Chemistry Jobs at USP | PhD Candidates Apply Now for the Scientist Position
Join the U.S. Pharmacopeial Convention (USP) as a Scientist III in the Reference Standard Laboratory (RSL) in Hyderabad. This full-time, non-supervisory role offers hands-on experience in analytical chemistry, supporting USP’s mission to enhance global public health by ensuring access to high-quality medicines. Ideal candidates will have strong expertise in HPLC, GC, and other analytical instrumentation, with a commitment to GLP standards and laboratory excellence.
- Job Post: Scientist III, RSL
- Location: Hyderabad, India
- Req ID: SCIEN002748
About the Company
USP is a global scientific nonprofit organization committed to public health by developing standards that ensure the quality, safety, and efficacy of medicines worldwide.
Role Overview
The Scientist III in the Reference Standard Laboratory (RSL) performs analytical testing and laboratory operations under GLP compliance. This non-supervisory role involves supporting collaborative testing, ensuring timely completion of projects, and maintaining laboratory safety and quality standards.
Key Responsibilities
- Execute collaborative testing and data analysis with precision.
- Support verification, GPH, PQM, stability, and other departmental teams.
- Prepare evaluation reports, SOPs, protocols, and technical documents.
- Perform calibration, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of instruments.
- Maintain chemicals, reagents, and laboratory equipment; handle purchase requisitions.
- Troubleshoot scientific issues and resolve laboratory challenges independently.
- Mentor and train junior team members.
- Participate in internal and external audits, ensuring GLP compliance.
Qualifications & Experience
- Ph.D. in Chemistry or a Master’s degree in Chemistry/Pharmacy.
- Ph.D.: 1–3 years relevant laboratory experience; Master’s: 6–8 years.
- Expertise in HPLC, GC, and other analytical instrumentation (Titration, IR, KF, UV, Thermal analysis, Elemental analysis).
- Proven track record in delivering projects on time and with high quality for APIs or finished formulations.
- Proficient in Empower software and data analysis tools.
- Strong understanding of GLP regulations and exposure to regulatory audits.
Additional Preferred Skills
- Knowledge of lab management systems, ERP, ELN, and QR coding.
- Hands-on experience with ICP-OES/MS, IC, LC-MS, GC-MS.
- Experience in analytical method development and validation.
- Familiarity with pharmaceutical stability studies and compendial methods (USP, FCC, NF).
- Awareness of ISO/IEC 17025 standards.
Supervisory Responsibilities: None
Benefits
USP provides comprehensive benefits, including company-paid time off, healthcare options, and retirement savings, ensuring personal and financial well-being.
How to Apply
Interested candidates should apply directly to USP through the official portal. USP does not accept unsolicited resumes from third-party recruitment agencies.
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