# \[e-drug\] Job Opportunity at USP

**URL:** <https://talk.edrugplus.org/t/e-drug-job-opportunity-at-usp/29462>\
**Category:** e-drug\
**Created:** [March 4, 2008, 5:28pm UTC](https://talk.edrugplus.org/t/e-drug-job-opportunity-at-usp/29462 "2008-03-04T17:28:31Z")\
**Posts on this page:** 1\
**Page:** 1

<div class="post-metadata">

**Author:** ![Jeri\_Hawthorne](https://avatars.discourse-cdn.com/v4/letter/j/5fc32e/32.png) [@Jeri\_Hawthorne](https://talk.edrugplus.org/u/Jeri_Hawthorne)\
**Post date:** [March 4, 2008, 5:28pm UTC](https://talk.edrugplus.org/t/e-drug-job-opportunity-at-usp/29462/1 "2008-03-04T17:28:31Z")

</div>

E-DRUG: Job Opportunity at USP  
-----------------------------------------------------------

Hi everyone. Below is a current opening that we have at USP in our  
International Technical Alliances Program (ITAP) department. If you are  
interested, I encourage you to take a look at our website.

Thanks,

Jeri Hawthorne  
USP  
E-mail: JRH@usp.org

External Job Description:

Function of the Position:  
This is a professional position in USP's International Technical  
Alliances Program (ITAP) Department in which the incumbent manages USP's  
participation in specific outreach programs, including contracts with  
John Snow International and Population Services International. The  
manager supports the Chief Global Services Officer (CGSO) in efforts to  
acquire new grants and contracts for drug quality initiatives in  
developing countries. He/she stays abreast of new anti-malarial and  
other drug development as well as international trends in prevention and  
treatment in this area. The Manager, USP Drug Quality Partnerships also  
takes a leadership role in maintaining USP's position as an expert  
resource in drug quality assurance and quality control for  
pharmaceuticals.  
Job Duties:  
Develop strategies, methods, and materials to ensure and support QA and  
QC within the in-country post-marketing approval supply chain for the  
DELIVER Project, Task Order 3.  
Provide technical assistance to in-country malaria programs, essential  
drugs programs that handle malaria products, and national drug  
regulatory authorities to strengthen local capacity for QA/QC including:  
assessing laboratory conformity to GMP, developing SOPs, assisting with  
ISO certification readiness, and improving the application of drug  
quality control testing methods.  
Coordinate the design and implementation of field-based drug quality  
surveillance.  
Ensure coordination of USP's work on anti-malarial drug monographs and  
reference standards.  
Support the DELIVER QA manager and the procurement manager in the  
design and implementation of a QA/QC program to ensure pharmaceutical  
commodities meet contractual agreements.

Minimum Requirements:  
In order to quality for this position, you must possess a Masterâ&#8364;&#8482;s  
degree in pharmaceutical sciences, public health, or related field  
required with at least 5 years professional experience in developing  
countries. PharmD or Ph.D. in one of these degrees preferred. Minimum  
five years previous USAID grant or contract management experience  
required. Demonstrated technical competence in drug quality assurance  
and/or quality control.  
Knowledge, Skills, Abilities:  
Exceptional knowledge of malaria in developing countries.  
Understanding of drug development and FDA approval process for  
medicines.  
Experience in procurement of medicines for developing countries.  
Excellent verbal, written and presentation skills.  
Experience writing grants and identifying funding sources helpful.  
Strong negotiation, planning, and project management skills essential.

Demonstrated leadership and managerial skills.  
Ability to network with professionals from USAID, and other  
supranational organizations (WHO, PAHO, etc.) as well as local  
in-country representatives and government officials.  
Strong ability to work with nationals from varied backgrounds and  
cultures.  
Ability to travel at least 25% of the time.  
We are proud to be an EEO/AA employer.
