Scientist I, Verification Program

Role Overview: You will be responsible for conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods in a non-supervisory role. As a Scientist at USP, you will enhance the laboratory's scientific proficiency and work ethic by providing extensive technical support and knowledge. Proficient in various common laboratory techniques, you will offer valuable observations and insights into challenging projects, aiding the Verification Program by executing analytical tests and preparing comprehensive summary reports. Key Responsibilities: - Conduct verification projects on 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 - Complete projects within designated timelines and priorities - Demonstrate a robust scientific approach to laboratory analysis - Utilize personal experience, academic training, and technical insights to address complex technical issues within the laboratory - Compile project reports and respond to QA observations - Execute all testing and data analysis with precision, minimizing errors - Commit to continuous learning and personal development - Propose and implement new approaches or processes to enhance laboratory operations - Ensure compliance with Good Laboratory Practices (GLP) and safety systems in the laboratory - Maintain equipment calibration according to the schedule - Coordinate the procurement of chemicals, columns, glassware, etc., in advance, in coordination with lab operations and the purchase department - Adhere to US Pharmacopeia (USP) mission, policies, and procedures - Cultivate positive relationships with various departments within the organization - Participate actively in the preparation and planning for ISO-9001 & ISO-17025 certification/recertification - Support Global Public Health (GPH), Reference Standard Laboratory (RSL), and other departmental teams as required for analytical testing, review, execution, and approval Qualifications Required: - Master's 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, specifically pertaining to pharmaceutical dosage forms such as oral and liquid - Expertise in HPLC operation using Empower software and proficiency in dissolution analysis Additional Company Details: At USP, inclusivity and diversity are valued, and the organization is committed to fair, merit-based selection processes. The company provides reasonable accommodations to individuals with disabilities and upholds policies that create an inclusive and collaborative work environment. 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 invests in leadership and workforce development to create high-performing, inclusive teams through training in equitable management practices.,