Global Health Regulatory Affairs Associate

Zuellig Pharma; Parañaque; On-site; PHP 279,000 - 502,000; Full time

Job summary

Zuellig Pharma is a leading healthcare solutions company in Asia, focused on making healthcare more accessible across 17 markets with extensive distribution and regulatory support. The role involves reviewing IMS/IQVIA tagging, aligning material descriptions to standard formats, and supporting the Regulatory Team with data and reports.

The candidate will perform validation of material maintained in the system, assist in consolidating reports, and handle additional tasks as directed by the

Qualifications

• Experience with IMS/IQVIA tagging and alignment of material descriptions.
• Proficient in validating material data maintained in the system.
• Experience preparing and providing updates to the Regulatory Team.

Responsibilities

• Review IMS/IQVIA tagging of materials in the system.
• Review and align material descriptions to standard formats.
• Update and encode the Material Maintenance Clean-up monitoring file.
• Assist with report consolidation for Material Maintenance Clean-up activities.
• Validate materials maintained in the system.
• Provide updates and reports to the Regulatory Team.
• Perform other tasks assigned by the Regulatory Team.

Skills

IMS/IQVIA tagging

Material maintenance validation

Data/report consolidation

Job description

Zuellig Pharma is a leading healthcare solutions company in Asia, focused on making healthcare more accessible across 17 markets with extensive distribution and regulatory support. The role involves reviewing IMS/IQVIA tagging, aligning material descriptions to standard formats, and supporting the Regulatory Team with data and reports.

The candidate will perform validation of material maintained in the system, assist in consolidating reports, and handle additional tasks as directed by the