Planner jobs in Philippines

Explore 3 matching jobs.

MSD

Regional Submission Planner

MSD

Posted: 10/21/2026
Assembly
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SupportNinja

Workforce Capacity Planner

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Posted: 9/15/2026
MSD

Regional Submission Planner

MSD
Posted 10/21/2026full-timeMakati • PhilippinesJuniorMid-LevelWebsite
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Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in regulatory submission planning and project management within the pharmaceutical industry, with a strong focus on compliance and efficiency in regulatory operations. Proficient in managing dynamic timelines and collaborating effectively in multicultural environments.

Highest-signal resume keywords
Regulatory Submission PlanningProject ManagementKnowledge of eCTDPharmaceutical Regulatory AffairsStrong Communication Skills

Tech Stack

Tools & technologies
Assembly

About the role

Key responsibilities & impact
  • Support regional planning activities for the AP region and cross-regional planning activities as needed
  • Create regulatory submission plans and track registration of regulatory submission targets
  • Plan and manage regulatory operations projects from authorization through delivery to country regulatory affairs teams and/or Health Authorities
  • Develop and maintain regulatory submission plans and project milestones
  • Facilitate and participate in cross-functional forums and meetings
  • Coordinate with the central planner based in the US headquarters
  • Drive submission assembly, publishing, delivery, and archival processes
  • Access and maintain regulatory systems and databases
  • Identify opportunities to improve submission-process efficiency
  • Participate in process improvement projects
  • Maintain knowledge of regional regulatory procedures, guidelines, and standards

Requirements

What you’ll need
  • Bachelor’s degree in a Life Science, Pharmacy or Engineering related discipline
  • At least 2 years’ experience in the pharmaceutical industry in operational roles, project management or regulatory affairs
  • Strong written and oral communication skills in English
  • Ability to multitask with proven project management capabilities
  • Ability to manage dynamic timelines, interact and negotiate with others, collaborate, and follow up effectively
  • Working knowledge of regulatory guidelines and procedures within the AP region
  • Excellent communication skills for managing interactions in a multicultural environment
  • Capability to plan, manage, track, assemble, and deliver regulatory content
  • Ability to handle time pressure and evolving priorities
  • Affinity for working with complex IT systems
  • Knowledge of electronic Common Technical Document (eCTD)
  • Knowledge of pharmaceutical regulatory affairs, pharmacovigilance, regulatory compliance, publishing, and project management

Benefits

Comp & perks
  • Hybrid work arrangement
  • Regular employee status

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Regulatory OperationsProject ManagementSubmission AssemblyRegulatory CompliancePharmacovigilanceProcess ImprovementRegulatory Guidelines KnowledgeMultitaskingTracking and Delivery of Regulatory ContentManaging Dynamic Timelines
Soft Skills
Strong Written CommunicationStrong Oral CommunicationCollaborationNegotiationAbility to Handle Time Pressure
Tools & Technologies
Regulatory SystemsDatabasesElectronic Common Technical Document (eCTD)
Industry Keywords
Pharmaceutical IndustryRegulatory AffairsAP RegionLife SciencePharmacyEngineering