Posted May 2, 2026
In this non-supervisory position at USP-India's NMR department, you will work on projects related to the characterization of molecules for synthetic chemistry, CDL, reference standard/ General Chapter development for Biologics, and Verification Labs. Your role as a Senior Scientist-I will involve supporting and monitoring a variety of non-routine and routine NMR tests, maintaining safety and GLP environment in the lab, including the evaluation of reference standards, development/validation of official methods, stability studies, and research projects in the NMR department. As part of USP's mission to advance scientific rigor and public health standards, you will contribute to increasing global access to high-quality medicines through public standards and related programs. Your responsibilities will include performing qNMR method development and validation to support the development of dRS, structure confirmation, and qNMR for the development of reference material. You will also review NMR sample analysis reports, prepare NMR reports, ensure project requirements are met, calibrate equipment, prepare/review lab reports and documents, and assist in safety projects impacting all USP Laboratory personnel. Additionally, you will promote Diversity, Equity, Inclusion, and Belonging principles at USP India. The ideal candidate for this role will have a background in Analytical Chemistry, Organic Chemistry, or M. Pharm with 10-13 years of experience in NMR or a Ph.D. with 7-10 years of experience in NMR. You must have hands-on experience in handling NMR instruments, be proficient in small molecule structure elucidation using NMR, and have exposure to GMP/GLP environments and documentation procedures. Expertise with Bruker NMR software, solid-state NMR, multinuclear NMR operations, and a comprehensive understanding of synthetic organic molecules and analytical chemistry are required. Strong communication skills, technical writing abilities, and familiarity with GMP/ISO-IEC 17025 Guidelines are essential. Desirable preferences include experience with biological molecules such as peptides, proteins, and vaccines, knowledge of General Chapter information, ELN, Empower, NuGenesis, and the ability to evaluate and interpret data. You should be skilled in anticipating, troubleshooting, and solving technical problems, demonstrate stakeholder collaboration experience, and have proven self-effectiveness skills. USP provides comprehensive benefits to protect you and your family, including company-paid time off, healthcare options, and retirement savings. Please note that USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. In this non-supervisory position at USP-India's NMR department, you will work on projects related to the characterization of molecules for synthetic chemistry, CDL, reference standard/ General Chapter development for Biologics, and Verification Labs. Your role as a Senior Scientist-I will involve supporting and monitoring a variety of non-routine and routine NMR tests, maintaining safety and GLP environment in the lab, including the evaluation of reference standards, development/validation of official methods, stability studies, and research projects in the NMR department. As part of USP's mission to advance scientific rigor and public health standards, you will contribute to increasing global access to high-quality medicines through public standards and related programs. Your responsibilities will include performing qNMR method development and validation to support the development of dRS, structure confirmation, and qNMR for the development of reference material. You will also review NMR sample analysis reports, prepare NMR reports, ensure project requirements are met, calibrate equipment, prepare/review lab reports and documents, and assist in safety projects impacting all USP Laboratory personnel. Additionally, you will promote Diversity, Equity, Inclusion, and Belonging principles at USP India. The ideal candidate for this role will have a background in Analytical Chemistry, Organic Chemistry, or M. Pharm with 10-13 years of experience in NMR or a Ph.D. with 7-10 years of experience in NMR. You must have hands-on experience in handling NMR instruments, be proficient in small molecule structure elucidation using NMR, and have exposure to GMP/GLP environments and documentation procedures. Expertise with Bruker NMR software, solid-state NMR, multinuclear NMR operations, and a comprehensive understanding of synthetic organic molecules and analytical chemistry are required. Strong communication skills, technical writing abilities, and familiarity with GMP/ISO-IEC 17025 Guidelines are essential. Desirable preferences include experience with biological molecules such as peptides, proteins, and vaccines, knowledge of General Chapter information, ELN, Empower, NuGenesi
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