2015 USP Summer Internship Program
USP Food and Drug Informatics Database (Spectral Library)
As the leading global standard-setting organization for medicines, foods, and dietary supplements, USP is expanding and enhancing its activities to fight counterfeit and substandard food and drug substances and products, as well as its research and innovation capabilities.
USP Spectral Library Project is a new initiative to explore the feasibilities and establish an authoritative and comprehensive collection of spectral information and pertinent information on medicine, food and dietary supplement quality. USP Spectral Library can be a useful tool for regulatory authorities, law enforcement agencies, hospitals, pharmacies, manufacturers and distributors around the world.
Reference Standards Laboratory
The candidate will work closely with the early procedure evaluation group in the Reference Standards Laboratory (RSL) to evaluate analytical procedures for new monographs or modernization/harmonization of monographs in USP-NF. The candidate will also assist in the evaluation and qualification of USP reference standards and the continued suitability for use program. Duties include performing laboratory testing using analytical techniques such as Karl Fisher, UV-Vis, FTIR, liquid and gas chromatography, and NMR to analyze pharmaceutical active ingredients, excipients, dietary supplements, biologics, and food ingredients. The candidate will generate and analyze analytical data and spend most of his/her assignments working in the laboratory.
Healthcare Quality Standards
Assist in provision of drug information to support the Healthcare Quality Expert Committee. Assist in creating drug reviews and maintaining health informatics database to support the USP Medicare Model Guidelines classification of marketed drugs. Assist in the development of standards related to patient safety including, but not limited to electronic health records allergy/intolerance reporting, the content and format of screen display on electronic media used in healthcare, revisions to USP pictograms and other standards to improve health literacy, and research related to electronic environments that promote safe medication use. Other topics related to the National Quality Strategy may also be identified by the April 2015 Convention that may shape the agenda of the Expert Committee. Read about USP's Council of Experts and Expert Committees.
Seeking PharmD candidates with drug information experience, and preferably in the last two years of professional training.
The candidate will assist the Compounding Expert Committee’s work in developing compounded preparation monographs based on stability-indicating assays and stability studies conducted by contract analytical laboratories. They will assist in supporting the work of the Expert Committee in developing and revising practice and quality standards for compounding. Duties include evaluation of laboratory work, literature research and review, and participating in working meetings. The candidate will gain increased professional knowledge of pharmaceutical compounding including understanding the regulatory framework around compounding as well as greater insight into USP processes and standards development.
Over-The-Counter Medicines – Prioritization of Strategies for Developing Modern Quality Standards
Method Development Project-PQM
Internship Fast Facts
- Duration: 12 weeks, 37.5 hour work week
- Location: U.S. Pharmacopeia Headquarters is walkable from the Twinbrook Metro Station, and a short Metro ride from Washington, D.C.
- Dates: May 25, 2015–August 14, 2015
- Compensation: Participants receive an hourly rate for each hour worked. Interns are responsible for travel, housing, and living expenses.
- Application Deadline: February 3, 2015
- Contact: OnaLee Dougherty, Talent Acquisition Specialist, at email@example.com, for more information.
- Enhance appreciation and understanding of USP's activities in standards-setting, core compendial activities, and global public health
- Advance scientific and/or practice knowledge
- Contribute to USP's research and standards knowledge base in a tangible way
Eligibility and Requirements
Undergraduate sophomores, juniors, or seniors and graduate students majoring in chemistry, biology, biochemistry, or pharmacy are eligible. Graduate students in pharmaceutical sciences are also eligible.
You must have completed basic chemistry courses, including quantitative chemical analysis. International students must possess the appropriate visa. Applicants must demonstrate self motivation, independent work habits, excellent oral and written communication skills, computer competence, and an ability to apply education and experience.
- Resume or CV
- Academic transcript(s)
- Letter of recommendation
- Essay (no more than 300 words) describing your interest and aspirations in the pharmaceutical, quality of manufactured medicines, excipients, and healthcare quality standards sciences
Applications may be mailed to:
United States Pharmacopeial Convention
c/o OnaLee Dougherty
12601 Twinbrook Parkway
Rockville, MD 20852-1790, USA
Applications may be e-mailed to: firstname.lastname@example.org
Applications must be received no later than February 3, 2015. USP will contact applicants quickly following the deadline to schedule interviews.