Regulatory Affairs Specialist - Material & Compliance

Zuellig Pharma; Parañaque; On-site; PHP 240,000 - 420,000; Full time

Job summary

Zuellig Pharma in Metro Manila is seeking a Regulatory Data Associate to support material data maintenance and compliance processes across our healthcare supply chain. The role emphasizes accurate data handling and adherence to standard formats for material descriptions.

You will review IMS/IQVIA tagging, align descriptions, maintain the clean-up monitoring file, and assist with reporting to the Regulatory Team. Candidates will contribute to system validation and ongoing data integrity.

Qualifications

• Review IMS/IQVIA tagging of the materials maintained in the system.
• Review and align the material description as per standard format .
• Updates and encodes the Material Maintenance Clean-up monitoring file.
• Provides assistance on report consolidation on the activities related to Material Maintenance Clean-up.
• Performs validation of the Material maintained in the system.
• Provide updates and reports to the Regulatory Team.
• Performs other tasks assigned by the Regulatory Team.

Responsibilities

• Review the IMS/IQVIA tagging of the materials maintained in the system.
• Review and align the material description as per standard format .
• Updates and encodes the Material Maintenance Clean-up monitoring file.
• Provides assistance on report consolidation on the activities related to Material Maintenance Clean-up.
• Performs validation of the Material maintained in the system.
• Performs validation of the Material maintained in the system.
• Provide updates and reports to the Regulatory Team.
• Performs other tasks assigned by the Regulatory Team.

Skills

IMS/IQVIA tagging

Material data validation

Report consolidation

Job description

Zuellig Pharma in Metro Manila is seeking a Regulatory Data Associate to support material data maintenance and compliance processes across our healthcare supply chain. The role emphasizes accurate data handling and adherence to standard formats for material descriptions.

You will review IMS/IQVIA tagging, align descriptions, maintain the clean-up monitoring file, and assist with reporting to the Regulatory Team. Candidates will contribute to system validation and ongoing data integrity.