Title: Regulatory Technical Specialist 2
Duration: 6+ months with possible extension
Prepares technical documentation for in-vitro diagnostic products to support global registrations. Communicates with regional units to ensure understanding of registration requirements. Works with different organizations to assemble technical documentation required. Updates information of submission tracking for registration projects. Uses computer system such as Teamspace, SAP, Documentum and others to retrieve and upload documentation.
Three years or more experience in regulatory affairs around In-Vitro Diagnostics. Knowledge of In-Vitro Diagnostic Directives (EU) and international registrations are highly desirable.
Please send me your confirmation that no one else has contacted you for this position apart from APN Team.
APN Software Services, Inc.
39899 Balentine Drive, Suite 385, Newark, CA 94560