Executive (G12a)

**Title**:Executive (G12A)**:

- Date: Oct 30, 2023- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd- List of Responsibilities / Job Functions:
- To verify whether code creation request is initiated in compliance of Global SOP / Site SOP.
- To evaluate the new code creation scenario against the Rule book referred in Global SOP / Site SOP.
- To approve / reject the new code creation request in MDO Tool (Master data Online Tool).
- To initiate "Exception approver" workflow in MDO Tool as and when required (Specifically new code required with similar name as per existed code or duplicate code creation).
- To evaluate the global field change request (including to access impact on all user sites).
- To approve / reject global field change request in MDO Tool (Master data Online Tool).
- To ensure the compliance for new code creation process as per Global SOP / Site SOP with respect to "Global Approver" role.
- Any specific work needs to be performed by "global approver" role in MDO Tool workflow configuration.
- Any specific work allotted by the reporting authority.
- List of Competencies Required:

- Technical Competencies:
- B.Sc. / M.Sc. / B.Pharm.
- More than 5 years of experience in GMP environment.
- Knowledge of IT/computer systems.

Behavioral Competencies / Soft Skills:
- Drive results and excellence
- Customer centricity
- Good Written and verbal communication