About the opportunity
Join PAHO in advancing strong, effective, and harmonized pharmaceutical regulatory systems across the Americas. This role drives strategic cooperation, regulatory convergence, and capacity strengthening to improve access to quality, safe, and effective health technologies. Under the general supervision of the Director, Innovation, Access to Medicines and Health Technologies (IMT) and the direct supervision of the Unit Chief, Quality and Regulation of Medicines Health Technologies (QR), the incumbent provides strategic leadership for regional technical cooperation, leads technical guidance on the implementation of the WHO Global Benchmarking Tool, serves as Technical Secretariat of PANDRH, and promotes alignment between regulatory strengthening activities and regional programs.
Salary and benefits
- Annual salary of Step I – 86,027.00 USD
- Post adjustment – annually of 46,970.74 USD
Who can apply?
- A university degree in pharmacy or related discipline and a master’s degree in regulatory affairs, public health or other health science related to the functions of the position from a recognized institution.
- Nine years of combined national and international experience in the implementation and administration of programs and projects related to the regulation of pharmaceuticals.
- Fluency in Spanish or English with a working knowledge of the other language.
Required documents
- On-line profile
- Scanned copy of official degree(s)/diploma(s)/certificate(s) required for this position (if retained for an interview)
When to apply
- Job Posting: August 11, 2026
- Closing Date: September 2, 2026, 11:59 PM Eastern Time
How to apply
- Complete an on-line profile to be considered for this post.
Additional information
- Contractual Agreement: Staff – Professional Post
- Grade: P-4
- Duration of Contract: One year. Post of limited duration. First year probationary period.
Our Take on This Opportunity
This section reflects Open Opportunities’ own analysis of the opportunity from an applicant’s perspective.
You may be a strong fit if…
- Professional with a degree in pharmacy and a master's in regulatory affairs or public health.
- Nine years of experience in the administration and implementation of pharmaceutical regulatory programs.
- Expertise in the WHO Global Benchmarking Tool and regional regulatory harmonization.
What should you think carefully about?
- This is a one-year, limited-duration professional staff post.
- The role is based on-site in Washington, D.C., requiring relocation if you are not local.
- Fluency in English or Spanish is required, with a working knowledge of the other.
How could this fit your current goals and plans?
This position is perfect for a regulatory expert looking to drive strategic change in pharmaceutical access and safety across the Americas. It provides a high-level platform to lead regional technical cooperation and influence regulatory standards at the WHO level.
Our take
Regulatory affairs professionals with deep experience in pharmaceutical systems should apply. It is less suitable for those seeking permanent staff roles or remote work arrangements.
Ready to apply?
Review the opportunity on the official website before applying.
Official-source verified
