
Tuyển dụng Regulatory Affairs Specialist tại Hồ Chí Minh
Việc này đang được đăng ở 2 nơi trên 2 nền tảng (VietnamWorks, TopCV)
| Nền tảng | Tiêu đề tin | Lương ghi trong tin | Hạn nộp | CV Work thấy từ |
|---|---|---|---|---|
| TopCV | Regulatory Affairs Specialist | không ghi | 20/08/2026 (đã qua) | 17/08/2026 |
| VietnamWorks | Regulatory Affairs Specialist | không ghi | 28/09/2026 | 06/08/2026 |
Các tin ghi khác nhau về hạn nộp — ô tô đậm.
Lịch sử tuyển vị trí này: CV Work ghi nhận tin đầu tiên ngày 26/07/2026, đến nay đã có 4 tin đăng trên 2 nền tảng; lần gần nhất 17/08/2026.
Mô tả công việc Regulatory Affairs Specialist
We are seeking an experienced Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for ensuring compliance with all applicable regulations and standards related to food, pharma, and personal care products, including blending, mixing, and sourcing of ingredients. The role formally reports to the General Manager of IMCD Vietnam with a dotted reporting line to the Head of HSEQR of the Asia and Pacific region. This is a critical role in our organization, and the successful candidate will have a significant impact on the quality and safety of our products and the satisfaction of our customers.
Responsibilities:
• Support the implementation and maintenance of IMCD’s Regulatory Affairs Policy and related Quality Management System.
• Coordinate implementation of ISO certification, prepare for and schedule internal- and external audits.
• Ensure all SOP’s procedure are in place.
• Ensure local legislation and governance compliance.
• Timely ensuring Corrective actions plan for Customer, external, internal audits.
• Support and coordinate Non-Conformance Reports, define and propose corrective and preventive measures.
• Participate and execute Regulatory Affairs' KPI targets
• Support for Import Compliance process, ongoing monitoring of the daily screening process and act as the go-to person in case of questions or concerns.
• Ensure HS code management, SDS management, supplier evaluation program in place.
• Ensure compliance with local legislation/regulation in respect of Regulatory Affairs matters, including ensuring that (i) all food, pharma, and personal care products comply with applicable regulations and standards, including but not limited to FDA, EU, and other global regulatory and (ii) all blending and mixing processes are conducted in compliance with regulations and standards.
• Learn and implement the company's regulatory compliance program, policies, and procedures.
• Monitor regulatory developments and changes that may affect the company's products or operations and advise management accordingly.
• Review and ensure all labelling to ensure compliance with regulations and standards.
• Support and ensure the regulatory aspect of sourcing of ingredients from traders, including ensuring compliance with applicable regulations and maintaining the required documentation.
• Collaborate with cross-functional teams, including ‘production (blending, mixing)’, sales, and marketing, to ensure that all products are in compliance with local, regional, and global regulations and standards.
• Develop and maintain positive relationships with regulatory authorities and industry associations.
• Provide regulatory guidance to internal teams.
Yêu cầu công việc
• Master’s degree in chemistry / sciences.
• Ideally 5-8 years of work experience in Regulatory Affairs roles with increasing responsibility in a reputed Industrial Chemicals business (having experience across Pharma, Food, PC consultancy role either as an expert or as an auditor.
• Solid background and proven record of accomplishment in quality management.
• Understanding of quality systems requirements and regulatory/legal framework and the development of sustainability related systems.
• Analytical and problem-solving skills with a quality mind-set.
• Effective communication and interpersonal skills at all levels.
• Ability to connect and gain commitment from all IMCD stakeholders.
• Dealing with cultural differences (e.g., colleagues, authorities, and customers).
• Experience with global quality procedures and documents.
Quyền lợi
- Thưởng:
- Attractive salary
- 13th month salary and Annual Performance Bonus - Chăm sóc sức khoẻ: Premium insurance starting after you passed probation
- Nghỉ phép có lương: 16-day paid annual leave and 4-day paid sick leave
Nhà tuyển dụng Công Ty TNHH IMCD Việt Nam
Công Ty TNHH IMCD Việt Nam · Hồ Chí Minh

Công Ty TNHH IMCD Việt Nam là nhà tuyển dụng ngành Dược phẩm / Y tế / Công nghệ sinh học, quy mô 100-499. Hiện đang tuyển 1 vị trí tại Hồ Chí Minh.
IMCD Việt Nam tuyển dụng — xem tất cả việc làm đang tuyển →
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