Associate Regulatory Affairs

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

Job Description:

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.

• 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.

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.

Note: You may view the Zuellig Pharma Data Privacy Policy thru this link for reference - https://www.zuelligpharma.com/privacy-policy .

Requirements: