Associate, Regulatory Affairs

Zuellig Pharma; Cebu City; On-site; PHP 180,000 - 420,000; Full time

Benefits offered by this job

Inclusive environment

Diversity, equity, and inclusion

Regional healthcare knowledge

Flexible work-life balance

Total Rewards program

Job summary

Zuellig Pharma Philippines is seeking an Associate, Regulatory Affairs to support the regulatory team with material maintenance, data validation, and reporting. The role emphasizes accuracy, compliance, and collaboration across teams in a fast-paced healthcare environment.

The successful candidate will perform system checks, assist with IMS/IQVIA tagging review, standardize material descriptions, and provide updates to the Regulatory Team while growing professional knowledge in regulatory

Responsibilities

• Review the IMS/IQVIA tagging of the materials.
• Review and align the material description to 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.

Job description

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Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.

Associate, Regulatory Affairs

Requisition ID: 2371

Posting Start Date: 28 Sept 2026

Location: Sun Valley, Philippines

ZUELLIG PHARMA is a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world-class distribution, digital, and commercial services to support the growing healthcare needs in this region. The company was started a hundred years ago and has grown to become a multibillion-dollar business covering 17 markets with over 12,000 employees. Our people serve more than 200,000 medical facilities and work with over 450 clients, including the top 20 pharmaceutical companies in the world.

1. Review the IMS/IQVIA tagging of the materials maintained in the system.

2. Review and align the material description as per standard format .

3. Updates and encodes the Material Maintenance Clean-up monitoring file.

4. Provides assistance on report consolidation on the activities related to Material Maintenance Clean-up.

5. Performs validation of the Material maintained in the system.

6. Performs validation of the Material maintained in the system.

7. Provide updates and reports to the Regulatory Team.

8. Performs other tasks assigned by the Regulatory Team.

WHY JOIN ZUELLIG PHARMA

• We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success.
• We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly.
• As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region.
• Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities.
• Our Total Rewards program is designed to support your overall well-being in every aspect.

Data Privacy Notice: I understand that while processing my application, my personal data may be shared internally to individuals who will be involved in assessing my application. By proceeding with my application, I hereby give my consent to Zuellig Pharma Corporation/Metro Drug, Inc. to share my personal data internally.

Zuellig Pharma promotes an inclusive, fair workplace by ensuring equitable employment and compensation based on merit, regardless of background.