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Teva Associate Director Project Management 
United States, Utah, Salt Lake City 
148656857

30.06.2024

The Associate Director, Project Management has overall responsibility and accountability for end-to-end planning, coordination, and execution of high priority supply projects within the site to achieve and support both local and global initiatives and goals. Key projects included are (but not limited to): New Product Launches, Site Transfers, Alternate Materials, and Continuous Improvement projects. In addition, the Sr. Manager, Project Management will manage and maintain develop the team of Project Managers for the SLC Campus.

How you’ll spend your day
  • Be responsible for all new site transfers, launches and material change projects/ planning.
  • Oversight of all site projects and determination of strategy for prioritization and resourcing
  • Work closely with MS&T, Engineering, and Transformation to determine need for project management support of significant activities.
  • Establish processes and standards for Project Management; ensure consistent implementation of these standards amongst the project management team.
  • Ensure that the project team roles and responsibilities are clearly defined, understood and that the capability exists to fulfil the responsibilities.
  • Lead cross-functional teams to successful delivery of assigned projects to time, cost, and quality in accordance with Teva strategy and priorities.
  • Develop, Manage, facilitate, and maintain all relevant project documentation and content leveraging Project Management systems and tools.
  • Enable efficiency and excellence in launch execution through to successful project completion.
  • Collaborate across different departments to drive solutions, timelines, and accountability.
  • Lead multiple groups within the site to ensure strategic initiatives are executed according to project timelines.
  • Ensure that different market requirements are implemented correctly and on time to secure successful project completion.
  • Resolve any issues that may hinder the successful completion of the project. Escalate risk to senior management, providing details such as cost, timing, and capacity to support decisions.
  • Work with the key stakeholders to prepare, maintain and coordinate the project plans based on various inputs including Project information, strategy, demand forecast, regulatory and manufacturing/packaging plans.
  • Oversee project plans while ensuring alignment with the site objectives, KPI’s and market requirements.
Your experience and qualifications

⦁ Bachelors Degree
⦁ Minimum 5 years of experience in project management of multiple complex projects preferred.
⦁ An understanding of regulatory and quality aspects for Pharmaceuticals, Food or Medical Device industries required.
⦁ Current Project Management Professional (PMP) Certification strongly preferred.
⦁ Good understanding of project management, procurement, planning and supply chain processes.
⦁ Ability to lead cross functional, matrixed project teams and gain buy-in required.
⦁ Ability to develop and maintain a good knowledge of the materials/products in specific portfolio.
⦁ Strong knowledge of GMP and RA requirements within the manufacturing and packaging environments for pharmaceuticals, Biologics, Food or Medical Device.
⦁ Strong knowledge of pharmaceutical processing, equipment, and data collection systems.
⦁ Understanding of supply chain including purchasing and negotiating processes.
⦁ Knowledge of financial functions required.


Reports To

Senior Director, Supply Chain

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