Project Manager (Regulatory)

Location
Islandwide
Job Type
Full-time
Experience
Mid
Category
General
Salary
$5,000 - $7,000
Posted
3 weeks ago
Expires
Jul 10, 2026
Views
4

Job Details

Vacancies

1 position

Experience Required

No experience required

Job Description

About the role

We are looking for an experienced Regulatory Project Manager to independently manage global submissions, lead cross-functional teams, and support regional regulatory strategies. This role bridges global regulatory direction with local market execution and compliance.

Key responsibilities

  • Independently manages submissions and supports major global regulatory filings.
  • Leads cross-functional team meetings alongside regulatory leads.
  • Develops, maintains, and tracks submission timelines; identifies critical paths and risks.
  • Plans and facilitates kick-off and ongoing project meetings including agenda, coordination, and presentations.
  • Documents meeting minutes, decisions, risks, and action items.
  • Maintains project plans, dashboards, and collaborative workspaces.
  • Supports regulatory activities related to contract manufacturing and product transitions, including partner coordination and compliance oversight.
  • Leads scenario planning and risk mitigation activities.
  • Tracks content plans with functional teams to ensure timely delivery.
  • Manages rapid response processes for health authority queries.
  • Supports advisory committee and health authority meeting preparations.
  • Coordinates authoring, review, and approval of regulatory documents.
  • Leads lessons-learned activities and maintains associated logs.
  • Acts as subject matter expert for local and regional regulatory requirements.
  • Supports localization of regulatory strategies and submissions per regional authority requirements.
  • Ensures compliance with country-specific regulations, formats, and timelines.
  • Provides translation support or review of submission documents in the local language, as needed.

Skills & qualifications

  • Bachelor's or Master's in Pharma, Medical, or a related scientific discipline
  • 8–10 years overall experience, with at least 2 years in project management; regulatory project management experience is a plus.
  • Strong knowledge of regional regulatory frameworks, submission processes, and compliance requirements.
  • Ability to bridge global regulatory strategies with local execution needs.
  • Experience with project management tools (e.g., MS Project or equivalent).
  • Strong conceptual and analytical thinking skills.
  • Excellent interpersonal and business collaboration skills.
  • Intermediate proficiency in MS Office (Word, Excel, Outlook).
  • Ability to multitask and prioritize in a fast-paced environment.
  • Fluency in local language (written and verbal) plus English proficiency.

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PE PHARMA PTE. LTD.

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