Tech Transfer Manager
- Ireland, Dublin
- Contract
- Compliance / Quality Assurance
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
- 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.
#LI-TE1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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