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Project Manager (Regulatory)

Mức lương
20 - 22 triệu
Khu vực tuyển
Kinh nghiệm
5 năm
Hạn nộp hồ sơ:
14/07/2026
Ứng tuyển sớm để được ưu tiên!

Mô tả công việc

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.

 

Yêu cầu công việc

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.

Quyền lợi

  • Flexible work arrangements (full-time, part-time, or project-based; remote or on-site)
  • Competitive salary 
  • Professional growth and skill development 
  • Exposure to international projects and diverse product categories
  • Opportunity to manage projects independently and contribute to process improvements

Thông tin chung

Ngày đăng
15/06/2026
Cấp bậc
Chuyên gia
Số lượng tuyển
1
Hình thức làm việc
Theo hợp đồng tư vấn
Yêu cầu kinh nghiệm
5 năm
Ngành nghề

Kỹ năng cần thiết

Phân tích dữ liệu
Pháp chế Dược phẩm
Microsoft Office
Giao tiếp
Quản lý dự án

Địa điểm làm việc

Hà Nội:Tang 8, Toa nha Licogi 13, so 164 Khuat Duy Tien, Thanh Xuân
Văn phòng đại diện PE PHARMA PTE.LTD. tại thành phố Hà Nội
Văn phòng đại diện PE PHARMA PTE.LTD. tại thành phố Hà Nội
Địa chỉ:1 Commonwealth Lane, #07-12, One Commonwealth, Singapore 149544. được thành lập Văn phòng đại diện tại thành phố Hà Nội Điều 2. Tên Văn phòng đại diện
Quy mô:Chưa cập nhật
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