AP Regional Submissions Planner — Cross-Region Delivery

MSD; Makati; Hybrid; PHP 900,000 - 1,300,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

MSD is seeking a Specialist Regional Submissions Planner in the Philippines (Makati) to support the AP region’s regulatory submission planning and tracking. You will work with GRACS and RRO teams to ensure timely, high-quality regulatory and safety submissions across product lifecycles.

Responsibilities include developing submission plans, coordinating cross-functional forums, and collaborating with regional and HQ planners.

Qualifications

• Bachelor’s degree or higher in Life Science, Pharmacy or Engineering.
• 2+ years in pharma operations, regulatory affairs or project management.
• Strong written and oral English communications.

Responsibilities

• Plan and manage regulatory operation projects from authorization through delivery to country/regional teams.
• Develop and maintain the regulatory submission plan and milestones.
• Coordinate cross-functional forums to ensure timely execution of submissions.
• Collaborate with the HQ planner on assigned products/projects.
• Facilitate submission assembly and archiving with publishing teams.
• Maintain regulatory systems and databases for daily operations.
• Identify process improvements to increase submission efficiency.

Skills

Project management

Communication

English proficiency

Education

Bachelor’s degree in Life Science/Pharmacy/Engineering

Job description

MSD is seeking a Specialist Regional Submissions Planner in the Philippines (Makati) to support the AP region’s regulatory submission planning and tracking. You will work with GRACS and RRO teams to ensure timely, high-quality regulatory and safety submissions across product lifecycles.

Responsibilities include developing submission plans, coordinating cross-functional forums, and collaborating with regional and HQ planners.