Vacancy expired!
- Collaborate with Quality Leadership to develop and scope submission and inspection readiness workstreams. This will include identifying project team members for given workstreams
- Create and manage workstream project schedules according to business needs.
- Ensure deliverables are monitored to the agreed upon timelines, collaborating with workstream leads
- Work with teams to resolve and find solutions to challenges as they come up. Will escalate project and scheduling challenges that are unable to be resolved to management
- Collaborate with teams to develop metrics to measure progress and highlight any areas of focus
- Set-up and facilitate routine meetings to drive the project and create awareness
- Create meeting materials used for project status updates at governance meetings.
- Bachelor's degree in life sciences, computer science, economics or other discipline requiring quantitative skills preferred
- 6 to 8 years of experience in biopharmaceutical/pharmaceutical or related industry with strong background in quality and continuous improvement
- Experience with organizing cross functional teams and motivating them to achieve common goals
- Preference for experience in managing regulatory submission projects
- Preference for experience in cell and gene therapy
Vacancy expired!