Regulatory Affairs Intern (Ha Noi)

Thỏa thuận
Thực tập
Hạn nộp hồ sơ: 29/12/2026 (Còn 54 ngày)
Ứng tuyển sớm để được ưu tiên
Kết nối với Nhà tuyển dụng để tìm hiểu thông tin và gia tăng cơ hội trúng tuyển
OMess
Nhà tuyển dụng đang online
Job Description Summary The intern will provide hands-on support across regulatory tracking, artwork confirmation, and preparation of lower-complexity post-approval change dossiers. This role offers an excellent opportunity to gain practical exposure to pharmaceutical regulatory affairs while contributing to the accuracy and efficiency of regulatory operations.Job Description
Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!
We are looking for a detail-oriented and motivated Regulatory Affairs Intern to join our Drug Regulatory Affairs (DRA) team in Vietnam.
The intern will provide hands-on support across regulatory tracking, artwork confirmation, and preparation of lower-complexity post-approval change dossiers. This role offers an excellent opportunity to gain practical exposure to pharmaceutical regulatory affairs while contributing to the accuracy and efficiency of regulatory operations.
Key Responsibilities
Support the DRA team in maintaining timely and accurate tracking of regulatory activities and dossier status across relevant systems and tools.
Perform routine data updates and maintenance to ensure regulatory information is complete and up to date.
Support artwork (AW) review and re-confirmation activities, including documentation and status tracking.
Assist with the preparation and coordination of lower-complexity post-approval change dossiers under the guidance of the DRA team.
Support the organization and maintenance of regulatory documentation.
Help identify opportunities to simplify and enhance local regulatory tracking processes.
Follow up on assigned activities to support timely completion of regulatory deliverables.
Provide other operational and administrative support to the DRA team as required.
Minimum Requirements
Final-year student pursuing a Bachelor's degree in Pharmacy or another relevant discipline.
Minimum GPA of 3.0/4.0 or equivalent.
Able to commit to a full-time internship for 6 months.
Strong attention to detail and ability to work accurately with a high volume of information and documentation.
Good organizational and time-management skills.
Good knowledge of Microsoft Excel and Microsoft Office applications; experience with data tracking or reporting tools would be an advantage.
Good communication and collaboration skills.
Good command of English and Vietnamese.
Interest in pharmaceutical regulatory affairs and willingness to learn about regulatory processes and requirements.
What You Will Learn
Practical exposure to Drug Regulatory Affairs in the pharmaceutical industry.
Understanding of regulatory dossier tracking, artwork management, and post-approval change activities.
Experience working with regulatory documentation and tracking systems.
Opportunities to develop skills in data accuracy, process improvement, regulatory compliance, and cross-functional collaboration.
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
#Sandoz
Skills Desired

Thông tin chung

  • Thu nhập: Thỏa thuận

Sandoz

Xem trang công ty
Địa chỉ công ty: Centec Tower, Unit 1601A, 72-74 Nguyen Thi Minh Khai Str, Dist 3, HCMC
Quy mô: Từ 101 - 500 nhân viên
Thông tin công việc
Vị trí:
Nhân viên
Hình thức làm việc:
Thực tập
Việc làm tương tự
Director, Market Access
Công Ty Dược Phẩm Đa Quốc Gia AstraZeneca
Hồ Chí Minh
Công Ty Dược Phẩm Đa Quốc Gia AstraZeneca
Thỏa thuận
Industry Technology Specialist (Coffee)- SEA
Novozymes Malaysia
Novozymes Malaysia
Thỏa thuận
Logistic Executive - Import-Export
CÔNG TY CP ĐẦU TƯ VÀ THƯƠNG MẠI ADM VIỆT NAM
CÔNG TY CP ĐẦU TƯ VÀ THƯƠNG MẠI ADM VIỆT NAM
Thỏa thuận
Associate Regulatory Affairs Manager, Abbott Healthcare Vietnam
Abbott Laboratories. GmbH
Bình Dương
Abbott Laboratories. GmbH
Thương lượng
Executive - Regulatory Affairs
B. Braun Group
B. Braun Group
Thỏa thuận
Cảnh báo dấu hiệu lừa đảo tuyển dụng
Thu phí và cung cấp thông tin
  • Phí hồ sơ, đồng phục, đặt cọc.
  • Yêu cầu nộp bản gốc giấy tờ.
  • Cung cấp mã OTP.
Hứa hẹn trúng tuyển 100%
  • Không yêu cầu trình độ.
  • Không cần thử việc.
Phỏng vấn bất thường
  • Địa điểm xa văn phòng công ty.
  • Phỏng vấn qua Telegram.
Yêu cầu làm nhiệm vụ
  • Tải app, nạp tiền.
  • Làm nhiệm vụ nhận thưởng.
Tin tuyển dụng sơ sài
  • Mô tả công việc chung chung
  • Nhiệm vụ đơn giản, thu nhập khủng
  • Lỗi chính tả, đánh máy.
Đội ngũ hỗ trợ của JobOKO sẵn sàng đồng hành, tư vấn và giới thiệu những cơ hội việc làm phù hợp, giúp Ứng viên tự tin phát triển sự nghiệp và chinh phục mục tiêu nghề nghiệp bền vững.
Đội ngũ hỗ trợ của JobOKO luôn chủ động tư vấn các giải pháp tuyển dụng tối ưu, cam kết đồng hành và hỗ trợ Quý Nhà tuyển dụng đạt được hiệu quả tuyển dụng bền vững.