Teva Pharmaceuticals is hiring for Regulatory Information Management System(RIMS) who can fulfill the following criteria.
Job location: Navi Mumbai Seawoods
Years of experience required: 2-4
If your profile matches the above requirement, please share your updated resume to email@example.com with subject line as “RIMS Associate
Roles & Responsibilities:
– Responsible for executing GRO RIM operations in line with Work Instructions and SOPs. Primarily will be RIM Central Data Service related product registration data management (includes the procurement of data from source regulatory documentation which requires a thorough understanding of the structure and contents of a regulatory dossier, and a thorough understanding of the data structures applicable to registration data and the related system workflows).
– Perform Quality Control (QC) and data integrity checking, as part of the RIM Central Data Services operation, to confirm the accuracy and completeness of the Teva Global Registration database.
– Represent GRO RIM across the wider Global Regulatory Affairs community. Must be proficient at building effective working relationships with all stakeholder and customer groups.
If your profile matches the requirement, please share your updated resume to firstname.lastname@example.org with subject line as “RIMS Associate”