The U.S. Pharmacopeial Convention (USP) Technical Writer in Rockville, Maryland
Summary of the Position
The Technical Writer will support the Promoting the Quality of Medicines Plus (PQM+) program, a cooperative agreement between the United States Agency for International Development (USAID) and the United States Pharmacopeial Convention (USP), which aims to strengthen medical product quality assurance systems and improve the supply of quality-assured medical products in low- and middle-income countries. This position will coordinate with technical and field teams to develop high-quality written deliverables under the leadership of the PQM+ Sr. Technical Director.
This nonsupervisory position is responsible for ensuring that PQM+’s written products (i.e., gap assessments, lab SOPs, WHO PQ dossiers, regulatory guidelines) are technically sound, clearly written, and logically presented using text, tables and graphics. This position works closely with PQM+ headquarters technical staff and PQM+ field-based staff to produce products that comply with USAID, USP, and host-country branding requirements. This position will mentor technical staff on good writing practices and revise/edit text as needed to produce clear, clean deliverables. The successful candidate will bring deep expertise in technical writing and regulatory and manufacturing best practices to support this rapidly expanding global health program.
Roles and Responsibilities
Manages the PQM+ technical document preparation and review process
Working closely with team members (subject matter experts) to revise and author clear, concise, consistent, and technically accurate documents, including, but not limited to: SOPs, gap assessments, national guidelines, and training materials.
Support PQM+’s technical and field office teams to create high-quality written content to meet client needs, on schedule and on budget.
Creates or works with graphic designers to create diagrams, charts, and other visual aids to assist readers in understanding a product or process.
Coordinates with PQM+ Editor and Sr. Communications Manager to develop an editorial schedule to support overall program goals.
Determines the type of publication that will best serve the project requirements.
Consults with technical team members to learn about specific products or processes.
Assesses the client (e.g., donors, government agencies) needs for whom the technical and procedural documentation is intended; adjusts tone and technical terms used to meet those needs and to ensure understanding.
Collaborate with cross-functional global teams.
Resolve more complex situations by applying demonstrated knowledge and skills.
Prioritize projects in a fast-paced environment.
Performs other related duties as assigned.
Bachelor’s degree in English, technical writing, or equivalent experience as a technical writer
Five (5) years of experience as a technical writer
Proven track record of successfully delivering succinct and easily understandable documents under tight deadlines.
Expertise in Microsoft Word, Excel and PowerPoint
Native English speaker and writer – or equivalent
Ability to work in a multi-cultural environment, with colleagues from different backgrounds and cultures, and with content written by non-native English speakers
USAID and/or international development experience
Ability to translate technical content into clear concepts for graphics
Pharmaceutical sector experience
Publication in peer-reviewed global health journals
USAID marking and branding experience
Ability to synthesize large quantities of complex technical information into a highly readable and concise narrative.
USP offers an impressive benefits package, including:
Generous paid time off – 15 paid holidays, 10 sick days and 15 vacation days per year to start
An annual 401(k) contribution, beginning after 1 year of service, of 10% of pay (base and bonus) every pay period that vests immediately
Comprehensive individual and family healthcare plans with affordable premiums and low annual deductibles.
The U.S. Pharmacopeial Convention (USP) USP is an independent scientific organization that collaborates with the world's top experts in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP brings together more than 1,100 talented professionals across five global locations to deliver its mission to strengthen the supply of safe quality medicines and supplements worldwide.
USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, veteran status, sexual orientation, gender identity or any other protected class. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)
Job Category Technical Programs
Job Type Full-Time