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Tech Transfer Manager

  1. Ireland, Dublin
Dublin
  1. Contract
Competitive
  1. Compliance / Quality Assurance
37005
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Tech Transfer Manager - Ireland, Dublin - 12 Month Contract 

Are you looking for the chance to join a life changing pharmaceutical organisation in their mission to continuously drive innovation? We are recruiting for a Tech Transfer Manager to support the Dublin function. 

Essential duties and responsibilities for this role include, but are not limited to, the following:
  • Plan and execute multi-discipline Tech Transfer projects
  • Prepare project charters including business justification for new projects.
  • Responsible for the generation of project cost estimates, budgets, forecasting, and long-range plan.
  • Track project deliverables, provide regular project reporting on status to plan and KPIs, schedule and budget reports
  • Manage the decision log and risk register for the project
  • Lead the project team through all project phases from design through to regulatory submission. Engage site functional SME support (Tech Services, Operations, Engineering, and Quality etc.) as required.
  • Develop project controls (Project Execution Plan (PEP), schedule, risks) to ensure alignment of project timelines with business needs.
  • Communicate progress against plan on a regular basis and develop mitigations for project risks / delays. Prepare monthly metrics on project performance, achievements, and statistics.
  • Responsible for the project management support for the NPI/Technology Transfer of a product across the network using the TT Business Process
Desirable experience:
  • Demonstrated leadership of technical and / or operational teams or projects within a biopharmaceutical manufacturing organisation.
  • Experience within new product introduction project work is preferred.
  • Strong track record of leading in a global and matrix environment and working cross functionally with internal and external stakeholders
  • Ability to quickly establish strong, effective and enduring partnerships with internal and external stakeholders
  • Strong organisational, change management, problem solving and leadership skills
  • Strong presentation and communication skills
  • Team player with the ability to manage multiple tasks simultaneously
  • Experience of biopharmaceutical Bulk Drug Substance (BDS) manufacturing, Aseptic Fill Finish and Finished Packaging.
  • A working knowledge of regulatory requirements for pharmaceutical industry is required.
  • Operational excellence knowledge and application using Lean or six-sigma tools would be advantageous.
If this role is of interest, please apply now.
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