The Senior Project Manager, Quality Projects will be responsible for managing multiple cross functional GCP and GMP submission and inspection readiness workstreams. This will include organizing teams, managing project schedules, developing project metrics, and developing material that will be presented in governance meetings. This role will collaborate with Sr. leadership within the Quality organization, as well as operational stakeholders in the GMP and GCP areas.
6+ Years | Project management experience within a biotechnology, pharmaceutical, or other relevant industry.
Minimum Bachelors' Degree in relevant discipline.
Ability to organize cross-functional teams and motivate them towards achieving common goals.
Preferable to have experiences in cell & gene therapy.
Knowledge of GxPs in a bio/pharmaceutical context.
Please apply with your most up-to-date resume and we can talk more about the role/application process.