Regulatory Affairs Intern (Ha Noi)
About this opportunity
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 at least 3 working days per week 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
Job details
How this role compares
Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.
We currently track 29 comparable Intern/Fellow/Postdoc Regulatory Affairs roles across 19 biopharma companies.
Salary context
1 of 29 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 29 comparable roles
+ 8 more countries
Seniority mix
29 of 29 peers have a known seniority level
Therapeutic area mix
2 of 29 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.