Project Initiation Lead
to support the Global Engineering Capital Projects for Lonza in Slough, UK! Relocation assistance is available for eligible candidates and their families, if needed. In this role you will be responsible to provide leadership and deliver capital investment project from Initiation through to beneficial use. You will also lead cross functional teams and will be the single point of contact for Project Initiation activities in Global Engineering team. Key responsibilities:
Ensure the project is set up to align with and deliver the Global Engineering Front end initiation process. Keep control of project costs, scope, deliverables and schedule. Address critical issues and implement appropriate mitigations for risks affecting the project delivery. Screen incoming business ideas/request, at all stages and develop an appropriate project execution strategy. Responsibility for setting project budgets, schedule baselines and appropriate project controls strategy, including management of scope changes for successful delivery of the project objectives. Supervise several Lonza and 3rd party contractor discipline leads, e.g. Project Managers of EPCMV companies will directly report to this position when Lonza works with an EPCMV contractor. Key requirements:
Master degree in Engineering (process, pharmaceutical, biochemical engineering or equivalent) or long time and in-depth project management or operational experience in multiple international environments. Leadership / management of Large Capital Projects (>200mCHF) in chemical, biochemical, pharmaceutical industries, GMP facility with experience and expertise in the field of site/facility/process and utility functionality, setup and layout, knowledge of current technology in the field of building, building technology, Drug Substance processes, automation (IT/OT/MES) technologies. Experience of Target Value Design principles and application would be an advantage. Facility design for small scale GMP clinical manufacturing, AD/PD and R&D Labs, Process Modelling, HVAC design, Personnel and Material Flows, Waste management, ATEX, design and handling of low OEL products, Clean Utilities (WFI, Purified Water, Autoclaves), Black Utilities, Process Gases storage & distribution. Expert knowledge of CDM regulations and construction management skills. Expert Knowledge of Environmental and Sustainability practices applicable to design of pharmaceutical facilities. Pharmaceutical Industry standards, Good practices and Quality requirements. Proven understanding of MHRA, FDA and EU Regulations. Excellent problem solving and Project Management skills. Good grasp of Project Control techniques and financial competence. English proficient.
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