Project Manager (Regulatory)
Hạn nộp hồ sơ:
14/07/2026
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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
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Microsoft Office
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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
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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