Stefanini Group is looking for a Project Manager – Pharmaceutical in Irvine, CA that can start ASAP. The Project Manager, manages multiple cross-functional projects of medium to high complexity and supports planning of cross functional quality activities and evaluations. You will:Partner with cross functional team, manage Quality related meetings, escalations and drive decision making to ensure projects are on time and on budget.Coordinate creation/update of Quality related documentsProvide Project management of resource planning, generating metrics/ KPIs and presentation materials for management reviews and governance meetingsEnhance process alignment and drive strategic discussions within site management and among all departments at the site teams including Quality, Operation and etc.Build project plans and team assignments using Gantt charts (MS Project), estimating project costs and adhering to budget.Direct and monitor work efforts, identifying resource needs, performing business quality reviews, and escalating functional, quality, timeline and cost issues appropriately.Utilize project management processes, software and methodologies to ensure projects are delivered on time, within budget, adhere to high quality standards and meet stakeholder/customer expectations.Coordinate communication within all areas of the enterprise that impact scope, budget, risk and resources of the work being managedLead continuous improvement projects that deliver measurable gain in quality, efficiency and alignment within the site. Apply your knowledge, skills, and tools of project management / operational excellence (OPEX) to ensure optimal execution of projects, identity potential savings and continuous improvement initiatives of existing and new processes.
Requirements:Bachelor s degree in Business-related discipline required, MBA or business operations degree preferred4 years of Project Management experience, including 2 years leading medium to complex projects, and knowledge and expertise in the use of project management methodologies and tools, resource management practices and change management techniques requiredUnderstanding of Global Pharmaceutical industry landscape and business principles, GMP environment work experience and thorough understanding of biological/chemistry technology transfer processes and timelines required. Experience in small molecule and or biologics tech transfers strongly preferredAdvanced analytical skills/experience using MS Excel and other related software programsSix Sigma / LEAN Green Belt or Black Belt certification preferred1+ year of experience in Lean Manufacturing or Operational Excellence requiredDemonstrated ability to think strategically, work, and lead effectively in fast-paced, dynamic collaborative / team environmentExcellent interpersonal and verbal communication skills, writing skills, and negotiation skillsBackground and experience in Quality area.
– provided by Dice
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