US Pharmacopeia job vacancy in Hyderabad
US Pharmacopeia is a global nonprofit organization that sets public standards for medicines, food ingredients, dietary supplements, and healthcare products. USP plays a critical role in advancing quality and safety within the pharmaceutical industry by developing and maintaining trusted standards used worldwide.
Position Summary – Scientist III (CDL)
- Job Title: Scientist III, Compendial Development Laboratory
- Company: US Pharmacopeia
- Location: Hyderabad, Telangana, India
- Employment Type: Full-time
- Industry: Pharmaceutical Manufacturing / Quality Standards
- Seniority Level: Mid-Senior Level
This US Pharmacopeia job vacancy in Hyderabad offers a pivotal role for analytical scientists involved in method development and validation, supporting global quality standards for medicines.
Key Responsibilities
As Scientist III – CDL, you will:
- Plan, execute & validate analytical methods per USP/NF monographs and guidelines
- Maintain GLP (Good Laboratory Practice) and safety standards in all experiments
- Generate and document laboratory data, reports, and project plans
- Support monograph modernization and compendial development initiatives
- Work with analytical instruments such as HPLC, FT-IR and UV-Visible systems
- Ensure accurate data recording and compliance with documentation procedures
Required Qualifications & Experience
To qualify for this US Pharmacopeia job vacancy, candidates should have:
- Master’s degree in Chemistry, Pharmaceutical Sciences, or a related discipline
- 6–8 years of experience in analytical method development and validation
- Strong understanding of USP/NF monographs and analytical testing techniques
- Hands-on experience with analytical instruments including HPLC, FT-IR, and UV-Visible spectroscopy
- GLP/QA compliance experience and excellent data documentation skills
Why Join US Pharmacopeia?
This role offers:
✅ A chance to work on globally recognized compendial standards
✅ Exposure to cutting-edge analytical research in pharmaceuticals
✅ Opportunity to influence quality and regulatory outcomes
✅ Collaborative and inclusive work environment focused on scientific excellence
Skills That Make Candidates Stand Out
💡 Deep analytical method expertise
💡 Experience interpreting regulatory compendial requirements
💡 Ability to operate complex instruments with precision
💡 Strong writing and reporting skills
💡 Critical thinking and problem-solving abilities
How to Apply
👉 Don’t forget to include keywords such as analytical method development, HPLC, GLP, and pharmaceutical standards to strengthen your application.