Scientist Job at US Pharmacopeia | Analytical Chemistry Job Apply Now
Are you looking for a Scientist job, Chemistry job, or Quality Control job that lets you contribute to global healthcare standards? Join the United States Pharmacopeia (USP) as a Scientist I in the Verification Program at Hyderabad. In this role, you’ll conduct analytical and quality control testing of dietary supplements and pharmaceutical ingredients, support data integrity, and ensure compliance with QMS documentation and GLP standards. This is your opportunity to make a meaningful impact on public health through science and precision.
About US Pharmacopeia
USP – United States Pharmacopeia is a global, science-based nonprofit organization dedicated to improving the quality and safety of medicines and healthcare products. Its Hyderabad center plays a crucial role in chemistry, scientific research, and quality control testing, supporting the global mission of strengthening public health. USP provides rewarding Scientist jobs and Chemistry jobs that emphasize innovation, compliance, and integrity. Through collaboration and scientific rigor, USP ensures that healthcare products meet the highest standards of safety and efficacy.
Job Details
- Job Title: Scientist I, Verification Program
- Location: Hyderabad, IND
- Req ID: SCIEN002975
- Qualifications: Master’s degree in Analytical Chemistry or Pharmacy.
- Experience: 1–3 years of experience in a pharmaceutical quality control or analytical testing laboratory.
Requirements
- Proficiency with HPLC (Empower software), Dissolution, and GC techniques.
- Knowledge of compendial methods (USP, BP, EP), ICH, and FDA guidelines.
- Strong QMS documentation and GLP compliance experience.
- Excellent problem-solving, communication, and teamwork skills.
Brief Job Overview
This Scientist job at USP Hyderabad offers the chance to apply your chemistry and quality control expertise in analytical testing. The Scientist I will perform laboratory analyses on dietary supplements and ingredients, interpret complex data, and maintain strict adherence to QMS documentation and GLP standards. The role requires a solid foundation in analytical chemistry and the ability to contribute to USP’s mission of advancing public health through scientific excellence.
Key Responsibilities
- Conduct quality control and analytical tests (HPLC, GC, Dissolution, ICP-MS, ICP-OES, wet analysis).
- Execute verification projects and maintain precise documentation.
- Prepare project reports and address QA feedback.
- Perform accurate data analysis and ensure regulatory compliance.
- Support ISO-9001 and ISO-17025 certifications, including internal audits.
- Collaborate with QA, HR, Purchase, and other departments.
- Ensure calibration, procurement, and proper maintenance of lab instruments.
- Maintain high standards of safety, accuracy, and QMS compliance.
- Support other analytical testing and verification programs as needed.
