Company Info

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

• 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.

Qualifications

Minimum Educational Qualifications:

 

Required: Bachelor’s Degree in Life Sciences or Information Technology.

Preferred: MS in scientific or information technology discipline.

 

Function

Sub Function