• Job Description
• Qualifications for Regulatory Affairs Associate I – 1434

Teva Pharmaceuticals Regulatory Affairs Associate I Job Vacancies for B Pharmacy /M Pharmacy / Master of Life Sciences – M Pharm preferred

Job Description;

Regulatory Affairs Associate I – 1434

Location: Navi Mumbai, India, 400706

Company: Teva Pharmaceuticals

Job Id: 46383

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 stakeholders and customer groups.

Qualifications for Regulatory Affairs Associate I – 1434

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

Preferred: MS in scientific or information technology discipline.

Work Experience: Required: 1-3 years

Function; Regulatory Affairs

Sub Function; Medical Regulatory Affairs

Reports To; In the process of validation