12 Month ContractAre you based in Cork, looking for your next long-term contract? We are recruiting for a superb opportunity on behalf of our client, an international contract development and manufacturing organisation who help bring new and off-patent drugs to market. With a track record of over 60 years delivering advanced technologies, this organisation flies in the face of difficulty, giving their customers a service and product that cannot be found elsewhere.This role is based in Cork and is advertised on a contractual basis of 12 months.What you'll do: Responsible for ensuring that the quality systems in used are in compliance with cGMP and the associated regulatory requirementsAct as site lead for nominated quality systems (e.g. EDMS, Deviations, CAPA, Quality Management etc), responsible for trending review and resolution of issuesEnsure that quality issues are identified, addressed and resolved in a timely mannerProvide detailed knowledge of quality systems in place and ensure that root cause is identified and corrective actions as appropriate are completed What you'll need: Motivated to be an inspiring member of a high performing team.Excellent interpersonal skills: communication, decision making, people influencing skills.Ability to interact with multiple stakeholders.Excellent knowledge of relevant Quality and Compliance Guidelines (cGMP, Auditing, Quality Management Systems, Quality Agreements,Regulatory Affairs, Training) and respective regulations. If this role is of interest, please apply now!#LI-SC1