Mô tả công việc
Reports To:
Location:
Type: Full-time
Job Summary:
The Head of Regulatory Affairs will lead and oversee all regulatory strategies and activities to ensure the company's pharmaceutical products comply with applicable laws and regulations in domestic and international markets. This leadership role involves managing submissions, approvals, and maintaining relationships with regulatory authorities to facilitate smooth product registrations and market access.
Key Responsibilities:
Regulatory Strategy & Compliance
Develop and implement comprehensive regulatory strategies for product registration, approval, and lifecycle management in multiple markets.
Ensure compliance with local and international pharmaceutical regulations (e.g., FDA, EMA, WHO, ICH guidelines).
Monitor changes in regulatory requirements and proactively communicate their impact on the business.
Product Registration & Submissions
Oversee preparation, review, and submission of dossiers for new product registrations, renewals, variations, and post-approval changes.
Coordinate timely and successful approvals from health authorities and regulatory agencies.
Team Leadership & Management
Lead, mentor, and develop a team of regulatory affairs professionals.
Allocate resources effectively to meet project timelines and business goals.
Foster a culture of compliance, continuous learning, and professional development.
Cross-Functional Collaboration
Work closely with R&D, Quality Assurance, Manufacturing, and Marketing teams to ensure regulatory requirements are integrated into product development and commercialization.
Provide regulatory guidance and risk assessment throughout product lifecycle.
Liaison with Regulatory Authorities
Establish and maintain effective relationships with regulatory agencies and authorities.
Represent the company in meetings, inspections, and audits by regulatory bodies.
Documentation & Reporting
Ensure all regulatory documentation is accurate, complete, and up-to-date.
Prepare regulatory reports, risk assessments, and compliance statements for internal and external use.
Yêu cầu
Qualifications:
Bachelor's or Master's degree in Pharmacy, Life Sciences, Chemistry, or related field.
Minimum 8-10 years' experience in pharmaceutical regulatory affairs, including at least 3 years in a managerial or leadership role.
Deep knowledge of regulatory requirements and submission processes in key markets (e.g., Vietnam, ASEAN, US, EU).
Experience with electronic submission systems (eCTD) and regulatory databases.
Strong leadership, communication, and negotiation skills.
Ability to work under pressure and manage multiple projects simultaneously.
Key Skills:
Regulatory strategy development
Product registration & dossier management
Knowledge of international regulatory frameworks (FDA, EMA, WHO, ICH)
Team leadership and project management
Risk assessment & mitigation
Strong interpersonal and stakeholder management skills
Preferred:
• Experience in pharmaceutical product lifecycle management
• Familiarity with GMP, GDP, and other quality standards
• Ability to work independently and as part of a team
• Proficiency in English (written and spoken)
Quyền lợi
Competitive salary (negotiable based on experience) with allowance.
Dynamic, professional, and growth-oriented work environment.
Comprehensive health, social, and unemployment insurance.
Opportunity for professional development through training and workshops.
Lunch and parking allowance.
Annual performance-based reviews and salary increments.
Company trips and team-building events.
Thông tin khác
Thời gian làm việc
Thứ 2 - Thứ 6 (từ 08:00 đến 17:30)
Thông tin chung
Nơi làm việc
- - Hồ Chí Minh: 91 Nguyễn Hữu Cảnh, Phường Thạnh Mỹ Tây (quận Bình Thạnh cũ)
Cách thức ứng tuyển
Ứng viên nộp hồ sơ trực tuyến bằng cách bấm nút Ứng tuyển bên dưới:
Hạn nộp: 23/07/2026
