Scan Jul 30 Internship – APAC RIO (Regulatory) Apply · 6/10 risk Pfizer · Malaysia - Kuala Lumpur

10xCareer; Kuala Lumpur; On-site; MYR 8,900 - 18,000; Full time

Job summary

Pfizer Malaysia in Kuala Lumpur offers an internship – APAC RIO (Regulatory) to work on APAC regulatory guidelines, Veeva Vault RIM operations, and automated data extraction. The role involves producing correspondence, maintaining records, and preparing country regulatory documents with close collaboration across internal teams.

Ideal for candidates seeking exposure to multi-country regulatory filings and cross-departmental coordination in a global pharma setting.

Qualifications

• Auditing multi-country regulatory filings against strict health authority mandates.
• Navigating cross-departmental relationships and external stakeholder communication.
• Managing contextual decisions for ad-hoc operational requests.

Responsibilities

• Produce correspondence and documents.
• Maintain records and databases.
• Navigate ARIBA and GCMA systems.
• Liaise with internal staff.
• Prepare country regulatory documents.

Skills

APAC regulatory guidelines

Veeva Vault RIM operations

Automated data extraction

Job description

Worth applying Pfizer Malaysia - Kuala Lumpur

Internship – APAC RIO (Regulatory)

Skills and tasks

• APAC Regulatory Guidelines
• Veeva Vault RIM Operations
• Automated Data Extraction

Skill-to-task connections are not available yet.

Tasks from the posting

produce correspondence and documents

produce correspondence and documents

AI does it

maintain records and databases

maintain records and databases

AI does it

navigate ARIBA and GCMA systems

navigate ARIBA and GCMA systems

You + AI

liaise with internal staff

liaise with internal staff

Your edge

prepare country regulatory documents

prepare country regulatory documents

You + AI

Prepare for this role

Practice an interview or plan your next steps with AI Coach.

of this job is already automatable.
40% is classified as human or shared work.

2 AI does it 2 You + AI 1 Your edge of 5 duties

Your edge 3 things

• Auditing multi-country regulatory filings against strict health authority mandates.
• Navigating cross-departmental relationships and external stakeholder communication.
• Managing contextual decisions for ad-hoc operational requests.

The field growing 2-3 years

Expanding healthcare access and evolving pharmaceutical regulations across the APAC region drive sustained demand for regulatory management. Strict health authority oversight prevents regional drug submission oversight from being eliminated.

Do this week

• 01 APAC Regulatory Guidelines Mastery of regional health authority rules increases long-term value in pharmaceutical regulatory operations.
• 02 Veeva Vault RIM Operations Proficiency with industry-standard regulatory platforms improves mobility across global pharma companies.
• 03 Microsoft Copilot produce correspondence and documents and maintain presentations, records, spreadsheets and databases;