Associate Director, Project Management

职位 Associate Director, Project Management
分类 研发
汇报对象 Director of Project Management in US
工作地点 Suzhou

This position is responsible for managing the projects for both US and China filling products, ensuring that project timelines are established, communicated, and kept on track by identifying challenges, convening those required to meet them. This position needs to coordinate with various departments in China and US corporate to ensure timely completion of the project according to the plan. The incumbent will drive the completion of projects with high quality, on budget, on time meeting company EHS, cGMP, cGLP and cGCP requirements. This position also will be involved pre-formulation, development, validation, and launch projects.

  • Develop and maintain timely full-scale project plans and associated communications document to support Suzhou Projects (both China filing products and US Products).
  • Accurately communicate project status, identify potential projects problems and alert management in a timely manner.
  • Continuously review project status, independent and with the team, to ensure projects are completed on time, on budget and meet Quality, EHS, Regulatory, and GMP requirements.
  • Coordinate various departments (including employees in the US and China) to ensure timely completion of the project according to the plan.
  • Identify good practices across programs and departments, communicate the efficiencies to leadership and take initiative to improve efficiency in all functional areas to get all projects being completed in an effective way.
  • Other duties as assigned by superior such as, but not limited to project lead meetings, represent the Director of Project Management at meetings, provide routine reports for status updates.
  • BS/MS in a scientific discipline is required; ideally pharmacy, chemistry or engineering; an advanced science degree or MBA is desirable;
  • Over 10 years’ R & D project management experience or products development experience in a pharmaceutical or biotech industry.
  • Strong knowledge in generic drug development process, formulation development, analytical method development and cGMP/cGLP.
  • Strong Project Management and coordination skills; strong People Management and leadership skills; and strong communication skills.
  • A sense of urgency mixed with respect to quality.
  • Fluent (spoken & written) in both English and Mandarin.