DESCRIPTION: This position is to support business reorganization project as the key quality contact. This position is responsible for ensuring that the project maintains compliance and documents all activities as required by applicable FDA cGMP regulations as well as procedures and standards. The employee must be able to partner internally within quality organization to drive all quality priorities with the project team. This employee must be able to self-manage and work effectively with internal parties, manufacturing sites, and corporate personnel with minimal direct oversight. Oversee Quality and GMP related aspects of the project and qualification activities.
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