Specialist Regulatory Affairs
3 weeks ago
**Job Description**:
**_ (_**_ - Weight out of 100%)_
- Maintain the process for updating label based on requirement of Global for responsible products
- Assist in the monitoring of PV system if any.
- Assist for Product quality control together with SCM team if any.
**_ (_**_ - Weight out of 100%)_
- Obtain regulatory approval within optimum timelines and subsequently ensure new products are made accessible in the fastest time possible.
- Ensure immediate regulatory authority notification in relation to medicine changes.
- Help to maintain high quality and accurate packaging and labeling of MSD products.
- Develop and implement services to assist in delivering better value to customers.
- Specific measures as per personal performance grid.
**Search Firm Representatives Please Read Carefully**
**Employee Status**:
Regular
**Relocation**:
No relocation
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Number of Openings**:
1
**Requisition ID**:R203444
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