Senior Regulatory Affairs Executive - Pharmaceuticals Division
Hạn nộp hồ sơ: 25/10/2026 (Còn 59 ngày)
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JOB DESCRIPTION:
ABOUT ABBOTT
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
WORKING AT ABBOTT
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
Career development with an international company where you can grow the career you dream of.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
In Vietnam, Abbott's Established Pharmaceuticals Division has committed to enhance the care of patients. Our products cover several therapeutic areas, including gastroenterology, women health, cardiology, primary care, specialty and food supplement. Our key prescription products include Lipanthyl, Klacid, Duphaston, Drosperin and BetaSerc. Our key over-the-counter products are Duphalac, CG210, Estraceptin, Brufen, Fatig, Surbex. We also have the Influvac vaccine.
MAIN PURPOSE OF ROLE
Experienced professional individual contributor that works under limited supervision.
Apply subject matter knowledge in the area of Regulatory Affairs.
Require capacity to apply skills/knowledge within the context of specific needs or requirements.
Handle process of registration of new products, maintenance of all approved products in Vietnam and operate marketed products according to local regulations.
MAIN RESPONSIBILITIES
Registration of New and Existing Products
Reviews and compiles registration dossier for prompt renewal/initial/ variation registration
Ensures availability of updated registration documents/samples
Fast requisition of dossier and check requests
Initiates/monitors/updates Regulatory Report in timely manner
Registration of Promotion Materials
Register and compiles registration dossier for promotional material
Ensures all promotional materials are lawfully compliance
Regulatory Intelligence
Be aware of coming new regulation/change that impact to regulatory or business
Inform head of Department/contacts all change and upcoming new regulations
Implement new regulation properly
Regulatory Compliance
Ensures that all exempt regulated products are MOH verified prior to production use
Ensures that all product labels/package inserts are updated as approved by MOH's regulation.
Keeps registration record updated at all times and promptly submits books and records as per schedule
Cross-function Support
Ensures prompt coordination with other departments/units such as Sales & Marketing on regulatory and corporate matters
Ensures correctness of received documents vs information submitted
Administrative
Ensures that all technical documents/dossiers and registration samples are kept in secured place
Maintains proper filing of protocol and other regulatory and clinical related documents
Keeps updated files of MOH Regulations
BACKGROUND/ EXPERIENCE REQUIRED
Bachelor of Pharmacy
Strong knowledge of Vietnamese pharmaceutical regulations.
Minimum 3 years of experience in Regulatory Affairs, preferably with a local pharmaceutical company.
Experience in R&D or QA or QC will be an added advantage.
Language skills: Vietnamese, English
Computer skills: MS Office The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Regulatory Operations
DIVISION:
EPD Established Pharma
LOCATION:
Vietnam > Thuan An : Binh Duong Plant 1
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
ABOUT ABBOTT
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
WORKING AT ABBOTT
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
Career development with an international company where you can grow the career you dream of.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
In Vietnam, Abbott's Established Pharmaceuticals Division has committed to enhance the care of patients. Our products cover several therapeutic areas, including gastroenterology, women health, cardiology, primary care, specialty and food supplement. Our key prescription products include Lipanthyl, Klacid, Duphaston, Drosperin and BetaSerc. Our key over-the-counter products are Duphalac, CG210, Estraceptin, Brufen, Fatig, Surbex. We also have the Influvac vaccine.
MAIN PURPOSE OF ROLE
Experienced professional individual contributor that works under limited supervision.
Apply subject matter knowledge in the area of Regulatory Affairs.
Require capacity to apply skills/knowledge within the context of specific needs or requirements.
Handle process of registration of new products, maintenance of all approved products in Vietnam and operate marketed products according to local regulations.
MAIN RESPONSIBILITIES
Registration of New and Existing Products
Reviews and compiles registration dossier for prompt renewal/initial/ variation registration
Ensures availability of updated registration documents/samples
Fast requisition of dossier and check requests
Initiates/monitors/updates Regulatory Report in timely manner
Registration of Promotion Materials
Register and compiles registration dossier for promotional material
Ensures all promotional materials are lawfully compliance
Regulatory Intelligence
Be aware of coming new regulation/change that impact to regulatory or business
Inform head of Department/contacts all change and upcoming new regulations
Implement new regulation properly
Regulatory Compliance
Ensures that all exempt regulated products are MOH verified prior to production use
Ensures that all product labels/package inserts are updated as approved by MOH's regulation.
Keeps registration record updated at all times and promptly submits books and records as per schedule
Cross-function Support
Ensures prompt coordination with other departments/units such as Sales & Marketing on regulatory and corporate matters
Ensures correctness of received documents vs information submitted
Administrative
Ensures that all technical documents/dossiers and registration samples are kept in secured place
Maintains proper filing of protocol and other regulatory and clinical related documents
Keeps updated files of MOH Regulations
BACKGROUND/ EXPERIENCE REQUIRED
Bachelor of Pharmacy
Strong knowledge of Vietnamese pharmaceutical regulations.
Minimum 3 years of experience in Regulatory Affairs, preferably with a local pharmaceutical company.
Experience in R&D or QA or QC will be an added advantage.
Language skills: Vietnamese, English
Computer skills: MS Office The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Regulatory Operations
DIVISION:
EPD Established Pharma
LOCATION:
Vietnam > Thuan An : Binh Duong Plant 1
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Thông tin chung
- Thu nhập: Thỏa thuận
Việc làm tương tự khác
Công ty TNHH Thương Mại Đầu Tư Tây Hà
Bình Dương
Từ 10-20 triệu VND
Công ty TNHH Asama Yuh Jiun International Việt Nam
Bình Dương
Thỏa thuận
CÔNG TY TNHH GIẢI PHÁP CÔNG NGHỆ ECO-SMART
Hồ Chí Minh, Bình Dương
8,000,000 - 10,000,000 VND
Công ty TNHH Jang Trim
Hồ Chí Minh, Bình Dương, Đồng Nai
10 - 14 triệu VND
Abbott Laboratories. GmbH
- Địa chỉ công ty: Tầng 8, 2 Ngô Đức Kế, Bến Nghé, Quận 1, Hồ Chí Minh
- Quy mô: Từ 1000 - 5000 nhân viên
- Lĩnh vực: Y tế - Dược, Chăm sóc sức khỏe, Kinh doanh
Thông tin công việc
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Nhân viên
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