Scientist I, Verification Program

As a Scientist at USP, your role will involve conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) utilizing suitable methods to enhance the laboratory's scientific proficiency and work ethic. You will offer extensive technical support and knowledge and provide valuable observations and insights into challenging projects. Your responsibilities will include: - Conducting 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 - Completing projects within designated timelines and priorities - Demonstrating a robust scientific approach to laboratory analysis - Utilizing personal experience, academic training, and technical insights to address complex technical issues - Compiling project reports and responding to QA observations - Executing all testing and data analysis with precision - Showing a strong commitment to continuous learning and personal development - Proposing and implementing new approaches or processes to enhance laboratory operations - Ensuring compliance with Good Laboratory Practices (GLP) and safety systems - Maintaining equipment calibration and coordinating the procurement of chemicals, glassware, etc. - Adhering to US Pharmacopeia (USP) mission, policies, and procedures - Supporting Global Public Health (GPH), Reference Standard Laboratory (RSL), and other departmental teams as required Qualifications required for this role include: - Masters degree in pharmacy or Analytical chemistry - Minimum 1 to 3 years of relevant laboratory experience - Previous engagement in a high-volume pharmaceutical manufacturing QC laboratory or a contract pharmaceutical analytical testing laboratory - Expertise in HPLC operation using Empower software and proficiency in dissolution analysis Additional Desired Preferences: - Proficiency in leading projects to completion with a high level of scientific expertise - Familiarity with compendial methods (USP, BP, EP, etc.) and pharmaceutical testing requirements - Experience in GC operation with Empower software, as well as proficiency in ICP-OES, ICP-MS, and LC-MS - Adept in operating and troubleshooting various analytical instrumentation - Exceptional communication and presentation skills - Familiarity with ICH guidelines and FDA regulations - Proficiency in Electronic Laboratory Notebook (ELN) As a non-supervisory role, you will contribute as an individual contributor to the laboratory's success. USP provides comprehensive benefits to protect yourself and your family, ensuring your personal and financial well-being is safeguarded. Apply now to join USP, an organization dedicated to developing quality standards for medicines, dietary supplements, and food ingredients to strengthen the supply of safe, quality products worldwide.,