Scientist I, Verification Program

**Description**

At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.

USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.

**Brief Job Overview**

This is non-supervisory role involves conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) utilizing suitable methods. The Scientist will enhance the laboratory's scientific proficiency and work ethic by offering extensive technical support and knowledge. Proficient in numerous common laboratory techniques, the Scientist is capable of providing valuable observations and insights into challenging projects. The individual in this role will furnish technical aid to the Verification Program by executing analytical tests and preparing comprehensive summary reports.

**How will YOU create impact here at USP?**

As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.

Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.- Conducts verification projects (Dietary Supplements/Dietary Ingredients) by performing individual analytical tests such as HPLC, GC,Dissolution, ICP-MS, ICP-OES, and wet analysis as assigned by the Team Leader- Completes projects within designated timelines and priorities.- Demonstrates a robust scientific approach to laboratory analysis.- Regularly utilizes personal experience, academic training, and technical insights, including emerging sciences, to address complex technical issues within the laboratory.- Compiles project reports and responds to QA observations.- Executes all testing and data analysis with precision, minimizing errors.- Shows a strong commitment to continuous learning and personal development.- Proposes and implements new approaches or processes to enhance laboratory operations.- Influences project direction positively by aligning own work with the overall direction of laboratory projects.- Assists with additional testing programs and laboratory maintenance tasks as required.- Ensures compliance with Good Laboratory Practices (GLP) and safety systems in the laboratory.- Maintains equipment calibration according to the schedule.- Coordinates the procurement of chemicals, columns, glassware, etc., in advance, in coordination with lab operations and the purchase department, considering project deadlines.- Adheres to US Pharmacopeia (USP) mission, policies, and procedures.- Cultivates positive relationships with Quality Assurance (QA), Human Resources (HR), Purchase, Accounting, IT, and other departments.- Participates actively in the preparation and planning for ISO-9001 & ISO-17025 certification/recertification, including taking an active role in internal QA and external audits and addressing audit issues promptly.- Supports Global Public Health (GPH), Reference Standard Laboratory (RSL), and other departmental teams as required for analytical testing, review, execution, and approval

**Who is USP Looking For?**- Master’s degree in pharmacy or Analytical chemistry.- Minimum 1 to 3 years with relevant laboratory experience.- Previous engagement in a high-volume pharmaceutical manufacturing QC laboratory or a contract pharmaceutical analytical testing laboratory, specifically pertaining to pharmaceutical dosage forms such as oral and liquid**Additional Desired Preferences**

**Supervisory Responsibilities**

None, this is an individual contributor role.

**Benefits**

USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind t